CO
Quality Assurance Manager – Third Party Manufacturing & Technical Transfer (EMEA)
Confidentiel
Part-time
Description du poste
About Abbott
Abbott
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.
Quality Assurance Manager – Third Party Manufacturing & Technical Transfer (EMEA)
The Opportunity
We 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
•
Ensure TPMs meet cGMP, Abbott’s and regulatory standards for safe, high-quality products.
•
Develop and implement Quality Improvement Plans and drive continuous improvement.
•
Monitor quality performance and manage Quality Technical Agreements.
•
Act as QA lead for deviations and complaints investigations, CAPA, , product release issues, validation and change controls.
•
Coordinate audits, new projects, and compliance initiatives with TPMs and internal teams.
•
Lead QA activities during technology transfers, including change control, method validation, and process verification.
•
Support new product introductions, geographic expansion, and portfolio growth.
•
Collaborate across functions and regions to resolve technical issues and maintain compliance.
What We’re Looking For
•
Degree in Pharmacy, Pharmaceutical Technology, Biotechnology, or related field.
•
10+ years of experience in pharmaceutical manufacturing (Quality, Production, Technical Support).
•
Strong knowledge of GMP and international quality standards.
•
Excellent communication skills in English; French is a plus.
•
Proven leadership and ability to foster collaboration.
•
Willingness to travel up to 30%.
Preferred Skills
•
Expertise in cGMP for solid, liquid, injectable, and biosimilar products.
•
Certifications such as IRCA Lead Auditor or GMP-GDP training are an advantage.
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.
Connect with us at
www.abbott.com (http://www.abbott.com/)
, on LinkedIn at
www.linkedin.com/company/abbott-/ (http://www.linkedin.com/company/abbott-/)
, on Facebook at
www.facebook.com/Abbott (http://www.facebook.com/Abbott)
and on Twitter @AbbottNews and @AbbottGlobal.
Abbott
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.
Quality Assurance Manager – Third Party Manufacturing & Technical Transfer (EMEA)
The Opportunity
We 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
•
Ensure TPMs meet cGMP, Abbott’s and regulatory standards for safe, high-quality products.
•
Develop and implement Quality Improvement Plans and drive continuous improvement.
•
Monitor quality performance and manage Quality Technical Agreements.
•
Act as QA lead for deviations and complaints investigations, CAPA, , product release issues, validation and change controls.
•
Coordinate audits, new projects, and compliance initiatives with TPMs and internal teams.
•
Lead QA activities during technology transfers, including change control, method validation, and process verification.
•
Support new product introductions, geographic expansion, and portfolio growth.
•
Collaborate across functions and regions to resolve technical issues and maintain compliance.
What We’re Looking For
•
Degree in Pharmacy, Pharmaceutical Technology, Biotechnology, or related field.
•
10+ years of experience in pharmaceutical manufacturing (Quality, Production, Technical Support).
•
Strong knowledge of GMP and international quality standards.
•
Excellent communication skills in English; French is a plus.
•
Proven leadership and ability to foster collaboration.
•
Willingness to travel up to 30%.
Preferred Skills
•
Expertise in cGMP for solid, liquid, injectable, and biosimilar products.
•
Certifications such as IRCA Lead Auditor or GMP-GDP training are an advantage.
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.
Connect with us at
www.abbott.com (http://www.abbott.com/)
, on LinkedIn at
www.linkedin.com/company/abbott-/ (http://www.linkedin.com/company/abbott-/)
, on Facebook at
www.facebook.com/Abbott (http://www.facebook.com/Abbott)
and on Twitter @AbbottNews and @AbbottGlobal.
Informations détaillées
Type de contrat
Part-time
Localisation
Allschwil
Secteur d'activité
Chimie / Pharma
Pays
Switzerland
CVthèque Suisse
Soyez visible par les meilleurs recruteurs suisses et accédez à des opportunités exclusives adaptées à votre profil professionnel.
Visibilité maximale
100% sécurisé
Opportunités exclusives

En ligne
Léa Harfi
Experte RH Suisse
🔥
Service Personnalisé
CV Professionnel Suisse
Optimisé ATS • Format suisse authentique • Livraison 24-72h garantie
Rédaction complète
2 Lettres incluses
Livraison rapide
Garantie satisfaction
39€
Je veux mon CV professionnel
Prix unique, tout inclus