What are the responsibilities and job description for the Quality Engineer II position at Redbock - an NES Fircroft company?
W2 Candidates ONLY - No C2C or 3rd Party Arrangements
A globally distinguished medical device company is seeking a Quality Engineer II to support production related quality activities, including review and investigation of nonconformances and completion of CAPA activities to develop a resolution.
Strong candidates will have previous experience conducting TMV activities and Risk Management (PFMEAs). Ideal candidates will have strong experience with manufacturing process control plans and process capability assessment. Past experience with development or improvement of manufacturing lines and inspection processes will be preferred.
Quality Engineer II (6 month contract // Lafayette, CO):
Top 3 Skills:
- Manufacturing experience in a highly regulated industry
- Risk management in a highly regulated industry
- Test Method and/or MSA experience
Primary Responsibilities:
- Drawing and specification reviews
- Manufacturing process control plan reviews
- Measurement System Analysis (MSA), Test Method Validation (TMV) reviews
- Manufacturing process validation reviews
- Manufacturing process capability assessment
Education Required: Bachelor's degree in Engineering, Science, or technical field required
Years’ Experience Required: Minimum of 2 years of highly regulated industry experience.
Duties:
- 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.
Salary : $35 - $45
