Top Benefits
About the role
The Big Picture
The Staff Design Assurance Engineer will be responsible for providing quality support for New Product Introduction (NPI) projects, ensuring that all design and development processes comply with applicable regulations and standards. This role requires a deep understanding of design controls, risk management, and usability engineering within the medical device industry. This position works closely with cross-functional teams, including R&D, Regulatory Affairs, and Process Engineering, to ensure the successful launch of new products that meet the highest quality and safety standards.
Your Impact Through Innovation
- Ensure the effectiveness of design controls activities for NPI projects, ensuring compliance, with ISO 13485, MDSAP and other relevant regulatory requirements
- Ensure risk management files are developed and maintained throughout the product lifecycle, identifying potential risks, and ensuring appropriate mitigation strategies are implemented
- Collaborate with cross-functional teams to develop and execute quality plans for new products, leveraging clinical knowledge to guide device design and testing, and ensuring design verification, validation, and qualification activities are conducted as per established protocols and regulatory standards.
- Provides valuable quality input throughout the product development process and ensures compliance with applicable standards and regulations by thoroughly reviewing and approving design inputs, outputs, and Design History Files (DHF).
- Identify opportunities for process improvement within the design and development lifecycle, implementing best practices to enhance product quality and development efficiency.
- Apply data-driven problem-solving and statistical analysis to systematically identify and address quality issues for new product development, enhancing product reliability and safety.
- Champions a quality-first mindset that emphasizes patient safety and customer satisfaction throughout the NPI process.
Your Unique Expertise
Required Skills:
- Minimum Bachelor’s degree in a scientific or engineering discipline
- Minimum of 3 years’ experience in the medical devices industry
- Minimum of 1 years’ experience with NPI processes or in a direct design assurance position
- Knowledge of ISO 13485, ISO 14971, IEC 62366-1
- Experience with design controls, design inputs and outputs, and risk mitigation activities.
- Excellent analytical and communication skills (both written and oral).
- Excellent organization and time management skills.
- Proficient in MS Office.
Our Distinctive Edge
- Effortless commute: say goodbye to commuting challenges/hassles with our complimentary shuttles and subsidized transit options, making your journey to work a breeze.
- Work-life integration: Embrace a well-balanced work-life rhythm through our hybrid model and flexible hours, empowering you to thrive both personally and professionally.
- Making a difference: Be a force for good with one dedicated day off for impactful volunteering, supporting causes close to your heart.
- Nurturing your career: Propel your career forward with abundant opportunities for on-site training, workshops, and personal development.
- Rewards that count: Reap the benefits of our comprehensive rewards package, including tuition reimbursement and a health spending account.
- Unleash your spirit: Join a thriving workplace culture filled with employee-led clubs, campaigns, sports teams, and exhilarating activities – fostering camaraderie and fun.
Our Impact
Baylis Medical Technologies is a leader in the development and manufacturing of innovative medical devices in the fields of radiology and cardiovascular. Headquartered in Canada, the company also provides contract manufacturing services to some of the world’s leading medical device companies.
Baylis Medical Technologies is an equal opportunity employer and encourages applications from all qualified individuals.
Please inform us if you require any accommodations during the recruitment process.
Take the Leap
We are looking for talented individuals, like yourself, to join Baylis Medical Technologies and make a meaningful impact in the lives of patients. Be part of our mission to revolutionize patient care through cutting-edge technology and breakthrough solutions.
Are you ready to join us? Apply today and let’s shape the future of healthcare together!
Want an inside look at careers and life at Baylis? See all our current job opportunities here and follow us on LinkedIn!
While we thank all applicants, only those being considered for an interview will be contacted.
About Baylis Medical
Baylis Medical is a leader in the development and commercialization of innovative medical devices in the fields of cardiology and spine. Headquartered in Canada, and with offices world-wide, our clinical solutions have been Improving the Lives of People Around the World for over 30 years.
