QA Manager Third Party Manufacturing (TPM) EMEA

Are you an experienced Quality Assurance professional with a passion for pharmaceutical manufacturing supplier quality and continuous improvement

We are looking for a QA Manager Third Party Manufacturing (TPM) to join our EMEA Quality this role you will be responsible for managing quality activities across a portfolio of external manufacturing partners ensuring products are manufactured in compliance with regulatory requirements and the highest quality standards.

What youll do

As QA Manager TPM you will act as the key quality partner for assigned third-party manufacturing sites across the EMEA region. Your responsibilities will include:

• Leading quality oversight of external manufacturing partners (TPMs)

• Driving continuous quality improvement initiatives and remediation plans

• Managing quality performance monitoring quality reviews and supplier compliance

• Leading investigations CAPAs change controls and quality risk assessments

• Supporting GMP audits regulatory inspections and quality compliance activities

• Reviewing and maintaining Quality Technical Agreements

• Collaborating closely with cross-functional stakeholders including Operations Regulatory Affairs Science & Technology and Commercial teams

• Acting as QA Lead during product technology transfers validation activities and new product introductions (NPI)

What were looking for

We are seeking a proactive and solution-oriented quality professional who enjoys working in a dynamic international environment.

Qualifications:

• Bachelors degree in Pharmacy Biotechnology Microbiology Pharmaceutical Sciences or a related scientific discipline

• 58 years of experience within Quality Assurance Manufacturing Operations Technical Support or Pharmaceutical Engineering

• Strong knowledge of cGMP regulations and pharmaceutical quality systems

• Experience with pharmaceutical manufacturing ideally including sterile liquid solid dosage forms or APIs

• Proven ability to manage stakeholders and work across multiple functions

• Strong communication problem-solving and influencing skills

• Leadership experience is considered an advantage

Why join us

• Work in an international EMEA role with broad exposure to manufacturing sites and stakeholders

• Drive meaningful quality improvements that directly impact patient safety and product quality

• Collaborate with diverse teams across Quality Operations Regulatory Affairs and Technical functions

• Take ownership of strategic quality initiatives and technology transfer projects