Overview of salaries statistics of the profession "Biomedical Product Development Engineer in Canada"

WHAT TO EXPECT  Are you mechanically inclined and interested in developing unique products? Due to our rapid growth, we have openings in our product development team. We need bright, creative and technically inclined people to participate in the development of rubber tracks for the defense, agricultural, industrial and recreational sectors.Here's an overview of your tasks: Oversee the development of new products, from requirement to customer approval, while following the product development process (PDP)Collaborate with a multidisciplinary team to develop rubber track assembly components for our industry customersWork closely with our simulation and materials department in the development of new productsParticipate in the various stages of product validation and support testingWork in conjunction with all functions of the company to complete multiple projects simultaneously, while respecting quality, cost and deadlinesFollow up with customers on a regular basis and answer their questions regarding their product

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.Lonza Kingston is hiring a Product Development Engineer or Mechanical Engineer for our Kingston, ON location where we have cutting edge technology such as the Cocoon® Platform . The Cocoon® Platform is an automated, scalable, and functionally closed-process cell therapy manufacturing platform. The Cocoon® is used to manufacture multiple types of cell therapy with applications in oncology (i.e., CAR-T), regenerative medicine (i.e., HSCs, MSCs) and tissue engineering (i.e., orthopedics). The Product Development Engineer or Mechanical Engineer will be responsible for driving continuous improvements in the Cocoon® product line. The Product Development Engineer or Mechanical Engineer also ensures the mechanical design for the Cocoon® Platform can be sustained for manufacture and distribution within regulated markets, and that field defects are investigated and addressed at the design-level. Learn more at: https://pharma.lonza.com/technologies-products/cocoon-platform Key responsibilities: Improves product quality and reliability, manufacturing efficiency and production yields through product design modificationInvestigates product complaints and non-conformances, performs root cause analysis of failures, and proposes corrective actions in a timely fashionReviews existing product designs, identifies weaknesses, proposes and implements improvementsLeads collaborative and complex design updates and implementations of corrective actions and backlog features related to product design within a cross-functional teamCreates strategy for the verification of corrective designs, and participates in verification activitiesGenerates and reviews technical documentation including investigative pursuits, conceptual design, mechanical drawings, and technical reports, all within a ISO 13485 Quality Management SystemApplies a risk-based approach to product design activities using xFMEA methodology Key requirements: Bachelor's degree in an Engineering discipline such as Systems, Mechanical, Biomedical or similar path of study; Master's degree, preferred.Minimum of 5 years of experience with leading product design in a regulated industry; medical device or product design/manufacture field required.Must have an in-depth knowledge of manufacturing processes: machining, injection molding, 3D printing.Extensive understanding of CAD systems required - preferably SolidWorks.Design experience with a focus on Design for Manufacturing and Design for Assembly required.Must be able to demonstrate troubleshooting and problem solving skillsMust be organized and detail oriented, also having hands-on mechanical aptitude, including ability to use common shop tools and measurement equipment.Experience with technical leadership for projects with cross functional teams (Quality, Design Transfer and Manufacturing)Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.Lonza Kingston is hiring a Product Development Engineer or Mechanical Engineer for our Kingston, ON location where we have cutting edge technology such as the Cocoon® Platform . The Cocoon® Platform is an automated, scalable, and functionally closed-process cell therapy manufacturing platform. The Cocoon® is used to manufacture multiple types of cell therapy with applications in oncology (i.e., CAR-T), regenerative medicine (i.e., HSCs, MSCs) and tissue engineering (i.e., orthopedics). The Product Development Engineer or Mechanical Engineer will be responsible for driving continuous improvements in the Cocoon® product line. The Product Development Engineer or Mechanical Engineer also ensures the mechanical design for the Cocoon® Platform can be sustained for manufacture and distribution within regulated markets, and that field defects are investigated and addressed at the design-level. Learn more at: https://pharma.lonza.com/technologies-products/cocoon-platform Key responsibilities: Improves product