Jobs

Third Party Manufacturer and Technical Transfer QA Manager- EMEA
Switzerland - Basel
·
On-site
·
Full-time
·
1w ago
Benefits & Perks
•Flexibility
•Development programs
Required Skills
GMP knowledge
Quality Assurance
Leadership
English
Regulatory compliance
JOB DESCRIPTION:
Quality Assurance Manager – Third Party Manufacturing & Technical Transfer (EMEA)
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.
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.
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Monitor quality performance and manage Quality Technical Agreements.
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Act as QA lead for deviations and complaints investigations, CAPA, , product release issues, validation and change controls.
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Coordinate audits, new projects, and compliance initiatives with TPMs and internal teams.
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Lead QA activities during technology transfers, including change control, method validation, and process verification.
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Support new product introductions, geographic expansion, and portfolio growth.
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Collaborate across functions and regions to resolve technical issues and maintain compliance.
What We’re Looking For
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Degree in Pharmacy, Pharmaceutical Technology, Biotechnology, or related field.
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10+ years of experience in pharmaceutical manufacturing (Quality, Production, Technical Support).
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Strong knowledge of GMP and international quality standards.
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Excellent communication skills in English; French is a plus.
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Proven leadership and ability to foster collaboration.
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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.
The base pay for this position is
N/A
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Operations Quality
DIVISION:
EPD Established Pharma:
LOCATION:
Switzerland > Allschwil : H-127
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 25 % of the Time
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Not Applicable
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About Abbott

Abbott
PublicAbbott is a global healthcare company that develops medical devices, diagnostics, branded generic medicines, and nutrition products.
10,001+
Employees
Abbott Park
Headquarters
Reviews
3.4
10 reviews
Work Life Balance
2.5
Compensation
4.0
Culture
2.8
Career
3.2
Management
2.5
45%
Recommend to a Friend
Pros
Good benefits and compensation
Supportive management/teams
Good company reputation and mission
Cons
Poor management and communication
Stressful work environment
Limited career advancement/favoritism
Salary Ranges
1,330 data points
Mid/L4
Mid/L4 · Clinical Specialist
192 reports
$122,947
total / year
Base
$107,979
Stock
-
Bonus
$14,968
$82,590
$185,149
Interview Experience
3 interviews
Difficulty
2.7
/ 5
Duration
14-28 weeks
Offer Rate
67%
Experience
Positive 67%
Neutral 33%
Negative 0%
Interview Process
1
Application Review
2
Recruiter Screen
3
Phone Screen
4
Hiring Manager Interview
5
In-person/Final Interview
6
Offer
Common Questions
Technical Knowledge
Behavioral/STAR
Past Experience
Culture Fit
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