Overview of salaries statistics of the profession "Pharmaceutical Production Supervisor in "

Title: Tig WelderLocation: Richmond HillType: Contract to perm (First 3 months on our agency payroll) Payrate: TBDShift: days or afternoonsReporting to: Shop ForemanAboutOur client is recognized on the global market as a leading manufacturer of solid dosage processing equipment - They designs and fabricates a broad product line of pharmaceutical, nutraceutical and confectionery equipment for coating, mixing, blending, granulating and drying. Our product range provides proven solutions through all capacity requirements - from small scale portable laboratory and R&D models through to high-volume continuous systems. Position Mission: A welder-fitter will be required to perform basic to medium complex tig welding, installation and repair of stainless-steel sheet metal products Mandate and Roles: Major ResponsibilitiesTig weld, install and repair sheet metal products according to drawings, product specifications and with guidance from a sheet metal mechanic fabricatorOperate manual welding equipment to join materialsInspect parts, products for conformance to specification using appropriate measuring equipment and make corrections as requiredRead, understand and work according to company policies and procedures and supervisor’s instructionsFabricate sheet metal products using shear, saw, drill and various other manual/power toolsFasten parts, seams, joints together with bolts, rivets, caulks metal drive clips and bondsTrim, file, grind, deburr, buff and smooth surfaces, seams and joints of assembled parts, using hand tools and portable power toolsFabricate jigs/fixtures to enhance work performancePerform daily safety checks and maintain equipment in good working orderMaintain good housekeeping practices within the work area and return all unused parts to inventoryIdentify material with job numberMaintain good material handling and storage practicesOn daily basis, record hours worked against project work numberWork in a manner which meets production schedules and budgetsWear safety equipment and work in a safe manner at all timesPerform and complete all inspections / testing and documentationPerform other duties as and when required

Our client is recognized as a global market leading manufacturer of solid dosage processing equipment that fabricates a broad product line of pharmaceutical products.Title:   Mechanical AssemblerLocation: Richmond Hill. ONType: Temp to Perm (First 3 months on agency payroll)Pay rate:  $25.00 to $30.00 per hourShift: Days (flexible for afternoon shift if required)Reports To: Mechanical Assembler SupervisorDepartment:  Manufacturing.Position MissionA mechanical Assembler/ Service will assemble a wide variety of electro-mechanical, Hydraulic and Pneumatic products, including sheet metal components. Will be called upon to provide onsite mechanic services as needed. Mandate and Roles: Major ResponsibilitiesPerform assembly, installation and repair of electro-mechanical products with minimal supervision.Determine project requirements including scope, sequences, equipment and methods according to blueprints, drawings and written or verbal instructionsProvide technical guidance and direction to lower level personnelInspect parts, products for conformance to specification using appropriate measuring equipment and make corrections as required.Read, understand and work according to company policies and procedures and supervisors instructions.Assemble, fit, install, prefabricated parts to form subassemblies, finished product, using hand and power tools.Position, align and adjust assemblies, parts for proper fit and assemblyPosition, align and adjust bearings, shafts, moving parts for proper fit and assemblyAttach, fasten assemblies, parts together using bolts, rivets, caulks, bonds or other joining techniques.Operate pump trucks, small cranes to transport or position larger parts.Trim, file, grind, deburr, and buff surfaces, seams and joints, using hand tools and portable power tools.Position, align, gaskets, seals, trim, insulation for proper sealFabricate products, parts using lathe, milling machine, drill, saw, punching nailing equipment.Perform daily safety checks and maintain equipment in good working orderMaintain good housekeeping practices within the work area and return all unused parts to inventory.Identify materials with job numberMaintain good material handling and storage practicesOn a daily basis, record hours work against project numberWork in manner which meets production schedules and budgetsWear safety equipment and work in safe manner at all timesPerform and complete all inspections and FAT testing and documentationPerform other duties as and when required.Perform on-site service calls as required and complete all necessary documentationPerform the function of shipper/ receiver as required.Additional Responsibilities include the following but is not limited to:To recommend solutions all matters pertaining to the successful operation of the Manufacturing Department as they relate to the flow of orders through the system. To recommend major capital expenditures for the addition and replacement of machinery and equipment to the shop foremen.Requirements Education Completion of high school diploma or equivalent.Experience:Demonstration of mechanical aptitude and/or three years’ experience of working in a mechanical assembly environment.Mechanical aptitude and the ability to provide quality on-site mechanical serviceGood organizational skillsPossess current DriversDegree of SupervisionUnder the direction of the Shop Foreman the employee will be expected to achieve minimum performance levels through their working tenure. These will be reviewed on an annual basis. To be considered SUCCESSFUL, the employee must have demonstrated their ability to meet or exceed the prescribed minimum levels.Level Three: Within 12 weeks - SOMETIMES demonstrates an understanding of job requirements - Normal supervisionLevel Four: Within 26 weeks - OFTEN demonstrates an understanding of job requirements - Minimum supervisionLevel Five: Within 52 weeks - ALWAYS demonstrates an understanding of requirements - No supervision.             Program/Decision Impact and Scope:    Ensure that their objectives are clearly aligned with the strategic priorities of the company and that all efforts are made towards achieving those objectives. Accountability is accomplished through persistence in achieving excellence, being fully engaged and committed and effectively communicating.    Attributes and AttitudesDemonstrated excellent client service skills and commitment to providing attention to detail and a high standard of quality workExcellent communication skills, both verbal and writtenAbility to work independently as well as part of a teamHigh degree of concentration in all aspects of workAbility to work within tight time constraintsStress related to meet deadlines or schedules. Pleasant, clean, safe working environmentGood people skills, especially when dealing with co-workers and managementWorking Conditions and Level of EffortThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.This individual understands respects and adheres to the workplace Health & Safety rules and regulations.This position will be working in manufacturing plant setting and therefore will be exposed to the hazards: noise, heat, dust, welders flash, moving machinery (ie. Forklifts), and acids which require the use of protective equipment.Physical Effort: Considerable                                      Physical Environment: Considerable                                       Sensory Attention: Considerable     

Referred applicants should not apply directly to this role.All referred applicants must first be submitted through Workday by a current Loblaw Colleague.Come make your difference in communities across Canada, where authenticity, trust and making connections is valued - as we shape the future of Canadian retail, together. Our unique position as one of the country's largest employers, coupled with our commitment to positively impact the lives of all Canadians, provides our colleagues a range of opportunities and experiences to help Canadians Live Life Well.At Loblaw Companies Limited, we succeed through collaboration and commitment and set a high bar for ourselves and those around us. Whether you are just starting your career, re-entering the workforce, or looking for a new job, this is where you belong. Here at Loblaw, we take pride and ownership in helping Canadians live life well. We’re looking for talented colleagues who are passionate about providing an exceptional shopping experience for our Pharmacy customers and delighting them every step of the way! We can offer progressive careers, comprehensive training, flexibility and a great benefits package! Come share our vision and passion in delivering a superior customer experience. Be a part of our growing Health & Wellness philosophy that includes: Pharmacy, Dietitian, Medical and Optical services.The role of the pharmacy technician is to aid the pharmacy in the production of prescriptions and provide optimal customer service. Participate actively in growing prescription and OTC sales.What you'll do- Receive customer prescriptions, gather all necessary information, ensure completeness of information- Maintain patient & drug information files- Check pharmaceutical products prepared by another regulated pharmacy technician or by unregulated pharmacy personnel- Confirm accuracy and completeness of pharmaceutical products prepared for release- Preparation of prescription labels, affixing prescription and auxiliary labels to prescription container- Reconciling accounts and collecting outstanding monies from patients where necessary- Retrieving, counting, pouring, weighing, measuring, mixing & reconstitution of medications- Price prescriptions, prepare receipts, invoices, letters, memos, & general filing- Stock medications and related supplies, rotate & monitor stock- Maintaining perpetual inventory system in Kroll- Maintain customer privacy & confidentiality What you’ll need:- Registered pharmacy technician certification and maintained registration with appropriate pharmacy association- High level of professionalism- Knowledge of professional discipline, technical specialties, related process- Ability to implement practical procedures of systems which are moderately complex- Leadership and organizational skills- Excellent customer service skills and ability to handle cash accurately- Experience with Kroll an asset- Respect for the confidential and individual rights of our customers- Ability to effectively communicate one on one and over the telephone with coworkers, supervisors, suppliers, physicians and customers If you want to join a fast-paced winning team and believe you can have an immediate impact, then we want to hear from you!Apply today!Our commitment to Sustainability and Social Impact is an essential part of the way we do business, and we focus our attention on areas where we can have the greatest impact. Our approach to sustainability and social impact is based on three pillars - Environment, Sourcing and Community - and we are constantly looking for ways to demonstrate leadership in these important areas. Our CORE Values - Care, Ownership, Respect and Excellence - guide all our decision-making and come to life through our Blue Culture. We offer our colleagues progressive careers, comprehensive training, flexibility, and other competitive benefits - these are some of the many reasons why we are one of Canada’s Top Employers, Canada’s Best Diversity Employers, Canada’s Greenest Employers & Canada’s Top Employers for Young People.If you are unsure whether your experience matches every requirement above, we encourage you to apply anyway. We are looking for varied perspectives which include diverse experiences that we can add to our team.We have a long-standing focus on diversity, equity and inclusion because we know it will make our company a better place to work and shop. We are committed to creating accessible environments for our colleagues, candidates and customers. Requests for accommodation due to a disability (which may be visible or invisible, temporary or permanent) can be made at any stage of application and employment. We encourage candidates to make their accommodation needs known so that we can provide equitable opportunities. Please Note:Candidates who are 18 years or older are required to complete a criminal background check. Details will be provided through the application process.

