Third Party Manufacturer and Technical Transfer QA Manager- EMEA

27 November 2025
100%
Permanent position
Basel

Job summary

Join Abbott as a Quality Assurance Manager in Basel, EMEA.

Tasks

Manage Third Party Manufacturing and ensure cGMP compliance.
Lead technical transfers and implement Quality Improvement Plans.
Support new product launches and monitor quality performance.

Skills

Requires a degree in Pharmacy or related field and 10+ years experience.
Strong knowledge of GMP and international quality standards.
Excellent communication skills; French is a plus.

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About the job

Quality Assurance Manager – Third Party Manufacturing & Technical Transfer (EMEA)About AbbottAbbott 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.The OpportunityWe are looking for a Quality Assurance Manager 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.What You’ll Do<ul><li>Ensure TPMs meet cGMP, Abbott’s and regulatory standards for safe, high-quality products.</li><li>Develop and implement Quality Improvement Plans and drive continuous improvement.</li><li>Monitor quality performance and manage Quality Technical Agreements.</li><li>Act as QA lead for deviations and complaints investigations, CAPA, , product release issues, validation and change controls.</li><li>Coordinate audits, new projects, and compliance initiatives with TPMs and internal teams.</li><li>Lead QA activities during technology transfers, including change control, method validation, and process verification.</li><li>Support new product introductions, geographic expansion, and portfolio growth.</li><li>Collaborate across functions and regions to resolve technical issues and maintain compliance.</li></ul>What We’re Looking For<ul><li>Degree in Pharmacy, Pharmaceutical Technology, Biotechnology, or related field.</li><li>10+ years of experience in pharmaceutical manufacturing (Quality, Production, Technical Support).</li><li>Strong knowledge of GMP and international quality standards.</li><li>Excellent communication skills in English; French is a plus.</li><li>Proven leadership and ability to foster collaboration.</li><li>Willingness to travel up to 30%.</li></ul>Preferred Skills<ul><li>Expertise in cGMP for solid, liquid, injectable, and biosimilar products.</li><li>Certifications such as IRCA Lead Auditor or GMP-GDP training are an advantage.</li></ul>Why Abbott?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.Apply Now Shape the future of healthcare with Abbott.