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

Chemist, AD

APOTEX, North York, ON

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 With guidance of Scientist, Analytical Development, responsible for performing all activities in early development research, analytical method development and validation for new products, comprehensive testing of API and finished dosages, and preparation of regulatory submission documentation. Acts as a key member in the project working team.Job Responsibilities Prepares working plan for assigned projects and provides timeline to Scientific Leader. Develops stability indicative analytical methods for drug substance and finished product. Works with Scientific Leader to prepare analytical methods, validation protocols and technical reports. Performs validation of analytical testing procedure for drug substance and drug product including dissolution methods. Ensures analytical methods validation is conducted according to approved validation protocol in a timely manner with accuracy and precision in compliance of laboratory SOP and guidelines. Performs all analytical tests for drug substance, including assay, related compounds, identifications and wet chemistry for API evaluation. Performs all analytical tests for PE/PO samples, including assay, degradation products and dissolution. Performs all analytical tests for API releasing, including assay, degradation products, dissolution and physical testing. Conducts other tests required for dosage submissions. Conducts lab investigations for OOS and OOT results. With guidance of scientists, performs troubleshooting on complex issues with respect to the stability of drug substances and drug products. Documents and reports results as per established SOP’s. Provides technical support to other department for the issues related to the stability of drug substance and drug product or for the responses to requirements of regulatory agencies. Work as a member of a team to achieve all outcomes. Develops and maintain strong relationships within Analytical R&D to ensure that the projects are delivered on time. Participates in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GMP requirements. Ensures all instruments assigned with responsibility within group/department are well maintained. Demonstrates corporate values in the performance of the work and interactions with others. Performs additional related duties, as assigned, in accordance with job responsibilities and necessary departmental objectives. 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 Recognized post-secondary education in analytical chemistry, organic chemistry, pharmaceutical sciences, or related field. Knowledge, Skills and Abilities knowledge of the instrumentation such as HPLC, GC, spectrophotometer and dissolution apparatus. Wet chemistry and analytical bench techniques. Knowledge in HPLC method development and method validation. Knowledge of wet chemistry, analytical bench techniques, Window-based software, and automated data acquisition systems. Working knowledge of LIMS is an asset. Good written and verbal English communication skills. Experience BSc with 5 years or MSc with 4 years or PhD with 2 years’ experience in a pharmaceutical lab in an R&D environment. Chromatographic method development and validation. 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. **For any inquires on this posting please contact: [email protected]