Job DescriptionAs part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.How will you make an impact?Ensure process equipment and machinery are maintained in good order under Good Manufacturing Practices (GMP) guidelines for maximum equipment uptime. Provide technical skilled support and guidance to site operations via specialized maintenance services on a timely basis.Shift schedule: 12 hours, Continental shift (Monthly rotation, days and nights)What will you do?Repair, rebuild, refurbish machinery and equipment utilizing milling machines, lathes and all machine shop hand tools by performing the following tasks:Perform general maintenance on production equipment such as: Fluid Bed Dryers, Film Coaters, Tablet Presses, Transfer Pumps, Vacuum Systems, Processing Vessels and auxiliary equipment.Maintain production equipment, auxiliary equipment and building maintenance, including operator training on equipment set up and operation.Arrange with Group Leaders and Production Supervisors to schedule equipment down time for maintenance within the Preventative Maintenance program timeframes.Schedule equipment availability to perform preventative maintenance on time, maintain accurate records according to Good Manufacturing Practice requirements.Participate in Operational meetings, Rapids, Root Cause Analysis (RCA), Environmental Health and Safety (EHS) and other as required.Document applicable work activities performed within a CMMS ProgramMaintain a safe working environment and report potential hazards.Perform alternating or rotating shift work as well as requirement to work during maintenance shutdowns.How will you get here?Education:High school diploma/General Educational Development (GED) Certificate is required CollegeLicensed to practice as Industrial Millwright requiredCertified Ontario Trades PersonExperience:Minimum 3 years industrial mechanic or equivalent maintenance experience, preferably in food, cosmetic or pharmaceutical industries.1 - 3 years millwright experience, preferred.Experience reading drawing and schematics.Maximo CMMS program experience preferred.Equivalency:Equivalent combinations of education, training, and relevant work experience may be considered.Knowledge, Skills and Abilities:Familiarity with Good Manufacturing Practices (GMPs) and Occupational Health and Safety Act (OHSA)Regulations. Proactive and organized approach to completing tasks timely and efficiently. Attention to detail and quality of work. Ability to deal confidently with inside and outside clients. Good working knowledge of electronics and pneumatics is desirable. Demonstrated computer proficiency with Microsoft Office programs. Proficiency with the English Language.Standards and Expectations:Follow all Environmental Health & Safety Policies and Procedures. Work harmoniously with fellow team members, modelling positive team principles and partnering to meet project and departmental objectives.Carry out all duties within strict compliance to Thermo Fisher Scientific quality systems SOP's and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Actively engage in and adhere to departmental systems in order to maintain a smooth and efficient workflow (visual management, scheduling systems, etc.). Be client and patient conscious at all times. Understand Key Performance Indicators and strive to improve the performance of the team by identifying areas for system improvements and engage in problem solving. Models positive thinking and is open to change, motivating the team to adapt to shifts in priorities and new ways of working. Proactively identify areas for improvement in the execution of procedures. Communicate risks to timelines of deliverables in a proactive manner. Consistently strives to improve skills and knowledge in related field.Physical Requirements:Position requires ordinary ambulatory skills and physical coordination sufficient to move about manufacturing/office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of up to 40 pounds; arm, hand and finger dexterity; visual acuity to operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Usually in a comfortable environment but with regular exposure to factors causing moderate physical discomfort from such things as dust, loud noise, bright lights, fumes or odour. Use of Personal Protective equipment is required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one global team of 100,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Apply today! http://jobs.thermofisher.com

Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionEurofins CDMO Alphora is looking for Supervisor, Operations to join our dynamic and growing team!Our organization is growing! We offer both entry level roles as well as roles for more senior candidates with relevant experience, to join our expanding drug substance/API manufacturing operation.WHO ARE WE?Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients. Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients -“API’s”) as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements. Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects. Our employees work in close concert with clients throughout the development process to achieve their program objectives. Eurofins CDMO Alphora Inc. is growing its state-of-the-art organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths. DescriptionEurofins CDMO Alphora is looking for a Supervisor to join our GMP manufacturing department who enjoys a fast-paced, team environment with the opportunity to not only help support the growth of our manufacturing unit but also the development of the team.The role supports the Operations Manager with leading the department to ensure that Business Unit objectives are met. The role is responsible for providing leadership to the department while adhering to current Good Manufacturing Practices (cGMP), Environmental Health and Safety (EHS) and Eurofins CDMO Alphora's practices.DUTIES AND RESPONSIBILITIES:Support the Operations team with the manufacture of complex bulk drug substances/API’s to supply pre-clinical, clinical and commercial requirements.Support the team with the execution of chemical processing operations following batch record instructions to ensure the successful completion of batches.Ensure the team works in accordance with Environmental, Health and Safety Procedures, Standard Operating Procedures, and Production Batch Records.Promote Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).Resource planning, facility planning, and budgetingQualificationsA minimum of a College Diploma or Degree>10 yrs experience in pharmaceutical/chemical manufacturing leading a team preferredGMP experience preferredSolid GDP experienceDemonstrated safety first mindsetProven leadership, with preference for experience developing Jr teamsTechnically strong and willing to work on the floor with the teamProficient written and verbal communication skillsSite: Mississauga/OakvilleAdditional InformationAt Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at www.eurofins.caWe thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.NO AGENCIES, CALLS OR EMAILS PLEASE

Job DescriptionAs part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.How will you make an impact?Oversee and manage daily execution in the processing departments activities at Whitby Region Operations ensuring that safety, quality, delivery, budgetary, and customer targets are met. Develop and manage a functional team of processing managers supervisors and other professionals to oversee activities within the various areas of processing to ensure that manufactured product is made to current Good Manufacturing Practice (cGMP) standards and on time and in full.What will you do?FinancialHire and maintain trained and cGMP compliant workforce to ensure department has the adequate resources to meet the master packaging schedule.Represent processing operations in site S&OP cycle, ensures department can meet demand expectations.Work with processing management team to ensure daily production outputs (e.g., output quantity, etc.) and efficiencies.Drive PPI (operational excellence) culture through department, ensures annual process improvement targets and commitments are met.Monitor costs to ensure optimum operating while maintaining production costs.Complete projects assigned by Management within established timelines.Prepare quotations for existing products and future prospective clients.Participate in annual budget creation and monthly tracking of costs.ColleaguesDevelop and implement a succession plan and career path for all key individuals.Clearly outline key staff roles and expectations, as required.Provide annual performance reviews to Department Managers Supervisors and any other direct reports.Ensure the necessary training is provided to the individuals such that they are able to excel in their position and to monitor the performance of those who require help or direction.Support cross training of individuals thus achieving a flexible work force, as required.Hire staff and administers performance improvement plans, up to and including termination when appropriate.Offer options and suggestions for process, capacity, client services and staff morale improvements.Promote a safe working environment, report potential hazards, and ensure all direct reports follow Environmental Health and Safety procedures.Select, develop, and evaluate colleagues to ensure the efficient operation of the function. Work with and advise colleagues on administrative policies and procedures.Quality and Quality ImprovementEnsure excellent product quality as demonstrated in downward trend of Quality Investigation Reports/Quality Deviation Reports (QIR/QDRs) through more awareness to issues and expectations and excellent root cause identification and elimination.Ensure responses to client, Good Manufacturing Practices, safety, and QIR follow-up actions are completed in a timely manner, as required.Assist in investigating and resolving technical issues.Monitor processes to ensure efficient operation (e.g., yields).Instill a culture of professionalism and respect for co-workers, clients, and the products with which we work.How will you get here?Education: Bachelor’s degree in engineering, Sciences, or related field.Experience: Minimum 10 years operations experience, in a pharmaceutical industry or other GMP environment.Minimum 5 years previous supervisory experience.Equivalency: Equivalent combinations of education, training, and relevant work experience may be considered.Knowledge, Skills, and Abilities: Proven ability to coach and develop staff as well as the technical ability to coordinate departmental business activities. Full knowledge of Good Manufacturing Practices requirements and pharmaceutical processing regulations. Strong leadership, team building and organizational skills. Excellent computer skills, including the ability to develop spreadsheets, presentations, and report. All hires, promotions, or transfers to this role may require formal approval of qualifications by site and/or corporate QA against local regulatory requirements for Good Manufacturing Practices compliance. Proficiency with the English language.Standards and Expectations: Follow all Environmental Health & Safety Policies and Procedures. Work collaboratively with fellow team members, modelling positive team principles and partnering to meet project and departmental objectives. Carry out all duties within strict compliance to Patheon quality SOPs and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Actively engage in and adhere to departmental systems in order to maintain a smooth and efficient workflow (visual management, scheduling systems, etc.). Be client and patient conscious at all times. Understand Key Performance Indicators (KPI's) and strive to improve the performance of the team by identifying areas for system improvements and engage in problem solving. Models positive thinking and is open to change, motivating the team to adapt to shifts in priorities and new ways of working. Proactively identify areas for improvement in the execution of procedures. Communicate risks to timelines in a proactive manner. Consistently strives to improve skills and knowledge in related field. Physical Requirements: Light physical effort and fatigue. Walks, sits, or stands for limited periods. May require occasional equipment operation including keyboard equipment. Lifts light items for limited duration. Typically located in a comfortable indoor area. There may be regular exposure to mild physical discomfort from factors such as dust, fumes or odours, temperature extremes, loud noise, strong drafts, or bright lights. Use of Personal Protective equipment may be required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator on occasionally.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one global team of 100,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Apply today! http://jobs.thermofisher.com

Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients. Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients -“API’s”) as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements. Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects. Our employees work in close concert with clients throughout the development process to achieve their program objectives. Eurofins CDMO Alphora Inc. is growing its state-of-the-art organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths.Job DescriptionYou possess a high degree of initiative and are a team player with excellent communication abilities. You are comfortable in a modern, state of the art laboratory and are proficient with HPLC, GC, KF and various wet chemistry techniques. Your attention to detail, a comprehensive understanding of cGMP, strong organizational skills with the ability to multitask and work in a fast-paced environment, make you the ideal candidate to become a member of our team.Description of Department:The Quality Control department plays a key role in ensuring Eurofins CDMO Alphora Inc.’s compliance with Current Good Manufacturing Practices (cGMP) to ensure the production of safe and efficacious pharmaceutical APIs on behalf of our clients and their patients. The Quality Department is responsible for providing analytical support for the API manufacturing plant including support of raw material and finished product release, in process control testing, cleaning verification and other investigations. You will be working collaboratively with a small, dedicated team of QC chemists. Teamwork, communication and individual responsibility are key requirements. This is an excellent opportunity to obtain experience in a pharmaceutical manufacturing setting and to work on projects related to all phases of the pharmaceutical product life cycle.Description of Major Job Responsibilities: Reporting to the Quality Control Supervisor.Responsibilities include but are not limited to:Testing of raw materials, in process controls, and final products in support of our cGMP manufacturing operations.Coordination of testing priority with operation staff and QC supervisor, review and reporting of results.Troubleshooting analytical and instrument performance issues as required.Responsible to identify OOS results and assist in their investigation.Performing calibration checks and performance verifications of laboratory equipment.Work neatly to maintain the laboratory in an organized state.Participate in general upkeep and maintenance of the laboratory.Perform other related duties as required.Instrumentation:HPLC, GC, GC/Headspace, IR, KF and wet chemistry techniques are core to the role, practical experience with these techniques is a requirement.Experience with GCMS, LCMS, Ion Chromatography or other techniques is an asset.QualificationsDiploma or degree in a related field (Chemistry is preferred) with a minimum of 3 years relevant experience in analytical laboratory analysis, preferably in a pharmaceutical or other regulated environment.Excellent documentation and communication skills.Excellent problem-solving, planning, and organizational skilled coupled with a strong attention to detail.Ability to work independently under minimal supervision.Additional InformationThis position is based in a laboratory environment; significant time spent standing at a bench or sitting in front of a computer is required.Lab supports a 24/5 operating plant. The ability to work rotating shifts is a requirement. Extra hours, weekends may be required. Shift and OT premiums are provided.Travel between buildings on campus may be necessary. Valid drivers licence and access to vehicle is preferred.Additional InformationAt Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at www.eurofins.caWe thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.NO AGENCIES, CALLS OR EMAILS PLEASE

Referred applicants should not apply directly to this role.All referred applicants must first be submitted through Workday by a current Loblaw Colleague.Come make your difference in communities across Canada, where authenticity, trust and making connections is valued - as we shape the future of Canadian retail, together. Our unique position as one of the country's largest employers, coupled with our commitment to positively impact the lives of all Canadians, provides our colleagues a range of opportunities and experiences to help Canadians Live Life Well.At Loblaw Companies Limited, we succeed through collaboration and commitment and set a high bar for ourselves and those around us. Whether you are just starting your career, re-entering the workforce, or looking for a new job, this is where you belong. Here at Loblaw, we take pride and ownership in helping Canadians live life well. We’re looking for talented colleagues who are passionate about providing an exceptional shopping experience for our Pharmacy customers and delighting them every step of the way! We can offer progressive careers, comprehensive training, flexibility and a great benefits package! Come share our vision and passion in delivering a superior customer experience. Be a part of our growing Health & Wellness philosophy that includes: Pharmacy, Dietitian, Medical and Optical services.The role of the pharmacy technician is to aid the pharmacy in the production of prescriptions and provide optimal customer service. Participate actively in growing prescription and OTC sales.What you'll do- Receive customer prescriptions, gather all necessary information, ensure completeness of information- Maintain patient & drug information files- Check pharmaceutical products prepared by another regulated pharmacy technician or by unregulated pharmacy personnel- Confirm accuracy and completeness of pharmaceutical products prepared for release- Preparation of prescription labels, affixing prescription and auxiliary labels to prescription container- Reconciling accounts and collecting outstanding monies from patients where necessary- Retrieving, counting, pouring, weighing, measuring, mixing & reconstitution of medications- Price prescriptions, prepare receipts, invoices, letters, memos, & general filing- Stock medications and related supplies, rotate & monitor stock- Maintaining perpetual inventory system in Kroll- Maintain customer privacy & confidentiality What you’ll need:- Registered pharmacy technician certification and maintained registration with appropriate pharmacy association- High level of professionalism- Knowledge of professional discipline, technical specialties, related process- Ability to implement practical procedures of systems which are moderately complex- Leadership and organizational skills- Excellent customer service skills and ability to handle cash accurately- Experience with Kroll an asset- Respect for the confidential and individual rights of our customers- Ability to effectively communicate one on one and over the telephone with coworkers, supervisors, suppliers, physicians and customers If you want to join a fast-paced winning team and believe you can have an immediate impact, then we want to hear from you!Apply today!Our commitment to Sustainability and Social Impact is an essential part of the way we do business, and we focus our attention on areas where we can have the greatest impact. Our approach to sustainability and social impact is based on three pillars - Environment, Sourcing and Community - and we are constantly looking for ways to demonstrate leadership in these important areas. Our CORE Values - Care, Ownership, Respect and Excellence - guide all our decision-making and come to life through our Blue Culture. We offer our colleagues progressive careers, comprehensive training, flexibility, and other competitive benefits - these are some of the many reasons why we are one of Canada’s Top Employers, Canada’s Best Diversity Employers, Canada’s Greenest Employers & Canada’s Top Employers for Young People.If you are unsure whether your experience matches every requirement above, we encourage you to apply anyway. We are looking for varied perspectives which include diverse experiences that we can add to our team.We have a long-standing focus on diversity, equity and inclusion because we know it will make our company a better place to work and shop. We are committed to creating accessible environments for our colleagues, candidates and customers. Requests for accommodation due to a disability (which may be visible or invisible, temporary or permanent) can be made at any stage of application and employment. We encourage candidates to make their accommodation needs known so that we can provide equitable opportunities. Please Note:Candidates who are 18 years or older are required to complete a criminal background check. Details will be provided through the application process.

About Apotex Inc. Apotex Inc. is a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 8,000 people worldwide in manufacturing, R&D, and commercial operations. Apotex Inc. exports to more than 100 countries and territories and operates in more than 45 countries, with a significant presence in Canada, the US, Mexico, and India. Through vertical integration, Apotex is comprised of multiple divisions and affiliates including Apotex Inc., focused on generics; Apobiologix, a division of Apotex Inc. focused on biosimilar development; Aveva, an affiliate of Apotex Inc. fully integrated global developer and manufacturer of complete transdermal solutions; Apotex Consumer Products, a division of Apotex Inc. focused on brand name products; and Global Active Pharmaceutical Ingredients (GAPI), a division of Apotex Inc. focused on the manufacturing of active pharmaceutical ingredients (API) for Apotex and third parties. For more information visit: www.apotex.com. Job Summary The Technician, Electrical role is a key production function, specializing in electrical troubleshooting, repairs, preventative maintenance, calibrations and GMP activities to ensure SISPQ and machine integrity. This role requires technical expertise in order to help train and teach proper operations procedures to ensure the longevity of the equipment and improve reliability through production project and maintenance activities. Job Responsibilities Develop, implement and maintain predictive and preventative maintenance programs and/or calibration programs on material handling/production/process/development equipment ensuring compliance with SISPQ. Initiate and execute production maintenance projects (execute OQ’s, electrical upgrades & improvements) to completion. Install, repair and maintain electrical, electronic equipment, instrumentation as well as computerised systems (HMI, PC’s, vision systems & network troubleshooting) related to production machinery and systems. Must be able to perform work to CSA and ESA standards. Capable of using electrical testing equipment to diagnose problems. Understand and practice proactive maintenance and contribute in correcting problems before they become downtime issues. Supply training and coaching on equipment when necessary. Able to travel for training if necessary. Take ownership and accountability for issues, working proactively to resolve. Work efficiently to maximize department goals of minimizing equipment downtime. Ensure issues, follow-up actions and /or resolutions are clearly communicated to peers, vendors, customers and supervisors. This information should be transferred at shift overlaps as well as during the shift. Be a team player, a positive contributor; be open to suggesting and implementing ideas to better the business. Assist with mechanical repairs as needed. Effectively use SAP maintenance module to search history, create work orders and find parts and ensure supporting documentation is prepared. Able to create and modify drawings, P&ID’s and schematics when required. Prepare and update standard operating procedures (SOP’s) and standard documents (SD’s). Works as a member of a team to achieve all outcomes. Performs all work in support of our Corporate Values of Pride, Accountability, Integrity and Diligence; Demonstrates strong and visible support of our values. Performs all work in accordance with all established regulatory and compliance and safety requirements. All other duties as assigned. Job Requirements Ontario Industrial Electrician license (442A) or Construction and Maintenance Electrician License (309A) is required for this role. Apotex will consider candidates who expect to be licensed within 3 months Experience troubleshooting electronic and electrical control systems in a manufacturing environment. An Electronics, or Electro-Mechanical Technician or Technologist Diploma would be a definitive asset. Experience programming and troubleshooting Allen Bradley SLC500 Programmable Logic Controllers using RS Logix500 software. Extensive Knowledge on Omron, Siemens Simatic 7, Klockner Muller, and Toshiba PLCs is a definitive asset. Strong organizational and interpersonal skills Self-motivated and willingness to learn new skills. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

