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Quality Assurance Manager – Third Party Manufacturing & Technical Transfer(m/w/x)
Description
As a Quality Assurance Manager, you will ensure that third-party manufacturers meet high standards for quality and safety. This role involves developing improvement plans, leading audits, and supporting new product launches while collaborating with various teams to maintain compliance.
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Requirements
- •Degree in Pharmacy, Pharmaceutical Technology, Biotechnology, or related field
- •10+ years of experience in pharmaceutical manufacturing
- •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%
- •Expertise in cGMP for solid, liquid, injectable, and biosimilar products
- •Certifications such as IRCA Lead Auditor or GMP-GDP training are an advantage
Education
Work Experience
10 years
Tasks
- •Ensure TPMs meet cGMP and regulatory standards
- •Develop and implement Quality Improvement Plans
- •Drive continuous improvement initiatives
- •Monitor quality performance and manage Quality Technical Agreements
- •Act as QA lead for deviations and complaints investigations
- •Oversee CAPA and product release issues
- •Manage validation and change controls
- •Coordinate audits and compliance initiatives with TPMs
- •Lead QA activities during technology transfers
- •Support new product introductions and geographic expansion
- •Collaborate across functions to resolve technical issues
Languages
English – Business Fluent
French – Basic
Benefits
Flexible Working
- •Flexibility
Learning & Development
- •Development programs
Other Benefits
- •Supportive environment
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Quality Assurance Manager – Third Party Manufacturing & Technical Transfer(m/w/x)
The AI Job Search Engine
Description
As a Quality Assurance Manager, you will ensure that third-party manufacturers meet high standards for quality and safety. This role involves developing improvement plans, leading audits, and supporting new product launches while collaborating with various teams to maintain compliance.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in Pharmacy, Pharmaceutical Technology, Biotechnology, or related field
- •10+ years of experience in pharmaceutical manufacturing
- •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%
- •Expertise in cGMP for solid, liquid, injectable, and biosimilar products
- •Certifications such as IRCA Lead Auditor or GMP-GDP training are an advantage
Education
Work Experience
10 years
Tasks
- •Ensure TPMs meet cGMP and regulatory standards
- •Develop and implement Quality Improvement Plans
- •Drive continuous improvement initiatives
- •Monitor quality performance and manage Quality Technical Agreements
- •Act as QA lead for deviations and complaints investigations
- •Oversee CAPA and product release issues
- •Manage validation and change controls
- •Coordinate audits and compliance initiatives with TPMs
- •Lead QA activities during technology transfers
- •Support new product introductions and geographic expansion
- •Collaborate across functions to resolve technical issues
Languages
English – Business Fluent
French – Basic
Benefits
Flexible Working
- •Flexibility
Learning & Development
- •Development programs
Other Benefits
- •Supportive environment
About the Company
Abbott
Industry
Healthcare
Description
Das Unternehmen ist ein weltweit führendes Unternehmen im Gesundheitswesen, das bahnbrechende wissenschaftliche Erkenntnisse nutzt und Lösungen zur Verbesserung der Gesundheit der Menschen entwickelt.
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