Des Plaines, IL, USA

Job Description:

Must have experience with regulated Quality Systems, preferably with medical devices or Pharma, regulations ISO 13485:2021 or ISO:9001. 21 CFR 820.
Possibility for overtime up to 5 hours/ week.
Assures the quality of manufactured products and processes per standard operating processes (SOP) and GMP (Good Manufacturing Practices).
BS degree and/or 5+ years equivalent experience.