What are the responsibilities and job description for the Quality Engineer II position at Redbock - an NES Fircroft company?
Quality Engineer II (12-month contract // North Haven, CT):
A leading medical device company is seeking a resource with experience supporting standard production quality activities.
W2 ONLY (unable to sponsor visa or work OPT)**********
Top 3 technical skills that are required for this role:
- Six Sigma / Process Improvement projects
- Validation (IQ/OQ/PQ)
- Corrective and preventive actions (CAPA/NCR)
Must Haves:
- Good communication and organization skills
- Exposure to working in fast-pace environment
Education Required: Bachelor’s of Science or equivalent
Years’ Experience Required: 2 years of Quality Engineering 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. Support process and equipment validation via IQ/OQ/PQ/TMV/PD/DOE.
Required Knowledge and Experience:
- Requires a University Degree and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.