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Sr. Design Assurance Engineer - Medical Device
Job in
Fridley, Anoka County, Minnesota, USA
Listed on 2025-11-14
Listing for:
Resolution Medical, LLC
Full Time
position Listed on 2025-11-14
Job specializations:
-
Engineering
Quality Engineering, Biomedical Engineer
Job Description & How to Apply Below
Job Summary
The Senior Design Assurance Engineer is a quality engineer that directly supports medical device product development from concept through commercialization working with cross-functional development teams to establish and maintain the design control deliverables, risk management activities, and DHF compliance to ensure delivery of the highest quality product to the customer.
Essential Functions- Create and ensure on-time execution of Quality Plans for internal development, OEM-based, Clinical Product Development (CPDP), and design change projects and leading on-time completion of protocols, reports and assigned project deliverables
- Accountable for Design Verification and Validation planning and /or, including active cross-functional root-cause analysis investigation & resolution activities
- Lead Risk Management activities from product Concept through Commercialization
- Support design test and inspection method development, and lead method validation activities
- Ensure DHF content integrity, completeness, and regulatory / standards compliance; collaboratively communicating & resolving gaps
- Support and ensure internal & external audit responses and on-time product re-certifications
- Support and ensure the establishment of objective, measurable, discrete, and verifiable customer, and product requirements
- Support and ensure objective component specification definitions, supplied component sampling plan development, and vendor qualifications
- Provide support for biocompatibility and sterilization qualifications
- Develop and lead other team members and provide work direction as required
- May have 2-3 technicians assigned for inspection, testing and project support
- Performs other functions as required
- BS Industrial Engineering, Engineering or Business Degree
- 8-15 years of medical device experience in Quality Operations, or equivalent experience
- 1-3 years of direct or indirect supervisory experience preferred
Comprehensive understanding of FDA regulations, ISO 13485, ISO 14971
- Statistical and data analysis
- Supervisory, Solid Management and Strong Leadership experience
- Prolonged periods sitting at a desk and working on a computer
- Must be able to lift 25 pounds at times
- Must have manual dexterity
- Must have excellent hand-eye coordination
- Must wear gown, gloves, and ear protection if applicable
- Group health & welfare benefits:
Options for Medical, Dental and Vision insurance, Health Savings Account (requires participation in eligible medical plan), and Flexible Spending Accounts. - Company-paid benefits:
Employee Life Insurance & Accidental Death & Dismemberment (AD&D), Long Term Disability (LTD), Kavira (requires participation in medical plan). - Voluntary, employee-paid benefits:
Employee Supplemental Life & AD&D, Spouse and Dependent Life & AD&D, Short Term Disability (STD), Accident, Critical Illness, and Hospital Indemnity, Employee Assistance Program. - Flexible Time Off Program
- Paid Parental Leave
- Paid Holidays
- Benefits and incentive compensation may be subject to generally applicable eligibility, waiting period, contribution, and other requirements and conditions.
- The typical base pay range for this role is between $,000/year. Compensation will vary based on individual job-related knowledge, skills, expertise, and experience. This position is eligible for a discretionary annual incentive program driven by organization and individual performance.
- 401(k) Plan:
Company-provided Safe Harbor Contribution of 3% of eligible earnings.
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