Sr. Design Assurance Engineer
AbbottAbout the role
JOB DESCRIPTION:
MAIN PURPOSE OF THE ROLE
Responsible for completing Design Assurance activities in new product development from concept through commercialization. Conduct risk assessment/management and provide support to the regulatory department in
demonstrating compliance to QSR and ISO 13485 Quality System. Participate in cross-functional teams to implement design controls, validate test methods, plan verification and validation activities and provide critical quality review of protocol and report content. May support non-conformances, CAPA investigations, health hazard analysis, complaint investigations or supplier change notification activities for CSI products.
Essential Duties and Responsibilities:
• Partner with product development engineering, clinical, marketing, regulatory, and others to assure appropriate
quality requirements are defined for the specific device application and target patient population
• Lead cross functional teams in completing risk assessment and risk management activities
• Facilitate assessment and testing of biocompatibility for new and sustaining products
• Support regulatory submission content and review for compliance to QSR/MDD/MDR regulations
• Participate as member of a product development team responsible for supporting activities required to ensure
quality of the design through compliance with design controls
• Collaborate with R&D to create, optimize and validate mechanical and analytical test methods
• Support translation of user needs into design inputs and outputs.
• Work with cross functional team to plan and conduct design verification activities, human factors and design
validation activities
• Work with cross functional team to assess impact of proposed supplier changes
• Use statistical tools to analyze data and make acceptance decisions
• Provide support to Post Market Surveillance group to ensure trends are being assessed for impact to product risk
• Ensure technical accomplishments and other testing are fully documented for reference and traceability through
company systems
Qualifications:
• 4 Year / Bachelor or Masters of Science Degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Chemical Engineering, Industrial Engineering or related technical discipline.
• Minimum 5 years of experience in medical device or pharmaceutical industry or any other regulated industry.
• Regulatory compliance awareness in 21 CFR 820, ISO 14971, ISO 13485.
• Design assurance experience in risk management and design controls.
• Technical skills and ability to provide solutions to a variety of technical problems of moderate scope and
complexity.
• Practical approach to Quality and a partnering style with colleagues in all functions in the business.
• Technical writing and presentation skills.
The base pay for this position is
$72,700.00 – $145,300.00In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Operations Quality
DIVISION:
AVD Vascular
LOCATION:
United States > Minnesota > St. Paul : 1225 Old Highway 8 NW
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 10 % of the Time
MEDICAL SURVEILLANCE:
Yes
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s