Job DescriptionAs part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.How will you make an impact?Lead the Facility & Grounds team to ensure the Site (Interior & Exterior) and Property are maintained in a safe, compliant, and visually optimal appearance. Schedule, and oversee daily team activities to ensure timelines are met. Manage the engagement, performance, and development of team members. Continuously monitor areas to ensure Good Manufacturing Practices (GMP) and Safety Standards are met and adhered to. Ensure Preventative procedures are evolved to ensure optimum effectiveness of the PM program. Participate and support regulatory inspections.What will you do?Manage Team Performance:Communicate job expectations and lead daily team huddles to ensure On Time Delivery (OTD) and Right First Time.Plan, monitor and appraise job results for quality and efficiency.Plan and monitor team activities to increase efficiency and minimize over time.Prioritize Unplanned & Planned work with Maintenance Planner.Verify the qualifications of personnel and recommends training as needed; ensure all personnel have been adequately trained on equipment and procedures and that proper documentation practices are followed.Conduct Performance Management Process (PMP) with staff.Coach, counsel and manage employee performance.Lead PPI (continuous improvement) initiatives.Maintain Regulatory Compliance:Enforce regulations to ensure “license to operate”; the Facility, Grounds, and associated systems are kept and operated in a GMP and Statutory compliant state.Ensure all planned maintenance is according to the manufacturers’ recommendations and to an approved schedule.Adhere to all approved Standard Operating Procedures (SOPs).Ensure staff are trained and qualified for duties.Prepare for and participate as a Subject Matter Expert (SME) during regulatory audits.Lead the investigation process and ensure deviations are properly documented.Ensure CAPAs, deviations and follow up actions are completed within the required timeline.Ensure all reports adhere to EH&S rules and regulations and work in a safe manner.Participate and support regulatory inspections.Ensures Maximum Site Availability and Appearance:Ensure quality of work and that work is completed in a safe and efficient manner.Establish and adhere to routine monitoring of the Facility & Grounds for availability, functionality and appearance - continuously improve as identified.Champion proactive maintenance vs. reactive maintenance.Collaborate with plant/ production/ personnel to ensure first-line maintenance identified by operators, where applicable.Review work planning and scheduling with planner, inform the maintenance planner/ team leader of routine preventative maintenance requirements.Develop maintenance routines following the manufacturers’ and suppliers’ recommendations.Review and implement improvements to existing preventive and predicative maintenance programs for optimal effectiveness.Recommend procedural changes and efficiency improvements for maintenance activities.Establish, maintain and report on Key Performance Indicators that represent the performance of the maintenance systems and assets.Analyze systems for energy usage & and implement efficiency improvements.Maintain Documentation - Site, Property and Applicable AssetsPrepare/ Revise Standard Operating Procedures (SOPs)Participate in the Change Control process.Follows changes, review drawings/ documents and revises as necessary.Ensure Site logs and all Computerized Maintenance Management System (CMMS) data collected is accurate and complete.Schedule/ monitor/ coordinate project work and directs external contractors.Maintain Professional and Technical Knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, participating in professional societies.Promote a safe working environment, report potential hazards, and ensure all direct reports follow Environmental Health and Safety procedures.Select, develop, and evaluate staff to ensure the efficient operation of the function. Work with and advise staff on administrative policies and procedures.Perform alternating or rotating shift work (as required).How will you get here?Education:Licensed tradesman in either of the following fields: Mechanical, Electrical.Bachelor of Engineering or Science (B.Sc.) or equivalent would be an asset.Experience:Minimum 7 years previous facility services experience in pharmaceutical, cosmetic or food manufacturing industry - pharmaceutical experience preferred.Previous experience with building (interior & exterior) and property maintenance systems.Previous supervisor or team/group leader experience.Experience in the use of RCFA tools such as FMEA/FMECA, Cause Mapping and Ishikawa Charts etc.preferred.Experience in operating a 24/7 operation preferred.Equivalency:Equivalent combinations of education, training, and relevant work experience may be considered.Knowledge, Skills, and Abilities:Excellent knowledge of Good Manufacturing Practices and Workplace Hazardous Materials Information System (WHMIS). Sound judgment, decision making and trouble shooting skills. Sound knowledge of Safety standards and statutory requirements for facilities. Excellent communication skills as well as proven interpersonal abilities. Proficiency using Microsoft Office software applications (Word, Excel, PowerPoint) and CMMS. Data analysis, problem definition & solving skills. Knowledgeable in specific RCM and predictive maintenance tools (vibration analysis, thermography and infrared tools and techniques, lubrication, machinery alignment, etc.). Proficiency with the English language.Standards and Expectations:Follow all Environmental Health & Safety Policies and Procedures. Work collaboratively with fellow team members, modelling positive team principles and partnering to meet project and departmental objectives. Carry out all duties within strict compliance to quality systems SOP's and Good Manufacturing Practice (GMP). Maintain workspace in a clean and orderly fashion. Actively engage in and adhere to departmental systems to maintain a smooth and efficient workflow (visual management, scheduling systems, etc.). Be client and patient conscious at all times. Understand Key Performance Indicators and strive to improve the performance of the team by identifying areas for system improvements and engage in problem solving.Models positive thinking and is open to change, motivating the team to adapt to shifts in priorities and new ways of working. Proactively identify areas for improvement in the execution of procedures. Communicate risks to timelines in a proactive manner. Consistently strives to improve skills and knowledge in related field.Physical Requirements:Position requires ordinary ambulatory skills and physical coordination sufficient to move about manufacturing/office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of up to 40 pounds; arm, hand and finger dexterity; visual acuity to operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Usually in a comfortable environment but with regular exposure to factors causing moderate physical discomfort from such things as dust, loud noise, bright lights, fumes or odour. Use of Personal Protective equipment is required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one global team of 100,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Apply today! http://jobs.thermofisher.com

