Descripcion
Responsibilities may include the following and other duties may be assigned. 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.
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Requisitos - Requirements
Technical Skills:
- Experience reviewing and approving validation test plans, reports, and deviations
- Capable of performing statistical analysis to support validations and product release
- Experience in medical devices manufacturing.
- investigate and collaborate in the investigation of atypical events to support product disposition
- PFMEA
Education & Experience:
- Bachelor of Science in Engineering with 2 to 5 years of directly related experience
- Non-Standard Shift (Availability for 1st, 2nd, and 3rd Shift)
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