What are the responsibilities and job description for the Quality System Manager position at JCW Group?
A commercial pharmaceutical manufacturer is hiring a QMS Manager to lead core quality systems at its Northern Colorado site.
This is a high-impact leadership role where you’ll own and improve critical QMS functions including document control, change control, and complaint handling, while acting as a key point of contact for audits and regulatory inspections.
You’ll lead a team across document control and quality systems, support ongoing EDMS enhancements, and drive process improvement initiatives that directly impact compliance and operational performance.
Visa sponsorship supported (transfers preferred) | No C2C / third-party candidates
You should apply if you have the following experience:
- 8 years in a GMP-regulated environment (pharma, biotech, or medical device)
- 5 years of people management experience (including leading teams and/or supervisors)
- Strong experience with QMS systems (document control, change control, complaints, CAPA)
- Proven audit and inspection readiness experience (FDA, ISO, etc.)
- Hands-on experience with EDMS/eQMS systems (Veeva strongly preferred)