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com. Job Summary Manufactures product as per patient, customer and company requirements while working within a team environment. Responsible and accountable for executing all manufacturing activities of the Batch Manufacturing Records (BMaRs), manual and automated Clean in Place process and Steam in Place process. Perform manual cleaning of all compounding equipment and manufacturing rooms as per associated standard operating procedures. Implement all department requirements as directed by the Dept. Supervisors, while following all S.W.P, G.M.P.’s, S.O.D.’s and Company policies/ regulations and remains aligned to the Apotex Strategic Objectives. Understanding of Good Manufacturing Practice and Standard Operating Procedures. Possess multi-tasking skills to achieve daily compounding schedule. Must be able to work independently as well as in a team environment. Performs all work in support of our Corporate Values of Collaboration, Courage, Perseverance and Passion; Demonstrates strong and visible support of our values. Shift- 11:00 pm to 7:00 am (Sunday to Thursday) or (Tuesday to Saturday). Job Responsibilities Compliance: Perform all duties according to the SODs, GMPs and all other established safety standards and company policies Correctly complete all documentation as per SODs, GDP and GMP requirements Access Apotex intranet for the purpose of locating and utilizing relevant SODs, MSDSs, company policies and procedures Notify Production Supervisor in the event of a departure from procedure, product defect, safety incident or other non-conformance event observed Recommends amendments to existing SODs for improvements Participate in audits in order to promote a culture of department compliance Participate in incidents or non-conformance investigations to identify and correct root causes Ensure that company policies and regulations/procedures with respect to safety/quality compliance are implemented and followed Productivity and Equipment: Safely operate all required equipment and machinery including those used to manufacture, store, clean and transport production related assets Effectively process batches within specifications to meet department batch execution targets by ensuring optimal cycle time in support of schedule adherence Dismantle, clean, sanitize and assemble processing equipment according to established SODs to ensure GMP compliance and meet department changeover targets in support of reliability and productivity goals Prepare and control process unit for start-up, shutdown and demonstrates troubleshooting skills. Ability to adjust equipment, valves, pumps and process equipment for maintenance. Understands, operate automated systems (Clean In Place & Steam In Place) with the use of Human Machine Interface/Computerised control panels as per applicable procedures. Execute applicable SAP transactions accurately and in a timely manner. Identifies and helps eliminate potential barriers in an effort to reduce downtime Ensure the proper selection, care and use of tools, parts and equipment while performing all job related duties Provides assistance to Senior team members including set-up issues and investigations Provide process feedback to Technical Operations with respect to new products or current product improvements Teamwork: Show team work by assuming responsibility for team goal setting to contribute to team’s performance on a daily basis Actively seek and accept positive and constructive feedback from Senior team members Contribute to on-going team growth and success in support of team and department goals Communicate effectively both verbally and written, in English Identify Continuous Improvement (CI) and helps implement action steps to optimize and improve efficiency rates, changeover times and product quality for existing and new products Capacity to effectively execute processParticipate in department projects or initiatives and actively contributes in team meetings and other team-related activities by providing positive feedback for process improvement Work in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education Minimum High School diploma. Knowledge, Skills and Abilities Demonstrated ability to be a team player in a dynamic, fast phased manufacturing environment. Demonstrated ability to utilize computerised /automated systems, computer software packages including e-mail, Excel, Word Possess strong mechanical aptitude. Demonstrated ability to facilitate the exchange of information among the team during bulk manufacturing. Strong two way communication and listening skills. Understanding of cGMP and ability to work in accordance with all departmental requirements. Able to lift between 5 to 20 kg and must be able to bend, reach, push/pull mobile equipment, bulk tank for duration of shift. Experience Experience in the pharmaceutical manufacturing environment executing manufacturing instructions and using automated Clean In Place & Steam In Place systems is preferred. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com. Job Summary The Chemical Operator PO3 is responsible for supporting the production process of our active pharmaceutical ingredient (API) facility through set-up, operation, monitoring and cleaning of heavy equipment, including reactors, filters, dryers, mills and production facilities, used to mix and handle ingredients. Operators also record information and observations relating to the mixing process, troubleshoot issues with equipment and assist in process improvement initiatives and the work plan development process and procedures 12 hours Continental Rotating between (Day- 7:00 am to 7:00 pm) & (Night- 7:00 pm to 7:00 am) Job Responsibilities Responsible for setting up, carrying out and monitoring processing steps as assigned by the Senior Chemical Operators or Production Supervisor, ensuring quality work in a timely manner. Works in compliance with all departmental and company Health and Safety policies, SOPs, cGMP procedures and other governmental regulations. Accurately records data in a timely manner in production documents, under supervision Reports injuries, accidents or damaged equipment. Uses appropriate personal safety equipment and follows safety procedures. Responsible for ensuring that the production facility is maintained in a neat and tidy manner in accordance with departmental policy. Responsible for the cleaning and sanitation, using detergents and chemicals, of all production equipment and production areas, such as dryer rooms. In constant communication with the Senior Chemical Operators, Production Specialist or Production Supervisor, including reporting plant and equipment status, observations or problems. Responsible for reviewing new or updated departmental SOPs and attending required training sessions. “When assigned to work in a work centre different from the one they are assigned to, they must work in a support role, shadow an operator that is trained and knowledgeable in the procedures specific to that area. “ To arrive at work 15 minutes prior to shift and prepare for upcoming shift. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education Minimum high school diploma College Diploma or CET (chemical engineering technician) certification is strongly preferred Post-secondary degree in chemical engineering or chemistry is desirable Knowledge, Skills and Abilities Aptitude for mechanics. Basic computer skills (ex. MS Office) Strong verbal and written communication skills and good command of English language Able to multi-task in fast-paced, physically demanding environment A desire to work with team members to improve processes and product quality in a fast-paced, physically demanding environment. Willingness to comply with safety and quality regulations, including wearing protective equipment. Must meet physical requirements of the position, including walking, standing or sitting for extended periods, lifting heavy objects, climbing, crouching and operating tools and equipment. Must be flexible and able to work continential (rotating days and nights) 12-hour shifts Demonstrated continuous improvement mindset and knowledge of GMP requirements are assets Experience Prior experience working in an industrial, manufacturing environment (6 months minimum) Process chemistry experience is preferred At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

Referred applicants should not apply directly to this role.All referred applicants must first be submitted through Workday by a current Loblaw Colleague.Come make your difference in communities across Canada, where authenticity, trust and making connections is valued - as we shape the future of Canadian retail, together. Our unique position as one of the country's largest employers, coupled with our commitment to positively impact the lives of all Canadians, provides our colleagues a range of opportunities and experiences to help Canadians Live Life Well.At Loblaw Companies Limited, we succeed through collaboration and commitment and set a high bar for ourselves and those around us. Whether you are just starting your career, re-entering the workforce, or looking for a new job, this is where you belong. Here at Loblaw, we take pride and ownership in helping Canadians live life well. We’re looking for talented colleagues who are passionate about providing an exceptional shopping experience for our Pharmacy customers and delighting them every step of the way! We can offer progressive careers, comprehensive training, flexibility and a great benefits package! Come share our vision and passion in delivering a superior customer experience. Be a part of our growing Health & Wellness philosophy that includes: Pharmacy, Dietitian, Medical and Optical services.The role of the pharmacy technician is to aid the pharmacy in the production of prescriptions and provide optimal customer service. Participate actively in growing prescription and OTC sales.What you'll do- Receive customer prescriptions, gather all necessary information, ensure completeness of information- Maintain patient & drug information files- Check pharmaceutical products prepared by another regulated pharmacy technician or by unregulated pharmacy personnel- Confirm accuracy and completeness of pharmaceutical products prepared for release- Preparation of prescription labels, affixing prescription and auxiliary labels to prescription container- Reconciling accounts and collecting outstanding monies from patients where necessary- Retrieving, counting, pouring, weighing, measuring, mixing & reconstitution of medications- Price prescriptions, prepare receipts, invoices, letters, memos, & general filing- Stock medications and related supplies, rotate & monitor stock- Maintaining perpetual inventory system in Kroll- Maintain customer privacy & confidentiality What you’ll need:- Registered pharmacy technician certification and maintained registration with appropriate pharmacy association- High level of professionalism- Knowledge of professional discipline, technical specialties, related process- Ability to implement practical procedures of systems which are moderately complex- Leadership and organizational skills- Excellent customer service skills and ability to handle cash accurately- Experience with Kroll an asset- Respect for the confidential and individual rights of our customers- Ability to effectively communicate one on one and over the telephone with coworkers, supervisors, suppliers, physicians and customers If you want to join a fast-paced winning team and believe you can have an immediate impact, then we want to hear from you!Apply today!Our commitment to Sustainability and Social Impact is an essential part of the way we do business, and we focus our attention on areas where we can have the greatest impact. Our approach to sustainability and social impact is based on three pillars - Environment, Sourcing and Community - and we are constantly looking for ways to demonstrate leadership in these important areas. Our CORE Values - Care, Ownership, Respect and Excellence - guide all our decision-making and come to life through our Blue Culture. We offer our colleagues progressive careers, comprehensive training, flexibility, and other competitive benefits - these are some of the many reasons why we are one of Canada’s Top Employers, Canada’s Best Diversity Employers, Canada’s Greenest Employers & Canada’s Top Employers for Young People.If you are unsure whether your experience matches every requirement above, we encourage you to apply anyway. We are looking for varied perspectives which include diverse experiences that we can add to our team.We have a long-standing focus on diversity, equity and inclusion because we know it will make our company a better place to work and shop. We are committed to creating accessible environments for our colleagues, candidates and customers. Requests for accommodation due to a disability (which may be visible or invisible, temporary or permanent) can be made at any stage of application and employment. We encourage candidates to make their accommodation needs known so that we can provide equitable opportunities. Please Note:Candidates who are 18 years or older are required to complete a criminal background check. Details will be provided through the application process.

Referred applicants should not apply directly to this role.All referred applicants must first be submitted through Workday by a current Loblaw Colleague.Come make your difference in communities across Canada, where authenticity, trust and making connections is valued - as we shape the future of Canadian retail, together. Our unique position as one of the country's largest employers, coupled with our commitment to positively impact the lives of all Canadians, provides our colleagues a range of opportunities and experiences to help Canadians Live Life Well.At Loblaw Companies Limited, we succeed through collaboration and commitment and set a high bar for ourselves and those around us. Whether you are just starting your career, re-entering the workforce, or looking for a new job, this is where you belong. Here at Loblaw, we take pride and ownership in helping Canadians live life well. We’re looking for talented colleagues who are passionate about providing an exceptional shopping experience for our Pharmacy customers and delighting them every step of the way! We can offer progressive careers, comprehensive training, flexibility and a great benefits package! Come share our vision and passion in delivering a superior customer experience. Be a part of our growing Health & Wellness philosophy that includes: Pharmacy, Dietitian, Medical and Optical services.The role of the pharmacy technician is to aid the pharmacy in the production of prescriptions and provide optimal customer service. Participate actively in growing prescription and OTC sales.What you'll do- Receive customer prescriptions, gather all necessary information, ensure completeness of information- Maintain patient & drug information files- Check pharmaceutical products prepared by another regulated pharmacy technician or by unregulated pharmacy personnel- Confirm accuracy and completeness of pharmaceutical products prepared for release- Preparation of prescription labels, affixing prescription and auxiliary labels to prescription container- Reconciling accounts and collecting outstanding monies from patients where necessary- Retrieving, counting, pouring, weighing, measuring, mixing & reconstitution of medications- Price prescriptions, prepare receipts, invoices, letters, memos, & general filing- Stock medications and related supplies, rotate & monitor stock- Maintaining perpetual inventory system in Kroll- Maintain customer privacy & confidentiality What you’ll need:- Registered pharmacy technician certification and maintained registration with appropriate pharmacy association- High level of professionalism- Knowledge of professional discipline, technical specialties, related process- Ability to implement practical procedures of systems which are moderately complex- Leadership and organizational skills- Excellent customer service skills and ability to handle cash accurately- Experience with Kroll an asset- Respect for the confidential and individual rights of our customers- Ability to effectively communicate one on one and over the telephone with coworkers, supervisors, suppliers, physicians and customers If you want to join a fast-paced winning team and believe you can have an immediate impact, then we want to hear from you!Apply today!Our commitment to Sustainability and Social Impact is an essential part of the way we do business, and we focus our attention on areas where we can have the greatest impact. Our approach to sustainability and social impact is based on three pillars - Environment, Sourcing and Community - and we are constantly looking for ways to demonstrate leadership in these important areas. Our CORE Values - Care, Ownership, Respect and Excellence - guide all our decision-making and come to life through our Blue Culture. We offer our colleagues progressive careers, comprehensive training, flexibility, and other competitive benefits - these are some of the many reasons why we are one of Canada’s Top Employers, Canada’s Best Diversity Employers, Canada’s Greenest Employers & Canada’s Top Employers for Young People.If you are unsure whether your experience matches every requirement above, we encourage you to apply anyway. We are looking for varied perspectives which include diverse experiences that we can add to our team.We have a long-standing focus on diversity, equity and inclusion because we know it will make our company a better place to work and shop. We are committed to creating accessible environments for our colleagues, candidates and customers. Requests for accommodation due to a disability (which may be visible or invisible, temporary or permanent) can be made at any stage of application and employment. We encourage candidates to make their accommodation needs known so that we can provide equitable opportunities. Please Note:Candidates who are 18 years or older are required to complete a criminal background check. Details will be provided through the application process.

Referred applicants should not apply directly to this role.All referred applicants must first be submitted through Workday by a current Loblaw Colleague.Come make your difference in communities across Canada, where authenticity, trust and making connections is valued - as we shape the future of Canadian retail, together. Our unique position as one of the country's largest employers, coupled with our commitment to positively impact the lives of all Canadians, provides our colleagues a range of opportunities and experiences to help Canadians Live Life Well.At Loblaw Companies Limited, we succeed through collaboration and commitment and set a high bar for ourselves and those around us. Whether you are just starting your career, re-entering the workforce, or looking for a new job, this is where you belong. Here at Loblaw, we take pride and ownership in helping Canadians live life well. We’re looking for talented colleagues who are passionate about providing an exceptional shopping experience for our Pharmacy customers and delighting them every step of the way! We can offer progressive careers, comprehensive training, flexibility and a great benefits package! Come share our vision and passion in delivering a superior customer experience. Be a part of our growing Health & Wellness philosophy that includes: Pharmacy, Dietitian, Medical and Optical services.The role of the pharmacy technician is to aid the pharmacy in the production of prescriptions and provide optimal customer service. Participate actively in growing prescription and OTC sales.What you'll do- Receive customer prescriptions, gather all necessary information, ensure completeness of information- Maintain patient & drug information files- Check pharmaceutical products prepared by another regulated pharmacy technician or by unregulated pharmacy personnel- Confirm accuracy and completeness of pharmaceutical products prepared for release- Preparation of prescription labels, affixing prescription and auxiliary labels to prescription container- Reconciling accounts and collecting outstanding monies from patients where necessary- Retrieving, counting, pouring, weighing, measuring, mixing & reconstitution of medications- Price prescriptions, prepare receipts, invoices, letters, memos, & general filing- Stock medications and related supplies, rotate & monitor stock- Maintaining perpetual inventory system in Kroll- Maintain customer privacy & confidentiality What you’ll need:- Registered pharmacy technician certification and maintained registration with appropriate pharmacy association- High level of professionalism- Knowledge of professional discipline, technical specialties, related process- Ability to implement practical procedures of systems which are moderately complex- Leadership and organizational skills- Excellent customer service skills and ability to handle cash accurately- Experience with Kroll an asset- Respect for the confidential and individual rights of our customers- Ability to effectively communicate one on one and over the telephone with coworkers, supervisors, suppliers, physicians and customers If you want to join a fast-paced winning team and believe you can have an immediate impact, then we want to hear from you!Apply today!Our commitment to Sustainability and Social Impact is an essential part of the way we do business, and we focus our attention on areas where we can have the greatest impact. Our approach to sustainability and social impact is based on three pillars - Environment, Sourcing and Community - and we are constantly looking for ways to demonstrate leadership in these important areas. Our CORE Values - Care, Ownership, Respect and Excellence - guide all our decision-making and come to life through our Blue Culture. We offer our colleagues progressive careers, comprehensive training, flexibility, and other competitive benefits - these are some of the many reasons why we are one of Canada’s Top Employers, Canada’s Best Diversity Employers, Canada’s Greenest Employers & Canada’s Top Employers for Young People.If you are unsure whether your experience matches every requirement above, we encourage you to apply anyway. We are looking for varied perspectives which include diverse experiences that we can add to our team.We have a long-standing focus on diversity, equity and inclusion because we know it will make our company a better place to work and shop. We are committed to creating accessible environments for our colleagues, candidates and customers. Requests for accommodation due to a disability (which may be visible or invisible, temporary or permanent) can be made at any stage of application and employment. We encourage candidates to make their accommodation needs known so that we can provide equitable opportunities. Please Note:Candidates who are 18 years or older are required to complete a criminal background check. Details will be provided through the application process.

Job Number: 65656 Group: Magna Exteriors Division: Mytox Mfg. Job Type: Permanent/Regular Location: Woodbridge Work Style: About us We see a future where everyone can live and move without limitations. That’s why we are developing technologies, systems and concepts that make vehicles safer and cleaner, while serving our communities, the planet and, above all, people. Forward. For all. Group Summary The Magna Exteriors portfolio of products includes access systems such as liftgates, exterior trim, modular systems, front-end modules including fascia, active aerodynamic systems and other lightweight structural components for automotive, commercial truck and other industrial markets. Recognized globally as an innovator in all aspects of vehicle exteriors, Magna provides everything needed, from materials development and design through manufacturing and assembly, to help automakers create sleek, state-of-the-art vehicles across the world. About the Role Supervises the activities of production staff including temporary assignments. Schedules staff, issues disciplinary action if required, conducts performance appraisals and other employee relations matters. Reviews production levels to determine priority of production to ensure productivity targets are achieved. Monitors actual performance against targets and initiates corrective action to correct negative variances. Maintains efficiency and quality standards on production lines. Who we are looking for A driven leader to meet or exceed organizational goals by supporting team members to success. An excellent communicator, motivator and trainer. Site Benefits Employee engagement events and activities Quarterly bonuses Continuing education Training and development Your preferred qualifications • Physically capable of doing the job • Strong leadership skills and ability to motivate team members to meet targets • Proficient in English (verbal and written) and math • Computer literate - Microsoft programs - Word, Excel, PowerPoint, Outlook, Teams etc. • Ability to carry out instructions furnished in written, verbal or diagram form • Supervisor’s competency • Knowledge of all legislative requirements of the OHSA • Familiarity with CMI system and scheduling • Understanding of IATF 16949 requirements • Must have knowledge of the process and equipment in the assigned area • Knowledge of Time-and-Attendance Systems • Knowledge in WHMIS, Time & Attendance System (ADP), and Lock Out procedures • Good organizational skills, ability to work well without supervision • Ability to supervise and coordinate activities of production employees • Previous automotive production experience is an asset • Valid forklift license and ability to operate overhead crane • Knowledge of SPC Accommodations for disabilities in relation to the job selection process are available upon request. Your Responsibilities • Ensure that all required legislation is met. (i.e. OHSA, WHMIS) in his/her area • Perform workplace inspections • Be involved in accident/incident investigations and assist in a solution to prevent accidents from reoccurring • Responsible for required training of new and existing employees in his/her area and verification that the training was effective • Responsible for or assigning a competent designate, to train new and existing employees in standardized work • Responsible for or assigning competent designate to fill in for employee that may need to temporarily leave the line (i.e. bathroom break) • Ensure Layered Process Audits (LPA’s) are completed daily • Work cell production boards are being reviewed hourly at a minimum and actions are taken to correct and document any issues • Correct unsafe acts or conditions • Conduct performance appraisals and provide feedback when required • Carryout performance management when required • Coach and mentor line leaders • Responsible for allocation of manpower • Responsible for the flow of material and it’s components • Responsible for quality assurance for parts in their area as per the Inspection Instruction sheets • Handle Non-Conforming Material Report (NMR), corrective action or quality alert when defects are found in their area while keeping their area manager informed • Ensures equipment and productivity standards are realized • Review production schedules to ensure that daily customer requirements have been met • Review shift productivity, to ensure that standards have been achieved • Suggest changes/improvements to working conditions and use of equipment • Enter production results into the system • Review hours in T&A System and make corrections if needed • Prepares and approves weekly summary of hours worked for employees and delivers to HR for payroll processing • Must be able to work overtime when required and willing to help out when necessary as per customer demands • Lead and participate in Mytox Continuous Improvement and 5S activities • Enforces all Mytox safety rules and regulations using progressive discipline if required for subordinates • Conduct work area/work cell meetings • Maintains employee files • Performs all job functions abiding by the office/work standards, policies and procedures as outlines in the company handbook. • Performs all job functions in alignment with IATF 16949 quality management standards and ISO 14001 • Actively participates in continuous improvement • Maintain 5S standards in working environment • Attend training based on Mytox’s internal training matrix • Performs all job functions in a safe, healthful and environmentally conscious manner, abiding by all health, safety and environment rules and regulations as outlined in the company handbook • Performs other duties as assigned or any reasonable request by management. What we offer At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies. We invest in our employees, providing them with the support and resources they need to succeed. As a member of our global team, you can expect exciting, varied responsibilities as well as a wide range of development prospects. Because we believe that your career path should be as unique as you are. Awareness. Unity. Empowerment. At Magna, we believe that a diverse workforce is critical to our success. That’s why we are proud to be an equal opportunity employer. We hire on the basis of experience and qualifications, and in consideration of job requirements, regardless of, in particular, color, ancestry, religion, gender, origin, sexual orientation, age, citizenship, marital status, disability or gender identity. Magna takes the privacy of your personal information seriously. We discourage you from sending applications via email to comply with GDPR requirements and your local Data Privacy Law.

