Abbott
Quality Assurance Manager – Third Party Manufacturing & Technical Transfer(m/w/x)
Full-timeOn-siteSenior
Basel, Allschwil
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Leading sterile GMP drug product manufacturing transfers from clinical to commercial stages. Aseptic manufacturing know-how for protein drug products, including lyophilization, required. Agile career path, compensation programs recognizing high performance.
Requirements
- Ph.D. or Master in pharmaceutical sciences, engineering, chemistry, or biochemistry
- Significant biotech/pharma industry experience
- Knowledge of drug product technical transfer issues
- Know-how in aseptic product manufacture for protein drug products including lyophilization
- Knowledge of ADCs/highly potent drug product manufacturing highly desirable
- Good leadership and interpersonal skills
- Proven ability as team player
- Ability to manage cross-functional teams
- Very good planning and organizing skills
- Project management skills
- Risk management skills
- Excellent communication skills
- Command of English both written and oral
Tasks
- Ensure activities meet quality, regulatory, and safety standards
- Lead technical transfer for sterile GMP drug product manufacturing
- Manage drug product transfers from clinical to commercial stages
- Define project scope, timelines, risks, and milestones
- Track project progress effectively
- Lead process setup, scale-up, and implementation at GMP sites
- Prepare and maintain technical transfer documentation
- Drive GMP change management
- Handle deviations and CAPAs
- Support regulatory documentation, inspections, audits, and customer interactions
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Compensation programs recognizing high performance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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- Lonza
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Leading sterile GMP drug product manufacturing transfers from clinical to commercial stages. Aseptic manufacturing know-how for protein drug products, including lyophilization, required. Agile career path, compensation programs recognizing high performance.
Requirements
- Ph.D. or Master in pharmaceutical sciences, engineering, chemistry, or biochemistry
- Significant biotech/pharma industry experience
- Knowledge of drug product technical transfer issues
- Know-how in aseptic product manufacture for protein drug products including lyophilization
- Knowledge of ADCs/highly potent drug product manufacturing highly desirable
- Good leadership and interpersonal skills
- Proven ability as team player
- Ability to manage cross-functional teams
- Very good planning and organizing skills
- Project management skills
- Risk management skills
- Excellent communication skills
- Command of English both written and oral
Tasks
- Ensure activities meet quality, regulatory, and safety standards
- Lead technical transfer for sterile GMP drug product manufacturing
- Manage drug product transfers from clinical to commercial stages
- Define project scope, timelines, risks, and milestones
- Track project progress effectively
- Lead process setup, scale-up, and implementation at GMP sites
- Prepare and maintain technical transfer documentation
- Drive GMP change management
- Handle deviations and CAPAs
- Support regulatory documentation, inspections, audits, and customer interactions
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Compensation programs recognizing high performance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Lonza
Industry
Pharmaceuticals
Description
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
Not a perfect match?
- Abbott
Quality Assurance Manager – Third Party Manufacturing & Technical Transfer(m/w/x)
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Full-timeOn-siteSeniorBasel - F. Hoffmann-La Roche AG
Drug Product Technology Strategy Project Leader(m/w/x)
Full-timeOn-siteSeniorBasel - Roche
Validation Expert(m/w/x)
Full-timeOn-siteExperiencedKaiseraugst - 1201 F. Hoffmann-La Roche AG
Site Transfer and User Team Lead - MSAT KAU(m/w/x)
Full-timeOn-siteSeniorKaiseraugst