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Global Quality GVP Manager(m/w/x)
Description
In this role, you will oversee quality assurance in global pharmacovigilance, guiding initiatives and collaborating with various stakeholders. Your day-to-day responsibilities will include developing audit strategies, performing audits, and ensuring compliance with quality standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •University degree in Life Sciences or related field
- •Minimum 5 years’ experience in the pharmaceutical industry with GVP responsibilities
- •Proven experience in audit management and/or quality assurance
- •Strong knowledge of EU/US/Rest of World GVP regulations
- •Experience with QA systems and auditing is highly valued
- •Structured, results-oriented professional
- •Strong interpersonal skills
- •Flexible, communicative approach
- •Proactive and resilient under pressure
- •Adept at multitasking
- •Passionate about making a positive impact for patients
Education
Work Experience
5 years
Tasks
- •Ensure quality oversight in global pharmacovigilance activities
- •Guide and support global and local pharmacovigilance initiatives
- •Contribute to the development of audit strategies and plans for GVP processes
- •Act as GVP Audit Program Owner when delegated
- •Support the Global GPV organization in PV QMS activities
- •Perform and coordinate internal and external PV audits
- •Collaborate with Medical Affairs, Regulatory Affairs, and Affiliates
- •Ensure qualification of global and local service providers in GVP
- •Represent quality assurance during inspections and audits
Languages
English – Business Fluent
Benefits
Family Support
- •Emphasis on work/life balance
Informal Culture
- •Collaborative and team-oriented environment
Career Advancement
- •Opportunities for professional growth
Other Benefits
- •Diversity and Inclusion
- •Competitive benefits package
Competitive Pay
- •Competitive compensation
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Global Quality GVP Manager(m/w/x)
The AI Job Search Engine
Description
In this role, you will oversee quality assurance in global pharmacovigilance, guiding initiatives and collaborating with various stakeholders. Your day-to-day responsibilities will include developing audit strategies, performing audits, and ensuring compliance with quality standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •University degree in Life Sciences or related field
- •Minimum 5 years’ experience in the pharmaceutical industry with GVP responsibilities
- •Proven experience in audit management and/or quality assurance
- •Strong knowledge of EU/US/Rest of World GVP regulations
- •Experience with QA systems and auditing is highly valued
- •Structured, results-oriented professional
- •Strong interpersonal skills
- •Flexible, communicative approach
- •Proactive and resilient under pressure
- •Adept at multitasking
- •Passionate about making a positive impact for patients
Education
Work Experience
5 years
Tasks
- •Ensure quality oversight in global pharmacovigilance activities
- •Guide and support global and local pharmacovigilance initiatives
- •Contribute to the development of audit strategies and plans for GVP processes
- •Act as GVP Audit Program Owner when delegated
- •Support the Global GPV organization in PV QMS activities
- •Perform and coordinate internal and external PV audits
- •Collaborate with Medical Affairs, Regulatory Affairs, and Affiliates
- •Ensure qualification of global and local service providers in GVP
- •Represent quality assurance during inspections and audits
Languages
English – Business Fluent
Benefits
Family Support
- •Emphasis on work/life balance
Informal Culture
- •Collaborative and team-oriented environment
Career Advancement
- •Opportunities for professional growth
Other Benefits
- •Diversity and Inclusion
- •Competitive benefits package
Competitive Pay
- •Competitive compensation
About the Company
Sobi
Industry
Pharmaceuticals
Description
The company is a specialized biopharmaceutical company dedicated to rare diseases and committed to developing innovative therapies.
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Manager Quality Control Pharma(m/w/x)
Full-timeOn-siteSeniorWeil am Rhein, Rheinfelden (Baden) - 1201 F. Hoffmann-La Roche AG
QA Manager(m/w/x)
Full-timeOn-siteSeniorKaiseraugst