Job Number: 65654 Group: Magna Exteriors Division: Mytox Mfg. Job Type: Permanent/Regular Location: Woodbridge Work Style: About us We see a future where everyone can live and move without limitations. That’s why we are developing technologies, systems and concepts that make vehicles safer and cleaner, while serving our communities, the planet and, above all, people. Forward. For all. Group Summary The Magna Exteriors portfolio of products includes access systems such as liftgates, exterior trim, modular systems, front-end modules including fascia, active aerodynamic systems and other lightweight structural components for automotive, commercial truck and other industrial markets. Recognized globally as an innovator in all aspects of vehicle exteriors, Magna provides everything needed, from materials development and design through manufacturing and assembly, to help automakers create sleek, state-of-the-art vehicles across the world. About the Role Supervises the activities of production staff including temporary assignments. Schedules staff, issues disciplinary action if required, conducts performance appraisals and other employee relations matters. Reviews production levels to determine priority of production to ensure productivity targets are achieved. Monitors actual performance against targets and initiates corrective action to correct negative variances. Maintains efficiency and quality standards on production lines. Who we are looking for A driven leader to meet or exceed organizational goals by supporting team members to success. An excellent communicator, motivator and trainer. Site Benefits Employee engagement events and activities Quarterly bonuses Continuing education Training and development Your preferred qualifications • Physically capable of doing the job • Strong leadership skills and ability to motivate team members to meet targets • Proficient in English (verbal and written) and math • Computer literate - Microsoft programs - Word, Excel, PowerPoint, Outlook, Teams etc. • Ability to carry out instructions furnished in written, verbal or diagram form • Supervisor’s competency • Knowledge of all legislative requirements of the OHSA • Familiarity with CMI system and scheduling • Understanding of IATF 16949 requirements • Must have knowledge of the process and equipment in the assigned area • Knowledge of Time-and-Attendance Systems • Knowledge in WHMIS, Time & Attendance System (ADP), and Lock Out procedures • Good organizational skills, ability to work well without supervision • Ability to supervise and coordinate activities of production employees • Previous automotive production experience is an asset • Valid forklift license and ability to operate overhead crane • Knowledge of SPC Accommodations for disabilities in relation to the job selection process are available upon request. Your Responsibilities • Ensure that all required legislation is met. (i.e. OHSA, WHMIS) in his/her area • Perform workplace inspections • Be involved in accident/incident investigations and assist in a solution to prevent accidents from reoccurring • Responsible for required training of new and existing employees in his/her area and verification that the training was effective • Responsible for or assigning a competent designate, to train new and existing employees in standardized work • Responsible for or assigning competent designate to fill in for employee that may need to temporarily leave the line (i.e. bathroom break) • Ensure Layered Process Audits (LPA’s) are completed daily • Work cell production boards are being reviewed hourly at a minimum and actions are taken to correct and document any issues • Correct unsafe acts or conditions • Conduct performance appraisals and provide feedback when required • Carryout performance management when required • Coach and mentor line leaders • Responsible for allocation of manpower • Responsible for the flow of material and it’s components • Responsible for quality assurance for parts in their area as per the Inspection Instruction sheets • Handle Non-Conforming Material Report (NMR), corrective action or quality alert when defects are found in their area while keeping their area manager informed • Ensures equipment and productivity standards are realized • Review production schedules to ensure that daily customer requirements have been met • Review shift productivity, to ensure that standards have been achieved • Suggest changes/improvements to working conditions and use of equipment • Enter production results into the system • Review hours in T&A System and make corrections if needed • Prepares and approves weekly summary of hours worked for employees and delivers to HR for payroll processing • Must be able to work overtime when required and willing to help out when necessary as per customer demands • Lead and participate in Mytox Continuous Improvement and 5S activities • Enforces all Mytox safety rules and regulations using progressive discipline if required for subordinates • Conduct work area/work cell meetings • Maintains employee files • Performs all job functions abiding by the office/work standards, policies and procedures as outlines in the company handbook. • Performs all job functions in alignment with IATF 16949 quality management standards and ISO 14001 • Actively participates in continuous improvement • Maintain 5S standards in working environment • Attend training based on Mytox’s internal training matrix • Performs all job functions in a safe, healthful and environmentally conscious manner, abiding by all health, safety and environment rules and regulations as outlined in the company handbook • Performs other duties as assigned or any reasonable request by management. What we offer At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies. We invest in our employees, providing them with the support and resources they need to succeed. As a member of our global team, you can expect exciting, varied responsibilities as well as a wide range of development prospects. Because we believe that your career path should be as unique as you are. Awareness. Unity. Empowerment. At Magna, we believe that a diverse workforce is critical to our success. That’s why we are proud to be an equal opportunity employer. We hire on the basis of experience and qualifications, and in consideration of job requirements, regardless of, in particular, color, ancestry, religion, gender, origin, sexual orientation, age, citizenship, marital status, disability or gender identity. Magna takes the privacy of your personal information seriously. We discourage you from sending applications via email to comply with GDPR requirements and your local Data Privacy Law.

