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Senior Quality Engineer
- Contract
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Senior Quality Engineer for a medical device company located in Warsaw, IN. The client is an award winning medical device company and is consistently at the forefront of medical innovation. This innovative company is seeking a Senior Quality Engineer to assist on a new compliance project to have all client documentation requests completed and stored properly in regard to the EU MDR initiative.
Skill and Requirements:
- 5-10 years of experience in the Medical Device industry
- Experience with Design History Files (DHF) and Design History Requirements (DHR)
- Experience with Gauge R&R
- GD&T experience in a medical device environment
- Understanding of PFMEA
- Understanding and experience with control and inspections plans
- Knowledge of flow charts
- Strong Communicator
- Driven and proactive
This position is moving very quickly so please apply now for immediate consideration.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Clare Bogart at (+1) 224-236-4795 or upload your resume on our website - www.proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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#QA
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