Candidate will be responsible for the review, interpretation and trending of data from chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples in accordance with current Good Manufacturing Practices, SOP’s, compliance guidelines of the FDA and other regulatory bodies, and approved license requirements.  Candidate will schedule all group activities, personnel management, training and support, and coordinate testing priorities with other departments.  Candidate will also conduct performance management and development, including performance reviews and objectives, interviewing and hiring. 

Bachelor’s degree in related science field with 6+ years of experience in the medical device, biotech or pharmaceutical industry, advanced degree preferred.  At least 4 years of supervisory experience preferred.