Job Number: 65657 Group: Magna Exteriors Division: Mytox Mfg. Job Type: Permanent/Regular Location: Woodbridge Work Style: About us We see a future where everyone can live and move without limitations. That’s why we are developing technologies, systems and concepts that make vehicles safer and cleaner, while serving our communities, the planet and, above all, people. Forward. For all. Group Summary The Magna Exteriors portfolio of products includes access systems such as liftgates, exterior trim, modular systems, front-end modules including fascia, active aerodynamic systems and other lightweight structural components for automotive, commercial truck and other industrial markets. Recognized globally as an innovator in all aspects of vehicle exteriors, Magna provides everything needed, from materials development and design through manufacturing and assembly, to help automakers create sleek, state-of-the-art vehicles across the world. About the Role Supervises the activities of production staff including temporary assignments. Schedules staff, issues disciplinary action if required, conducts performance appraisals and other employee relations matters. Reviews production levels to determine priority of production to ensure productivity targets are achieved. Monitors actual performance against targets and initiates corrective action to correct negative variances. Maintains efficiency and quality standards on production lines. Who we are looking for A driven leader to meet or exceed organizational goals by supporting team members to success. An excellent communicator, motivator and trainer. Site Benefits Employee engagement events and activities Quarterly bonuses Continuing education Training and development Your preferred qualifications • Physically capable of doing the job • Strong leadership skills and ability to motivate team members to meet targets • Proficient in English (verbal and written) and math • Computer literate - Microsoft programs - Word, Excel, PowerPoint, Outlook, Teams etc. • Ability to carry out instructions furnished in written, verbal or diagram form • Supervisor’s competency • Knowledge of all legislative requirements of the OHSA • Familiarity with CMI system and scheduling • Understanding of IATF 16949 requirements • Must have knowledge of the process and equipment in the assigned area • Knowledge of Time-and-Attendance Systems • Knowledge in WHMIS, Time & Attendance System (ADP), and Lock Out procedures • Good organizational skills, ability to work well without supervision • Ability to supervise and coordinate activities of production employees • Previous automotive production experience is an asset • Valid forklift license and ability to operate overhead crane • Knowledge of SPC Accommodations for disabilities in relation to the job selection process are available upon request. Your Responsibilities • Ensure that all required legislation is met. (i.e. OHSA, WHMIS) in his/her area • Perform workplace inspections • Be involved in accident/incident investigations and assist in a solution to prevent accidents from reoccurring • Responsible for required training of new and existing employees in his/her area and verification that the training was effective • Responsible for or assigning a competent designate, to train new and existing employees in standardized work • Responsible for or assigning competent designate to fill in for employee that may need to temporarily leave the line (i.e. bathroom break) • Ensure Layered Process Audits (LPA’s) are completed daily • Work cell production boards are being reviewed hourly at a minimum and actions are taken to correct and document any issues • Correct unsafe acts or conditions • Conduct performance appraisals and provide feedback when required • Carryout performance management when required • Coach and mentor line leaders • Responsible for allocation of manpower • Responsible for the flow of material and it’s components • Responsible for quality assurance for parts in their area as per the Inspection Instruction sheets • Handle Non-Conforming Material Report (NMR), corrective action or quality alert when defects are found in their area while keeping their area manager informed • Ensures equipment and productivity standards are realized • Review production schedules to ensure that daily customer requirements have been met • Review shift productivity, to ensure that standards have been achieved • Suggest changes/improvements to working conditions and use of equipment • Enter production results into the system • Review hours in T&A System and make corrections if needed • Prepares and approves weekly summary of hours worked for employees and delivers to HR for payroll processing • Must be able to work overtime when required and willing to help out when necessary as per customer demands • Lead and participate in Mytox Continuous Improvement and 5S activities • Enforces all Mytox safety rules and regulations using progressive discipline if required for subordinates • Conduct work area/work cell meetings • Maintains employee files • Performs all job functions abiding by the office/work standards, policies and procedures as outlines in the company handbook. • Performs all job functions in alignment with IATF 16949 quality management standards and ISO 14001 • Actively participates in continuous improvement • Maintain 5S standards in working environment • Attend training based on Mytox’s internal training matrix • Performs all job functions in a safe, healthful and environmentally conscious manner, abiding by all health, safety and environment rules and regulations as outlined in the company handbook • Performs other duties as assigned or any reasonable request by management. What we offer At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies. We invest in our employees, providing them with the support and resources they need to succeed. As a member of our global team, you can expect exciting, varied responsibilities as well as a wide range of development prospects. Because we believe that your career path should be as unique as you are. Awareness. Unity. Empowerment. At Magna, we believe that a diverse workforce is critical to our success. That’s why we are proud to be an equal opportunity employer. We hire on the basis of experience and qualifications, and in consideration of job requirements, regardless of, in particular, color, ancestry, religion, gender, origin, sexual orientation, age, citizenship, marital status, disability or gender identity. Magna takes the privacy of your personal information seriously. We discourage you from sending applications via email to comply with GDPR requirements and your local Data Privacy Law.

REPORTING The Production Manager reports to the Plant Manager. RESPONSIBILITIES & ACCOUNTABILITIES Leadership Provide leadership and support to production personnel and supervisors. Focus on development of supervisors. Leads by example and achieves results by communicating job performance expectations. Makes business, employee and financial decisions that will set us up for long-term success. Maintain constant communication with all internal and external stakeholder, including the support departments. Create leader standard work for themselves and provide support to the supervisors in creating theirs. Enhance and develop policies, procedures and service systems to meet the goals of the facility. Improve overall value stream and become a coach to teach value stream mapping to all the leaders. Safety Ensures a "safety first" culture in the plant and ensures all manufacturing operations are conducted in compliance with Health & Safety regulations. Ensures that supervisors hold employees accountable in the event of contraventions to our safety practices. Production The Production Manager is responsible for all manufacturing activities among all shifts at Toro Aluminum. Find ways to eliminate barriers and provide solutions to execute manufacturing processes while maintaining a safe work environment for all employees. Utilizes best practice knowledge to adapt and implement new methods, lean and continuous improvement practices for manufacturing operations. Makes data-base decisions, maintains and publishes KPI's that measure success of objectives and drives continuous improvement. Establish processes and expectations in meeting the KPI's set out by the Plant Manager. Address high-level production issues and ensure they are resolved and communicated to all shifts. In partnership with the Quality team, establish and maintain a level of quality consistent with customer expectations. Act as a liaison for Lean methodology and implementation in the plant. Ensures the creation and maintenance of a visual management system in the plant using huddle boards, kanban boards, etc. On a daily basis, report plant performance to management.Conducts regular plant audits and reviews and ensures action items are completed. Monitor departmental performance against goals to ensure that progress is being made, and that corrective action is taken if necessary. Improve production standards through time studies and other standard data development methods. Identify areas for waste reduction. In consultation with the Plant Manager, develop plant or process flow layouts to improve productivity. Create and maintain production and manufacturing documentation such as SOP;s Persuade staff to adopt and incorporate quality and CI methods into their work. Prepare operational schedules and coordinate manufacturing activities to ensure production and quality of products meets specifications. Engagement Drives a culture of high performance where everyone is committed to and accountable for delivery of performance goals.Engages the department stakeholders to ensure the success of the team.Formalize the job requirements, job descriptions and procedures for the supervisors and functions within the shop. Responsible for recruitment, hiring, terminations and performance management. Develop objectives/targets for the teams and hold them accountable. Manage manufacturing employees, line workers, and other staff; recommend optimal staffing levels and schedules. Identify relevant training needs and opportunities. Conduct a skills gap analysis and skills development plan. Implement and ensure the maintenance of the employee skills matrix. Manage the morale in the facility by setting and demonstrating a strong business ethic for dealing with employees. Adhere to and provide leadership in matters concerning the Bargaining Unit and the Collective Agreement. Plan for future production and staffing requirements. Ensure that company policies are being adhered to. Other Although this is a day shift role, the incumbent is expected to occasionally overlap with night and weekend shifts in order to properly support manufacturing efforts. The incumbent must be willing to spend one week on nights or weekends per month. Ensure ongoing compliance with local, national, and international standards and legislation. Other duties as assigned. REQUIREMENTS We are looking for employees who share in our core values. Do you emulate the following? Do what you say - We act with integrity so our customers trust us to deliver results Get it done - We find solutions to ensure we get the job done right Be better every day - We are passionate about improving our business, safety, and quality and we strive to be the best Think big picture - We think long-term, and investment in our business is critical to our success Build strong relationships - We value our employees, customers, suppliers, and advisors as an essential part of our business QUALIFICATIONS 5+ years of relevant experience as a Production Manager. Completion of University degree or College diploma. Demonstrate exceptional leadership, problem solving, coaching, technical skills and interpersonal skills. Must possess good verbal and written communication skills. Experience in lean methodology, quality and process improvements in a manufacturing environment. Strong analytical ability and detail orientation. Ability to influence others and effectively work in a team. Strong computer skills including Microsoft Office, Word, and Excel.

Title: Blow Molding Set-up Technician Location: Mississauga, ONType: Full Time Permanent Payrate: TBD + Premium + OTBenefits: Dental care, Extended health care, Life insurance, On-site parking, RRSP matchShift: Continental Night Shift {5,2,5.2)AboutOur client is a leading plastic manufacturer offering products from various manufacturing platforms including Injection Molding, Extrusion Blow Molding, Single and Two Stage Blow Molding, Two and Three Shot Precision Injection Molding, Aluminum Barrier and Plastic Barrier Laminate Tubes, Tin Tubes and Medical Device Inhaler Coatings. - They serve a broad range of markets and provide solutions for- Personal Care, Beverage, Food, Spirits, Household, Industrial, Pharmaceutical, Nutraceutical, Medical, Healthcare and more.The Role Set Up Technician is responsible to set-up production tooling, submit start up bottles to QA for approval to run, maintain / inspect tooling, test new products and perform repairs on equipment and machines where neededEducation/ Experience:Minimum 3+ years’ experience in injection stretch blow molding set upExperience on set up for Automa /SIPA, Nessei, Aoki ISBM machines and 2 stage SIDE machines is an assetPrior experience in plastic manufacturing requiredSecondary School diploma or equivalentFor safety and business purposes, must have communication skills including reading, writing and must be able to communicate to others as well as be able to receive communication from others in EnglishRequirements/Responsibilities:Understand the importance and impact of the quality policy while performing any/all aspects of the Set Up Technician designated duties including but not limited to the following:Set-up, maintain, test and perform repairs on equipment and machines.Provide process information to management so production equipment may be optimized and/or process corrected.Assist with training of personnel to perform various functions (i.e., assistant technicians, supervisors).Facilitate work flow and ensure product quality is maintained.Monitor machinery and process goals during shift and make adjustments as necessary to ensure optimum performance of processes.Diagnose and troubleshoot equipment malfunction and repair equipmentEnsure all documentations are complete in accordance with company policy and ISO 9001 quality management system standard requirementsBe safety and quality conscious at all times, and continuously follow all safety policies and procedures on the jobCommunicate with QA team regarding quality issuesUse good manufacturing practices to maintain hygienic security while working at a machine or within the facility and demonstrate good housekeeping practicesPerform all other duties as assigned by manager Ability to lift up to 50 poundsAbility to stand for up to 12 hours