Metric Bio
Business Development Lead | Metric Bio | CDMO & Clinical Supply
Title:
Director of Quality Assurance
Location:
Oregon, US - Onsite - relocation support is provided!
Context:
CDMO
About the job
***Candidates need to be based within the US for consideration***
Metric Bio are proud to be partnered with a PE-backed CDMO on the hunt for a Director of Quality Assurance to oversee QA operations, guide continuous improvement initiatives, and ensure the integrity of quality systems and documentation.
Responsibilities
Lead and develop QA team, driving quality culture and continuous improvement
Maintain quality systems, documentation, and validation activities
Manage investigations, CAPAs, audits, change control, and document control
Ensure compliance with cGMP, FDA, and EU requirements
Support internal/external audits and inspections
Report quality metrics and collaborate cross-functionally
Manage QA resources and support wider company initiatives
Ideal Profile
Strong GMP/aseptic expertise with experience in FDA/EU inspections
Influential communicator with strong analytical and problem‑solving skills
Proven leader able to manage multiple priorities and build strong relationships
Proficient with standard software tools
Education & Experience
Bachelor’s degree in a scientific discipline (advanced degree preferred)
10+ years of GMP Quality experience; 5+ years in QA leadership
If you meet the requirements - let's have a conversation.
Seniority level Director
Employment type Full-time
Job function Quality Assurance
Industries Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at Metric Bio by 2x
#J-18808-Ljbffr
Director of Quality Assurance
Location:
Oregon, US - Onsite - relocation support is provided!
Context:
CDMO
About the job
***Candidates need to be based within the US for consideration***
Metric Bio are proud to be partnered with a PE-backed CDMO on the hunt for a Director of Quality Assurance to oversee QA operations, guide continuous improvement initiatives, and ensure the integrity of quality systems and documentation.
Responsibilities
Lead and develop QA team, driving quality culture and continuous improvement
Maintain quality systems, documentation, and validation activities
Manage investigations, CAPAs, audits, change control, and document control
Ensure compliance with cGMP, FDA, and EU requirements
Support internal/external audits and inspections
Report quality metrics and collaborate cross-functionally
Manage QA resources and support wider company initiatives
Ideal Profile
Strong GMP/aseptic expertise with experience in FDA/EU inspections
Influential communicator with strong analytical and problem‑solving skills
Proven leader able to manage multiple priorities and build strong relationships
Proficient with standard software tools
Education & Experience
Bachelor’s degree in a scientific discipline (advanced degree preferred)
10+ years of GMP Quality experience; 5+ years in QA leadership
If you meet the requirements - let's have a conversation.
Seniority level Director
Employment type Full-time
Job function Quality Assurance
Industries Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at Metric Bio by 2x
#J-18808-Ljbffr