quality and reliability, manufacturing efficiency and production yields through product design modificationInvestigates product complaints and non-conformances, performs root cause analysis of failures, and proposes corrective actions in a timely fashionReviews existing product designs, identifies weaknesses, proposes and implements improvementsLeads collaborative and complex design updates and implementations of corrective actions and backlog features related to product design within a cross-functional teamCreates strategy for the verification of corrective designs, and participates in verification activitiesGenerates and reviews technical documentation including investigative pursuits, conceptual design, mechanical drawings, and technical reports, all within a ISO 13485 Quality Management SystemApplies a risk-based approach to product design activities using xFMEA methodology Key requirements: Bachelor's degree in an Engineering discipline such as Systems, Mechanical, Biomedical or similar path of study; Master's degree, preferred.Minimum of 7 years of experience with leading product design in a regulated industry; medical device or product design/manufacture field required.Must have an in-depth knowledge of manufacturing processes: machining, injection molding, 3D printing.Extensive understanding of CAD systems required - preferably SolidWorks.Design experience with a focus on Design for Manufacturing and Design for Assembly required.Must be able to demonstrate troubleshooting and problem solving skillsMust be organized and detail oriented, also having hands-on mechanical aptitude, including ability to use common shop tools and measurement equipment.Experience with technical leadership for projects with cross functional teams (Quality, Design Transfer and Manufacturing)Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.Lonza Kingston is hiring a Product Development Engineer or Mechanical Engineer for our Kingston, ON location where we have cutting edge technology such as the Cocoon® Platform . The Cocoon® Platform is an automated, scalable, and functionally closed-process cell therapy manufacturing platform. The Cocoon® is used to manufacture multiple types of cell therapy with applications in oncology (i.e., CAR-T), regenerative medicine (i.e., HSCs, MSCs) and tissue engineering (i.e., orthopedics). The Product Development Engineer or Mechanical Engineer will be responsible for driving continuous improvements in the Cocoon® product line. The Product Development Engineer or Mechanical Engineer also ensures the mechanical design for the Cocoon® Platform can be sustained for manufacture and distribution within regulated markets, and that field defects are investigated and addressed at the design-level. Learn more at: https://pharma.lonza.com/technologies-products/cocoon-platform Key responsibilities: Improves product quality and reliability, manufacturing efficiency and production yields through product design modificationInvestigates product complaints and non-conformances, performs root cause analysis of failures, and proposes corrective actions in a timely fashionReviews existing product designs, identifies weaknesses, proposes and implements improvementsLeads collaborative and complex design updates and implementations of corrective actions and backlog features related to product design within a cross-functional teamCreates strategy for the verification of corrective designs, and participates in verification activitiesGenerates and reviews technical documentation including investigative pursuits, conceptual design, mechanical drawings, and technical reports, all within a ISO 13485 Quality Management SystemApplies a risk-based approach to product design activities using xFMEA methodology Key requirements: Bachelor's degree in an Engineering discipline such as Systems, Mechanical, Biomedical or similar path of study; Master's degree, preferred.Minimum of 7 years of experience with leading product design in a regulated industry; medical device or product design/manufacture field required.Must have an in-depth knowledge of manufacturing processes: machining, injection molding, 3D printing.Extensive understanding of CAD systems required - preferably SolidWorks.Design experience with a focus on Design for Manufacturing and Design for Assembly required.Must be able to demonstrate troubleshooting and problem solving skillsMust be organized and detail oriented, also having hands-on mechanical aptitude, including ability to use common shop tools and measurement equipment.Experience with technical leadership for projects with cross functional teams (Quality, Design Transfer and Manufacturing)Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

