What are the responsibilities and job description for the Quality Manufacturing Engineer - Medical Devices position at Planet Pharma?
Job ID: 627451
Our client, a leading Medical Device company, is seeking an experienced Quality Manufacturing Engineer for its Plymouth, MN facility. See below for other details!
Top Skills Needed:
- Data driven problem solving
- Solid understand and application of regulatory requirements
- Site Transfers, Site Shutdowns
Main Day-to-Day Tasks:
- Heavy site transfer support - from strategy development to execution
- Day to day sustaining operations quality support
- Project Management to adequately manage transfer activities timeline
Responsibilities:
- Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
- Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
- Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
- Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
- Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
- May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
Requirements:
- Bachelor's Degree within an Engineering realm and 4 years of experience