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15928en
- Contract
- English
- Mid-Senior level
- Research & Development
- Switzerland
- Healthcare & Life Sciences
Skills
Production Campaigns, Risk analysis, Campaign reports, GMP, cGMP
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This vacancy has now expired
On behalf of our client, a multinational manufacturing company for the pharmaceutical, biotechnology and nutrition sectors we are looking for a Bio Process Engineer.
Start Date: As soon as possible
Location: Visp
Workload: 100%
Duration: 9 months (with possible extension)
Description:
In this role, you will oversee production campaigns within the BioConjugates IBEX facilities, focusing on the synthesis of bioconjugates. Your role involves conducting risk analyses, ensuring compliance with GMP, safety, and cleaning regulations, and representing production in direct customer interactions. You will collaborate with interdisciplinary teams on projects including investments and process optimization.
Your mission:
- Ensure timely, high-quality, and cost-optimized production in compliance with safety, quality, and environmental regulations.
- Independently execute operational batch record reviews and contribute to risk analyses and subsequent measures.
- Conduct production campaigns according to cGMP guidelines, troubleshooting problems and proposing solutions as needed.
- Document processes, prepare campaign reports, and participate in product reviews.
- Identify and implement improvement opportunities in collaboration with project teams.
- Ensure implementation of relevant GMP documents and train employees on assigned products.
Your background:
- Fluency in German and English OR English only.
- Minimum 2 years of relevant experience.
What’s on Offer:
Join a dynamic team in a leading global pharmaceutical company, contributing to the advancement of bioconjugate production and pharmaceutical innovation.
Start Date: As soon as possible
Location: Visp
Workload: 100%
Duration: 9 months (with possible extension)
Description:
In this role, you will oversee production campaigns within the BioConjugates IBEX facilities, focusing on the synthesis of bioconjugates. Your role involves conducting risk analyses, ensuring compliance with GMP, safety, and cleaning regulations, and representing production in direct customer interactions. You will collaborate with interdisciplinary teams on projects including investments and process optimization.
Your mission:
- Ensure timely, high-quality, and cost-optimized production in compliance with safety, quality, and environmental regulations.
- Independently execute operational batch record reviews and contribute to risk analyses and subsequent measures.
- Conduct production campaigns according to cGMP guidelines, troubleshooting problems and proposing solutions as needed.
- Document processes, prepare campaign reports, and participate in product reviews.
- Identify and implement improvement opportunities in collaboration with project teams.
- Ensure implementation of relevant GMP documents and train employees on assigned products.
Your background:
- Fluency in German and English OR English only.
- Minimum 2 years of relevant experience.
What’s on Offer:
Join a dynamic team in a leading global pharmaceutical company, contributing to the advancement of bioconjugate production and pharmaceutical innovation.
I manage this role