About this role
QA Systems Specialist at Grand River Aseptic Manufacturing, Inc.. Location: Grand Rapids, Michigan, United States. Role: managing systems, leading investigations, facilitating teams Requirements: Bachelors in life sciences or 4+ years related experience; knowledge of QA in pharma/biotech/medical device, cGMP and FDA guidelines required; data analysis, aseptic manufacturing, ASQ/Green Belt, CFR 820/ISO 13485 preferred. Category: Quality Assurance Seniority: Mid Level Certifications: asq, green belt Commitment: Full Time Workplace: Onsite Languages: English