Top Benefits
About the role
The Big Picture
The Staff Design Assurance Engineer will be responsible for providing quality support for New Product Introduction (NPI) projects, ensuring that all design and development processes comply with applicable regulations and standards. This role requires a deep understanding of design controls, risk management, and usability engineering within the medical device industry. This position works closely with cross-functional teams, including R&D, Regulatory Affairs, and Process Engineering, to ensure the successful launch of new products that meet the highest quality and safety standards.
Your Impact Through Innovation
- Ensure the effectiveness of design controls activities for NPI projects, ensuring compliance, with ISO 13485, MDSAP and other relevant regulatory requirements
- Ensure risk management files are developed and maintained throughout the product lifecycle, identifying potential risks, and ensuring appropriate mitigation strategies are implemented
- Collaborate with cross-functional teams to develop and execute quality plans for new products, leveraging clinical knowledge to guide device design and testing, and ensuring design verification, validation, and qualification activities are conducted as per established protocols and regulatory standards.
- Provides valuable quality input throughout the product development process and ensures compliance with applicable standards and regulations by thoroughly reviewing and approving design inputs, outputs, and Design History Files (DHF).
- Identify opportunities for process improvement within the design and development lifecycle, implementing best practices to enhance product quality and development efficiency.
- Apply data-driven problem-solving and statistical analysis to systematically identify and address quality issues for new product development, enhancing product reliability and safety.
- Champions a quality-first mindset that emphasizes patient safety and customer satisfaction throughout the NPI process.
Your Unique Expertise
Required Skills:
- Minimum Bachelor’s degree in a scientific or engineering discipline
- Minimum of 3 years’ experience in the medical devices industry
- Minimum of 1 years’ experience with NPI processes or in a direct design assurance position
- Knowledge of ISO 13485, ISO 14971, IEC 62366-1
- Experience with design controls, design inputs and outputs, and risk mitigation activities.
- Excellent analytical and communication skills (both written and oral).
- Excellent organization and time management skills.
- Proficient in MS Office.
Our Distinctive Edge
- Effortless commute: say goodbye to commuting challenges/hassles with our complimentary shuttles and subsidized transit options, making your journey to work a breeze.
- Work-life integration: Embrace a well-balanced work-life rhythm through our hybrid model and flexible hours, empowering you to thrive both personally and professionally.
- Making a difference: Be a force for good with one dedicated day off for impactful volunteering, supporting causes close to your heart.
- Nurturing your career: Propel your career forward with abundant opportunities for on-site training, workshops, and personal development.
- Rewards that count: Reap the benefits of our comprehensive rewards package, including tuition reimbursement and a health spending account.
- Unleash your spirit: Join a thriving workplace culture filled with employee-led clubs, campaigns, sports teams, and exhilarating activities – fostering camaraderie and fun.
Our Impact
Baylis Medical Technologies is a leader in the development and manufacturing of innovative medical devices in the fields of radiology and cardiovascular. Headquartered in Canada, the company also provides contract manufacturing services to some of the world’s leading medical device companies.
Baylis Medical Technologies is an equal opportunity employer and encourages applications from all qualified individuals.
Please inform us if you require any accommodations during the recruitment process.
Take the Leap
We are looking for talented individuals, like yourself, to join Baylis Medical Technologies and make a meaningful impact in the lives of patients. Be part of our mission to revolutionize patient care through cutting-edge technology and breakthrough solutions.
Are you ready to join us? Apply today and let’s shape the future of healthcare together!
Want an inside look at careers and life at Baylis? See all our current job opportunities here and follow us on LinkedIn!
While we thank all applicants, only those being considered for an interview will be contacted.
About Baylis Medical
Baylis Medical is a leader in the development and commercialization of innovative medical devices in the fields of cardiology and spine. Headquartered in Canada, and with offices world-wide, our clinical solutions have been Improving the Lives of People Around the World for over 30 years.