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Global Head QA Operations Aseptics(m/w/x)
Coordinating global Quality Units for sterile biopharmaceutical production. 15 years biopharmaceutical manufacturing QA experience required. Global coordination across multiple production sites.
Requirements
- Graduate in Chemistry, Pharmacy, Microbiology, Biotechnology, or related science
- 15 years experience in biopharmaceuticals manufacturing and Quality Assurance
- Operational knowledge of aseptic processing and medical device quality requirements
- Excellent GMP knowledge and aseptic environments
- QA/QC knowledge and solid experience with Authorities' inspections
- Fluent English (written and spoken)
Tasks
- Coordinate and support Quality Units
- Implement and develop Quality systems and programs
- Monitor Quality system performance
- Evaluate Quality performance using KPIs and reporting
- Report progress and issues to QA management
- Ensure timely follow-up on action plans
- Prepare, execute, and follow up on health authority inspections
- Determine trends for quality improvement
- Identify opportunities for quality improvement
- Support TpT and OTBA initiatives
- Act as NOSCEE SPOC
- Ensure alignment with global standards
- Guide organizational improvement and development
- Drive Operational Excellence
- Improve financial outcomes
- Drive harmonization initiatives across sites
- Drive process improvement initiatives across sites
- Act as Supply QA contact
- Support Annex 16 clarifications
- Manage artwork problems
- Implement follow-up measures for artwork problems
- Coordinate and support supplier certification programs
- Perform site compliance checks
- Support the site escalation process
- Support quality escalation processes
- Ensure timely communication of critical quality events
- Ensure robust resolution of critical quality events
Work Experience
- 15 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- aseptic processing
- GMP
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Global Head QA Operations Aseptics(m/w/x)
Coordinating global Quality Units for sterile biopharmaceutical production. 15 years biopharmaceutical manufacturing QA experience required. Global coordination across multiple production sites.
Requirements
- Graduate in Chemistry, Pharmacy, Microbiology, Biotechnology, or related science
- 15 years experience in biopharmaceuticals manufacturing and Quality Assurance
- Operational knowledge of aseptic processing and medical device quality requirements
- Excellent GMP knowledge and aseptic environments
- QA/QC knowledge and solid experience with Authorities' inspections
- Fluent English (written and spoken)
Tasks
- Coordinate and support Quality Units
- Implement and develop Quality systems and programs
- Monitor Quality system performance
- Evaluate Quality performance using KPIs and reporting
- Report progress and issues to QA management
- Ensure timely follow-up on action plans
- Prepare, execute, and follow up on health authority inspections
- Determine trends for quality improvement
- Identify opportunities for quality improvement
- Support TpT and OTBA initiatives
- Act as NOSCEE SPOC
- Ensure alignment with global standards
- Guide organizational improvement and development
- Drive Operational Excellence
- Improve financial outcomes
- Drive harmonization initiatives across sites
- Drive process improvement initiatives across sites
- Act as Supply QA contact
- Support Annex 16 clarifications
- Manage artwork problems
- Implement follow-up measures for artwork problems
- Coordinate and support supplier certification programs
- Perform site compliance checks
- Support the site escalation process
- Support quality escalation processes
- Ensure timely communication of critical quality events
- Ensure robust resolution of critical quality events
Work Experience
- 15 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- aseptic processing
- GMP
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Novartis Pharmaceutical Manufacturing GmbH
Industry
Pharmaceuticals
Description
The company aims to reimagine medicine to improve and extend people’s lives.
Not a perfect match?
- Novartis Pharmaceutical Manufacturing GmbH
Global Head QA Operations Aseptics(m/w/x)
Full-timeOn-siteSeniorSchaftenau - Novartis Pharmaceutical Manufacturing GmbH
Quality Manager Pilot Plant(m/w/x)
Full-timeOn-siteManagementSchaftenaufrom 65,605.54 / year - Novartis Pharmaceutical Manufacturing GmbH
Quality Team Leader QC(m/w/x)
Full-timeOn-siteSeniorSchaftenaufrom 78,383.9 / year - Novartis Pharmaceutical Manufacturing GmbH
Process Expert(m/w/x)
Full-timeOn-siteExperiencedSchaftenaufrom 59,781.96 / year - Novartis Pharmaceutical Manufacturing GmbH
Senior Expert Science & Technology (Process Analytical Sciences)(m/w/x)
Full-timeOn-siteManagementSchaftenaufrom 65,605.54 / year