May 22, 2022
Accentuate Staffing is partnering with a rapidly growing biotechnology company who is hiring for a Quality Engineer with a clearly demonstrated background in validation. This is a direct hire opportunity, offering competitive pay and annual bonus, working onsite. The ideal candidate has experience with In-vitro diagnostics, CAP/CLIA regulated laboratories and validation processes.
Responsibilities Master’s Degree preferred, Bachelor’s Degree in a Scientific or Engineering field is required.
7+ years of GMP regulated experience within the medical device or in-vitro diagnostics industry.
5+ years of experience as a Quality Engineer, leading the process for in-vitro diagnostics or medical device validations.
Clear knowledge of CLIA/CAP and ISO based lab requirements.
Requirements Responsible for the quality engineering efforts towards the validation and equipment management programs.
Provides technical support for all product development processes, especially in the...
Accentuate Staffing
Research Triangle Park, NC, United States
Full time