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.