Auditing, GMP (Good Manufacturing Practices), ISO (International Organization for Standardization), Leadership, Maintain Compliance, Manufacturing, People Management, Quality Assurance, Quality Management, Sales Qualification, Vendor/Supplier Evaluation
Own the quality function end to end for a growing biosynthetics and xenograft manufacturer working to become a go-to partner in its category. This role sits at the center of building a strong quality culture at a site investing in its team.
Why you should apply
- Own ISO 13485 and ISO 22442 compliance end-to-end, with real authority over final release decisions
- Sit at the center of a quality culture-building effort at a site the company is actively investing in
- $90,000 to $105,000 base salary, plus annual bonus eligibility
- Health, dental, and vision coverage, plus paid time off and paid holidays
What you'll be doing
- Oversee ISO 13485 and ISO 22442 compliance across the site
- Manage GMP compliance and quality system oversight
- Sign off on final product release
- Lead supplier qualification and audits
- Serve as the site's IACUC liaison for live-tissue sourcing
About you
- Be able to do the job as described.
- 4+ years of management or supervisory experience in a manufacturing environment
- Associate's or bachelor's degree, or 6 years of manufacturing and quality experience in lieu of a degree
- 3+ years of leadership experience
- ISO 13485 Lead Auditor certification or equivalent auditing experience preferred
How to apply
We'd love to see your resume, but we don't need it to have a conversation. Email Cat at ccupo@jacobsmgt.com and tell me why you're interested. Or, if you do have a resume ready, apply here.