WHY JOIN THE TEAM? To directly contribute to the company’s success by innovating and continuously improving its products To take advantage of excellent professional development opportunities within a constantly growing company To be part of a dynamic and motivated team MAIN ROLES OF THIS POSITION Develop system components from design to production Develop the vision that will guide system development on upcoming platforms Work with the design, production, purchasing, quality assurance and manufacturing engineering teams as well as suppliers at the different stages of product development Contribute to setting performance criteria, developing validation plans for each system and ensuring plan execution Carry out studies, analysis and calculations to guide designer technicians and project developers in their work, based on general and specific technical parameters YOU WERE BORN FOR THIS JOB IF YOU… Hold a bachelor’s degree in mechanical engineering Are fluent in English and French (spoken and written) Are able to use the principles of mechanics, tolerancing and material resistance Are familiar with the operation and construction of mechanical systems for motor vehicles Know how to implement predictive calculation tools Have proven project management skills Have strong learning and adaptability skills Are a great collaborator and exceptional team player Are able to occasionally travel to our multiple manufacturing sites Are already a fan of BRP recreational products AT BRP, WHEN WE TALK ABOUT BENEFITS, WE GO ALL IN. Let’s start with a strong foundation — You want it, we have it: Annual bonus: we work hard, and we know it. This yearly thank you is our way to fuel your dreams. Generous paid time away: winding down is as important as creating the future of recreational products.   Pension plan: we want to make sure you’ll enjoy retirement; we’ve got you covered.  Collective saving opportunities: being part of BRP allows you to tap into the strength of our saving programs.  Industry leading healthcare: fully paid by BRP, this program is here for you, whatever happens, so you can focus on what matters. What about some feel good extras:  Flexible work schedule: balance is key to innovation, and we want to make sure you are at the top of your game with a schedule that will work for you.  Summer schedule: time flies at BRP, so we hit pause to enjoy it. Holiday season shutdown: between Christmas and New Year’s, we close our facilities and refill on good times. Educational resources: you love what you do, and we get you resources to stay cutting-edge, so we all win together. Discount on BRP products: what we build is amazing, freeing, revolutionary, and you're first in line for the experience. WELCOME TO BRP We’re a world leader in recreational vehicles and boats, creating innovative ways to move on snow, water, asphalt, dirt and even in the air. Headquartered in the Canadian town of Valcourt, Quebec, our company is rooted in a spirit of ingenuity and intense customer focus. Today, we operate manufacturing facilities in Canada, the United States, Mexico, Finland, Australia and Austria, with a workforce made up of close to 20,000 spirited people, all driven by the deeply held belief that at work, as with life itself, it’s not about the destination; It’s about the journey.  AN EXCEPTIONAL AREA! > #LI-SD1

About UsAbout Us: Cryos Technologies is a leader in the orthotics industry, dedicated to improving mobility and enhancing the quality of life for our clients. We specialize in the custom design of foot orthotics that meet a wide range of needs. Our commitment to excellence, innovation, and patient satisfaction sets us apart in the healthcare field. We are seeking a skilled Mechanical/Biomedical Engineer to join our dynamic team, focusing on the design and certification of cutting-edge medical devices.Job DescriptionAt Cryos Technologies, you will be responsible for the design, development, and certification of medical devices. You will work closely with a cross-functional team to bring new products from concept through to market. This role requires a blend of technical expertise and creativity to design and operate test apparatus, ensuring our products meet rigorous safety and effectiveness standards.Key ResponsibilitiesDesign and develop medical devices, focusing on user needs and regulatory compliance.Construct and operate specialized test apparatus for product testing and validation.Maintain documentation throughout the product development lifecycle to ensure compliance with ISO 13485 and FDA regulations.Collaborate with the quality assurance team to ensure devices are compliant with all regulatory standards.Continuously improve device designs based on test results and stakeholder feedback.QualificationsBachelor's degree in Mechanical or Biomedical Engineering or a related field.Minimum of 3 years’ experience.Strong understanding of mechanical systems and proficiency with CAD software.Experience in programing with Python or similar languages.Experience with the full lifecycle of medical device design and certification.Knowledge of ISO 13485, FDA, and other regulatory standards is beneficial but not required.Excellent problem-solving skills and the ability to work in a team environment.BenefitsCompetitive salary and benefits package.Opportunities for professional growth and development.A collaborative and innovative work environment.