×
Register Here to Apply for Jobs or Post Jobs. X

Quality Assurance Manager – Third Party Manufacturing & Technical Transfer; EMEA

Job in 4123, Allschwil, Kanton Basel-Landschaft, Switzerland
Listing for: Abbott
Full Time position
Listed on 2025-12-10
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, QA Specialist / Manager, Quality Control / Manager, Data Analyst
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Quality Assurance Manager – Third Party Manufacturing & Technical Transfer (EMEA)

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.

#J-18808-Ljbffr
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary