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Leading technical process transfers for aseptic fill-and-finish lines in pharmaceutical manufacturing, steering Industry 4.0 initiatives. Extensive hands-on experience in aseptic fill-and-finish operations and expert GMP qualification/validation knowledge required. Flexible working arrangements.
Requirements
- MSc or PhD in Pharmaceutical Technology, Chemical/Process Engineering, or relevant scientific discipline
- Experience managing direct reports and cultivating high-performance team culture
- Extensive hands-on experience in aseptic fill-and-finish operations
- Expert-level knowledge of qualification and validation frameworks within GMP environment
- Understanding of commercial manufacturing with advantageous clinical-scale production experience
- Fluency in English with advantageous German proficiency
Tasks
- Lead technical process transfers for aseptic fill-and-finish lines
- Ensure precision-led transitions from development to commercial manufacturing
- Identify and mitigate manufacturing risks
- Steer the site’s technical strategy and Industry 4.0 initiatives
- Represent the facility during regulatory inspections and client audits
- Maintain the MSAT department in a state of inspection readiness
- Oversee high-complexity technical investigations and root cause analyses
- Implement sustainable corrective and preventive actions
- Partner with Drug Product Operations and Development leadership
- Align site-level execution with corporate growth objectives
- Recruit and mentor a high-performing MSAT organization
- Foster a culture of innovation and psychological safety
Work Experience
- 7 - 10 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- aseptic fill-and-finish operations
- qualification and validation frameworks
- GMP environment
Benefits
Career Advancement
- Career development opportunity
Flexible Working
- Flexible working arrangements
Informal Culture
- Open culture
- Diverse workforce
Learning & Development
- Learning and self-developing culture
- Wide range of training
Retirement Plans
- Competitive pension fund plan
Bonuses & Incentives
- Annual bonus
Other Benefits
- Financial and non-financial benefits
Not a perfect match?
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
- Lonza
MSAT Expert Drug Product(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Process Validation Team Lead MSAT(m/w/x)
Full-timeOn-siteManagementVisp - Lonza
MSAT Process Expert Mammalian Upstream Large-Scale(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Process Expert MSAT Downstream- Mammalian Large Scale(m/w/x)
Full-timeOn-siteManagementVisp
Leading technical process transfers for aseptic fill-and-finish lines in pharmaceutical manufacturing, steering Industry 4.0 initiatives. Extensive hands-on experience in aseptic fill-and-finish operations and expert GMP qualification/validation knowledge required. Flexible working arrangements.
Requirements
- MSc or PhD in Pharmaceutical Technology, Chemical/Process Engineering, or relevant scientific discipline
- Experience managing direct reports and cultivating high-performance team culture
- Extensive hands-on experience in aseptic fill-and-finish operations
- Expert-level knowledge of qualification and validation frameworks within GMP environment
- Understanding of commercial manufacturing with advantageous clinical-scale production experience
- Fluency in English with advantageous German proficiency
Tasks
- Lead technical process transfers for aseptic fill-and-finish lines
- Ensure precision-led transitions from development to commercial manufacturing
- Identify and mitigate manufacturing risks
- Steer the site’s technical strategy and Industry 4.0 initiatives
- Represent the facility during regulatory inspections and client audits
- Maintain the MSAT department in a state of inspection readiness
- Oversee high-complexity technical investigations and root cause analyses
- Implement sustainable corrective and preventive actions
- Partner with Drug Product Operations and Development leadership
- Align site-level execution with corporate growth objectives
- Recruit and mentor a high-performing MSAT organization
- Foster a culture of innovation and psychological safety
Work Experience
- 7 - 10 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- aseptic fill-and-finish operations
- qualification and validation frameworks
- GMP environment
Benefits
Career Advancement
- Career development opportunity
Flexible Working
- Flexible working arrangements
Informal Culture
- Open culture
- Diverse workforce
Learning & Development
- Learning and self-developing culture
- Wide range of training
Retirement Plans
- Competitive pension fund plan
Bonuses & Incentives
- Annual bonus
Other Benefits
- Financial and non-financial benefits
About the Company
ten23 health
Industry
Pharmaceuticals
Description
The company is a human-centric strategic partner for the pharmaceutical industry and biotech start-ups, focusing on the development and testing of medicines.
Not a perfect match?
- CH12 Lonza AG
Head Manufacturing Science and Technology(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
MSAT Expert Drug Product(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Process Validation Team Lead MSAT(m/w/x)
Full-timeOn-siteManagementVisp - Lonza
MSAT Process Expert Mammalian Upstream Large-Scale(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Process Expert MSAT Downstream- Mammalian Large Scale(m/w/x)
Full-timeOn-siteManagementVisp