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Leading technical transfers for aseptic fill-and-finish processes at global life sciences firm. Experience in aseptic/sterile drug manufacturing required. Agile career progression.
Requirements
- Experience in aseptic/sterile drug manufacturing
- Know-how in sterility assurance principles
- Equipment qualification and cleaning validation
- Degree in Biotechnology, Pharmacy, or equivalent
- Strong communication and technical translation
- Proactive problem-solving and responsibility
- Cross-functional leadership and decision-making
- Proficiency in English
- German language skills (plus)
Tasks
- Lead technical transfers for aseptic fill-and-finish processes
- Evaluate and develop fit-for-purpose manufacturing processes
- Manage information transfer and process-related risks
- Oversee change control using structured tools
- Resolve technical challenges as the primary process owner
- Drive process monitoring and control strategies
- Perform complex data analyses on manufacturing processes
- Lead cross-functional projects to expand facility capabilities
- Qualify equipment, filling lines, and facilities
- Provide PPQ support for BLA projects
- Manage complex deviations and customer complaints
- Identify root causes using scientific and statistical insights
- Ensure inspection readiness for internal and external audits
- Support front and back-office audit activities
- Represent the area during facility tours
- Coach and mentor colleagues in project leadership
- Drive concept implementation across the site and network
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GMP
- Aseptic processing
- Sterility assurance
- Cleaning validation
- Room qualification
Benefits
Bonuses & Incentives
- Performance-based compensation programs
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
Not a perfect match?
- CH12 Lonza AGFull-timeOn-siteSeniorStein (AR)
- Lonza
Process Expert - prefilled Syringes(m/w/x)
Full-timeOn-siteExperiencedStein (AR) - CH12 Lonza AG
Process Expert - sterile filling of biopharmaceutical Drug Product(m/w/x)
Full-timeOn-siteExperiencedStein (AR) - Lonza
Process Expert - Lyophilized Vials(m/w/x)
Full-timeOn-siteExperiencedStein (AR) - CH12 Lonza AG
Global MSAT Drug Product Qualification and Validation Lead(m/w/x)
Full-timeOn-siteSeniorStein (AR)
Leading technical transfers for aseptic fill-and-finish processes at global life sciences firm. Experience in aseptic/sterile drug manufacturing required. Agile career progression.
Requirements
- Experience in aseptic/sterile drug manufacturing
- Know-how in sterility assurance principles
- Equipment qualification and cleaning validation
- Degree in Biotechnology, Pharmacy, or equivalent
- Strong communication and technical translation
- Proactive problem-solving and responsibility
- Cross-functional leadership and decision-making
- Proficiency in English
- German language skills (plus)
Tasks
- Lead technical transfers for aseptic fill-and-finish processes
- Evaluate and develop fit-for-purpose manufacturing processes
- Manage information transfer and process-related risks
- Oversee change control using structured tools
- Resolve technical challenges as the primary process owner
- Drive process monitoring and control strategies
- Perform complex data analyses on manufacturing processes
- Lead cross-functional projects to expand facility capabilities
- Qualify equipment, filling lines, and facilities
- Provide PPQ support for BLA projects
- Manage complex deviations and customer complaints
- Identify root causes using scientific and statistical insights
- Ensure inspection readiness for internal and external audits
- Support front and back-office audit activities
- Represent the area during facility tours
- Coach and mentor colleagues in project leadership
- Drive concept implementation across the site and network
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GMP
- Aseptic processing
- Sterility assurance
- Cleaning validation
- Room qualification
Benefits
Bonuses & Incentives
- Performance-based compensation programs
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
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?
- CH12 Lonza AG
Head MSAT, Drug Product Stein(m/w/x)
Full-timeOn-siteSeniorStein (AR) - Lonza
Process Expert - prefilled Syringes(m/w/x)
Full-timeOn-siteExperiencedStein (AR) - CH12 Lonza AG
Process Expert - sterile filling of biopharmaceutical Drug Product(m/w/x)
Full-timeOn-siteExperiencedStein (AR) - Lonza
Process Expert - Lyophilized Vials(m/w/x)
Full-timeOn-siteExperiencedStein (AR) - CH12 Lonza AG
Global MSAT Drug Product Qualification and Validation Lead(m/w/x)
Full-timeOn-siteSeniorStein (AR)