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Bioprocess Engineer USP/DSP( Microbial)/BioConjugates(m/w/x)
Executing clinical/commercial manufacturing operations and new facility qualification in biopharmaceutical production. Master's degree in life science or Bachelor's with pharma production experience required. Relocation assistance.
Requirements
- Master's degree or equivalent in Biotechnology, Biochemical Engineering, Biochemistry, Process Engineering, or related Life Science, or Bachelor's with pharmaceutical production experience
- Expertise in Upstream, Downstream processing, or Bio-conjugation technology
- Experience in bio-manufacturing and/or biopharmaceutical facility scaling up, with advantageous cGMP experience
- Excellent English communication skills
- German proficiency (plus)
- Organized and goal-oriented approach
- Willingness to consider new ideas
- Strong motivation
- Problem-solving approach
Tasks
- Execute timely operational activities for clinical and commercial manufacturing
- Maintain safety and quality standards
- Apply subject matter expertise to new facility design
- Apply subject matter expertise to new facility commissioning
- Apply subject matter expertise to new facility qualification
- Apply subject matter expertise to operational preparation
- Apply subject matter expertise to operational execution
- Apply subject matter expertise to operational cleaning
- Apply subject matter expertise to operational changeovers
- Lead upstream processing operations
- Lead downstream processing operations
- Lead Bio-Conjugates operations
- Perform cGMP-compliant manufacturing tasks
- Execute batch manufacturing
- Evaluate test results
- Troubleshoot equipment and recommend resolutions
- Review production documentation
- Address deviations
- Address change requests
- Implement CAPAs
- Assist with automation recipe development for equipment
- Assist with automation recipe development for facility components
- Assist with automation recipe review for equipment
- Assist with automation recipe review for facility components
- Train production personnel on assigned products
- Participate in audits
- Participate in customer visits
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Bonuses & Incentives
- Performance recognition programs
Career Advancement
- Agile career
Startup Environment
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
Not a perfect match?
- CH12 Lonza AGFull-timeOn-siteExperiencedVisp
- Lonza
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Bioprocess Engineer USP/DSP( Microbial)/BioConjugates(m/w/x)
Executing clinical/commercial manufacturing operations and new facility qualification in biopharmaceutical production. Master's degree in life science or Bachelor's with pharma production experience required. Relocation assistance.
Requirements
- Master's degree or equivalent in Biotechnology, Biochemical Engineering, Biochemistry, Process Engineering, or related Life Science, or Bachelor's with pharmaceutical production experience
- Expertise in Upstream, Downstream processing, or Bio-conjugation technology
- Experience in bio-manufacturing and/or biopharmaceutical facility scaling up, with advantageous cGMP experience
- Excellent English communication skills
- German proficiency (plus)
- Organized and goal-oriented approach
- Willingness to consider new ideas
- Strong motivation
- Problem-solving approach
Tasks
- Execute timely operational activities for clinical and commercial manufacturing
- Maintain safety and quality standards
- Apply subject matter expertise to new facility design
- Apply subject matter expertise to new facility commissioning
- Apply subject matter expertise to new facility qualification
- Apply subject matter expertise to operational preparation
- Apply subject matter expertise to operational execution
- Apply subject matter expertise to operational cleaning
- Apply subject matter expertise to operational changeovers
- Lead upstream processing operations
- Lead downstream processing operations
- Lead Bio-Conjugates operations
- Perform cGMP-compliant manufacturing tasks
- Execute batch manufacturing
- Evaluate test results
- Troubleshoot equipment and recommend resolutions
- Review production documentation
- Address deviations
- Address change requests
- Implement CAPAs
- Assist with automation recipe development for equipment
- Assist with automation recipe development for facility components
- Assist with automation recipe review for equipment
- Assist with automation recipe review for facility components
- Train production personnel on assigned products
- Participate in audits
- Participate in customer visits
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Bonuses & Incentives
- Performance recognition programs
Career Advancement
- Agile career
Startup Environment
- 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
Bioprocess Engineer in USP / DSP / BioConjugates(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Bioprocess Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Bioprocess Engineer BioConjugates(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Bioprocess Engineer Mammalian (USP/DSP)(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Bioprocess Engineer for MMM MC1 DSP(m/w/x)
Full-timeOn-siteExperiencedVisp