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Site Quality Head(m/w/x)
Description
As the Site Quality Head, you will lead efforts to uphold world-class quality and compliance at a strategic manufacturing site, ensuring adherence to regulatory standards while fostering a culture of continuous improvement and collaboration.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •10–15 years of experience in the pharmaceutical or chemical industry
- •University degree in Chemistry, Pharmacy, or related discipline
- •Strong knowledge of regulatory requirements and cGMP standards
- •Experience with FDA/Swissmedic regulations and compliance
- •Dynamic, resilient, and versatile approach to problem-solving
- •Demonstrated people leadership and team management skills
- •Excellent communication skills and ability to collaborate across functions
- •Fluency in German and English
Education
Work Experience
10 - 15 years
Tasks
- •Lead the Site Quality organization
- •Foster a culture of compliance and continuous improvement
- •Ensure adherence to cGMP and regulatory requirements
- •Act as Qualified Person for site operations
- •Oversee quality governance across all GxP functions
- •Ensure robust risk management
- •Approve or reject raw materials, facilities, utilities, and finished products
- •Drive execution of training programs
- •Maintain compliance with DI and eCompliance standards
- •Manage internal and external audits and inspections
- •Handle regulatory submissions
- •Ensure effective complaint investigations
- •Manage exception processes
Languages
German – Business Fluent
English – Business Fluent
- Endress+HauserFull-timeWith HomeofficeSeniorReinach
- BASF Grenzach GmbH
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Site Quality Head(m/w/x)
The AI Job Search Engine
Description
As the Site Quality Head, you will lead efforts to uphold world-class quality and compliance at a strategic manufacturing site, ensuring adherence to regulatory standards while fostering a culture of continuous improvement and collaboration.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •10–15 years of experience in the pharmaceutical or chemical industry
- •University degree in Chemistry, Pharmacy, or related discipline
- •Strong knowledge of regulatory requirements and cGMP standards
- •Experience with FDA/Swissmedic regulations and compliance
- •Dynamic, resilient, and versatile approach to problem-solving
- •Demonstrated people leadership and team management skills
- •Excellent communication skills and ability to collaborate across functions
- •Fluency in German and English
Education
Work Experience
10 - 15 years
Tasks
- •Lead the Site Quality organization
- •Foster a culture of compliance and continuous improvement
- •Ensure adherence to cGMP and regulatory requirements
- •Act as Qualified Person for site operations
- •Oversee quality governance across all GxP functions
- •Ensure robust risk management
- •Approve or reject raw materials, facilities, utilities, and finished products
- •Drive execution of training programs
- •Maintain compliance with DI and eCompliance standards
- •Manage internal and external audits and inspections
- •Handle regulatory submissions
- •Ensure effective complaint investigations
- •Manage exception processes
Languages
German – Business Fluent
English – Business Fluent
About the Company
Novartis
Industry
Pharmaceuticals
Description
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
- Endress+Hauser
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