Third Party Manufacturer and Technical Transfer QA Manager- EMEA

Key information

  • Publication date:27 November 2025
  • Workload:100%
  • Contract type:Permanent position
  • Place of work:Basel

Job summary

Join Abbott as a Quality Assurance Manager in Basel, leading TPM! Enjoy a dynamic work environment with growth opportunities.

Tasks

  • Ensure TPMs meet cGMP and Abbott's safety and quality standards.
  • Develop Quality Improvement Plans and drive continuous improvement efforts.
  • Lead QA activities during product technology transfers and audits.

Skills

  • Degree in Pharmacy, Biotechnology, or related field with 10+ years experience.
  • Strong knowledge of GMP and international quality standards.
  • Proven leadership skills and excellent English communication ability.

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<p><b>Quality Assurance Manager – Third Party Manufacturing & Technical Transfer (EMEA)</b></p><p></p><p><b>About Abbott</b></p><p></p><p><b>Abbott</b> is a global healthcare leader, creating breakthrough science to improve people’s health. We anticipate changes in medical science and technology to stay ahead and make a difference.</p><p></p><p><b>The Opportunity</b></p><p></p><p>We are looking for a <b>Quality Assurance Manager</b> to manage Third Party Manufacturing (TPM) and lead Product Technology Transfers across EMEA. This role is based at our Basel site within the Established Pharmaceutical Division, where we deliver trusted medicines to fast-growing markets worldwide.</p><p></p><p><b>What You’ll Do</b></p><ul><li><p>Ensure TPMs meet cGMP, Abbott’s and regulatory standards for safe, high-quality products.</p></li><li><p>Develop and implement Quality Improvement Plans and drive continuous improvement.</p></li><li><p>Monitor quality performance and manage Quality Technical Agreements.</p></li><li><p>Act as QA lead for deviations and complaints investigations, CAPA, , product release issues, validation and change controls.</p></li><li><p>Coordinate audits, new projects, and compliance initiatives with TPMs and internal teams.</p></li><li><p>Lead QA activities during technology transfers, including change control, method validation, and process verification.</p></li><li><p>Support new product introductions, geographic expansion, and portfolio growth.</p></li><li><p>Collaborate across functions and regions to resolve technical issues and maintain compliance.</p></li></ul><p></p><p><b>What We’re Looking For</b></p><ul><li><p>Degree in Pharmacy, Pharmaceutical Technology, Biotechnology, or related field.</p></li><li><p>10+ years of experience in pharmaceutical manufacturing (Quality, Production, Technical Support).</p></li><li><p>Strong knowledge of GMP and international quality standards.</p></li><li><p>Excellent communication skills in English; French is a plus.</p></li><li><p>Proven leadership and ability to foster collaboration.</p></li><li><p>Willingness to travel up to 30%.</p></li></ul><p></p><p><b>Preferred Skills</b></p><ul><li><p>Expertise in cGMP for solid, liquid, injectable, and biosimilar products.</p></li><li><p>Certifications such as IRCA Lead Auditor or GMP-GDP training are an advantage.</p></li></ul><p></p><p><b>Why Abbott?</b></p><p></p><p>At Abbott, you’ll work on projects that matter and have opportunities to grow your career. We offer flexibility, development programs, and a supportive environment where your expertise makes a global impact.</p><p></p><p><b>Apply Now</b><br />Shape the future of healthcare with Abbott.</p><p></p><p></p>

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