Manufacturing Engineer

3 weeks ago

Seabrook, United States Katalyst Healthcares and Life Sciences Full time

Responsibilities: Understand client methods and procedures Using client templates and protocols Develop protocols to qualify and validate related software components. Work with QA to obtain review and approvals of work package Support execution of test script and develop Summary Reports Other duties as necessary Must have a four-year degree in a technical area, Minimum of 5 years related experience. Medical device protocol and validation experience & proficiency is a must. Be highly reliable and onsite with minimal remote work. Great communicator and team player collaborates well with various depts Documentation proficiency (Protocol & Validation reports, mfg procedures, drawings) Must have worked in a manufacturing environment with some experience with product and/or process development.- design I/O validation mechanical background is a plus. Medical device manufacturing experience desired. Design Transfer and plastic/molding experience is a plus.- Continuous Improvement Project, WL-Molding, Kalamazoo, MI Must be proficient in using Microsoft Suite. Bachelor's Degree in Technical Field Minimum of 5 years related experience.

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    1 month ago

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