For our client, an international pharma company in Visp, we are looking for a Senior Bioprocess Engineer with significant work experience in Microbial, BioConjugates or Mammalian and a passion to engage in bringing improvement initiatives to life including engaging and driving operational readiness of roll-outs.General Information: Start date: ASAPEnd date: until 03/08/2026Contract: temporary via RandstadExtension: to be discussedWorkplace: VispWorkload:
For our client, an international pharma company in Visp, we are looking for a Senior Bioprocess Engineer with significant work experience in Microbial, BioConjugates or Mammalian and a passion to engage in bringing improvement initiatives to life including engaging and driving operational readiness of roll-outs.General Information: Start date: ASAPEnd date: until 03/08/2026Contract: temporary via RandstadExtension: to be discussedWorkplace: VispWorkload:
For our client, an international pharma company in Visp, we are looking for a Bioprocess Engineer DSP I.
General Information:
Start date: ASAP
End date: until 26/01/2026
Contract: temporary via Randstad
Extension: to be discussed
Workplace: Visp
Workload: 100%
Home office: not possible
...
Responsibilities:
Oversee, plan and support execution of manufacturing campaigns in the area of microbial fermentation.
Responsible to prepare and execute SHE, EM, operation and cleaning risk analysis for the assigned products and the implementation and control of defined measures.
Responsible to establish timely and with high quality the required production documentation (preparation and review of electronic batch records) specific to the assigned production area.
Perform manufacturing activities according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution.
Reviews production documentation and works on deviations, change requests and implementation of CAPAs to ensure high-quality GMP standards.
Working as production expert in Capital investment projects for building and commissioning of the manufacturing units. Responsible for delivering all input required for the specific set-up, commissioning and qualification of the manufacturing suites and equipment including automation.
Prepare, change and review DeltaV recipes for equipment and facility parts.
Coordinate and support Engineering and workshops for campaign preparation and change-over activities in the facility.
Execute innovation and improvement projects comprising general manufacturing aspects for the production plant.
Responsible for training of the operators for the manufacturing of the assigned products.
Represent own area / unit during customer audits and visits.
Perform other duties as assigned.
Your Profile:
Educational background in a scientific or technical field (preferred area: Biotechnology, Biochemistry or related disciplines)
1-3 years of professional experience with a MSc degree, or 3-5 years with a BSc degree
Good biotechnology expertise and/or knowledge in biotechnical engineering, preferably in the area of microbial fermentation
Fluent in English
Excellent GMP understanding
Good communication skills and interaction with all kinds of interfaces within the organization; strong team orientation
Structured, focused and well-organized working attitude
Open-minded for new ideas and suggestions
High motivation and dynamic drive
Solution-oriented
Nice to have:
MES and DeltaV system knowledge
German proficiency
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For our client, an international pharma company in Visp, we are looking for a Bioprocess Engineer DSP I.
General Information:
Start date: ASAP
End date: until 26/01/2026
Contract: temporary via Randstad
Extension: to be discussed
Workplace: Visp
Workload: 100%
Home office: not possible
...
Responsibilities:
Oversee, plan and support execution of manufacturing campaigns in the area of microbial fermentation.
Responsible to prepare and execute SHE, EM, operation and cleaning risk analysis for the assigned products and the implementation and control of defined measures.
Responsible to establish timely and with high quality the required production documentation (preparation and review of electronic batch records) specific to the assigned production area.
Perform manufacturing activities according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution.
Reviews production documentation and works on deviations, change requests and implementation of CAPAs to ensure high-quality GMP standards.
Working as production expert in Capital investment projects for building and commissioning of the manufacturing units. Responsible for delivering all input required for the specific set-up, commissioning and qualification of the manufacturing suites and equipment including automation.
Prepare, change and review DeltaV recipes for equipment and facility parts.
Coordinate and support Engineering and workshops for campaign preparation and change-over activities in the facility.
Execute innovation and improvement projects comprising general manufacturing aspects for the production plant.
Responsible for training of the operators for the manufacturing of the assigned products.
Represent own area / unit during customer audits and visits.
Perform other duties as assigned.
Your Profile:
Educational background in a scientific or technical field (preferred area: Biotechnology, Biochemistry or related disciplines)
1-3 years of professional experience with a MSc degree, or 3-5 years with a BSc degree
Good biotechnology expertise and/or knowledge in biotechnical engineering, preferably in the area of microbial fermentation
Fluent in English
Excellent GMP understanding
Good communication skills and interaction with all kinds of interfaces within the organization; strong team orientation
Structured, focused and well-organized working attitude