What are the responsibilities and job description for the Quality Engineer position at Connect Life Science?
Senior Quality Engineer
Medical Devices
Minneapolis, MN - On-Site Position
12 month Contract - Potential Permanent Position After
Competitive Hourly Rate
A well-known MedTech company in Minneapolis are hiring for a Quality Engineer to support their growing Medical Device portfolio and bolster their Quality team for the next year, with likelihood to extend or convert to full time employee following a successful project.
You will be responsible for the development, implementation, maintenance, and improvement of quality assurance processes. You will work closely with R&D, RA and Manufacturing to ensure product quality within the business.
What You’ll Be Doing
- Partner with manufacturing teams and contract manufacturers to support end-to-end quality engineering activities
- Own non-conformance, deviation and CAPA processes
- Lead and support cross-functional teams to resolve quality issues and drive continuous improvement
- Provide QMS guidance across the business
- Support inspections and validations for medical devices
- Create, review, and approve technical and quality documentation (e.g. DHF, DMR, ECOs)
- Lead audits and support risk management activities
- Drive supplier performance and process improvements
- Support internal and external QMS improvements, audits and ongoing compliance efforts
Qualifications
- Bachelor's degree or equivalent in Mechanical, Electrical, or Manufacturing Engineering or Life Sciences
- 5 years' of industry experience
- Strong knowledge of quality tools used in the industry
- Analytical and quantitative approach to problem solving
Salary : $100,000 - $140,000