QA Manager TPM, EMEA: Supplier Quality & Compliance

People in Science; Weesp; On-site; EUR 90,000 - 120,000; Full time

Job summary

People in Science is seeking a QA Manager Third Party Manufacturing (TPM) for the EMEA region. You will oversee quality at external manufacturing partners, interact with internal stakeholders, and drive continuous improvement across the portfolio.

The role requires a Pharm/Degree, 5–8 years of QA/manufacturing experience, strong cGMP knowledge, and fluent French and English. Occasional travel to France and other European sites is expected.

Qualifications

• Bachelor's degree in Pharmacy or related field.
• 5–8 years of QA/pharma experience.
• Fluent French and English, both written and spoken.
• Strong knowledge of cGMP and pharmaceutical quality systems.
• Experience with GMP audits and regulatory inspections.

Responsibilities

• Lead quality oversight of assigned third-party manufacturing partners.
• Monitor supplier quality and drive improvement initiatives.
• Develop remediation and CAPA plans.
• Manage quality reviews and compliance activities.
• Lead investigations, CAPAs, change controls, and quality risk assessments.
• Support GMP audits, regulatory inspections and other compliance activities.
• Review Quality Technical Agreements.
• Collaborate with Operations, Regulatory Affairs, and other teams.
• Lead quality during technology transfers and new product introductions.
• Ensure risks are identified and managed.
• Travel regularly to TPM sites in France and across Europe.

Skills

Quality Assurance

Supplier Quality

Continuous Improvement

CAPA Investigations

GMP Knowledge

Cross-functional

Communication

Leadership

Travel Ready

Regulatory Awareness

Education

Bachelor’s degree in Pharmacy or related field

Job description

People in Science is seeking a QA Manager Third Party Manufacturing (TPM) for the EMEA region. You will oversee quality at external manufacturing partners, interact with internal stakeholders, and drive continuous improvement across the portfolio.

The role requires a Pharm/Degree, 5–8 years of QA/manufacturing experience, strong cGMP knowledge, and fluent French and English. Occasional travel to France and other European sites is expected.