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16262en
- Contract
- English, German
- Mid-Senior level
- Research & Development
- Switzerland
- Healthcare & Life Sciences
Skills
DeltaV, MES, automation, engineer, biotechnology, biopharmaceutical, pharmaceutical, DeltaV, Syncade, MES, Automatisierung, Ingenieur, Biotechnologie, Biopharmazie, Pharmazie,
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This vacancy has now expired
On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is looking for a Senior Bioprocess Engineer (MES/DeltaV). In this role, you primarily ensure the functionality of the automated production process in the process control system during cleaning and production and you take corrective action if there are any deviations.
Contract type - Contract
Start Date - October / November
Location - Visp, Canton Wallis
Workload - 100%
Duration - initially 10 months, likely to be internalised or extended.
Your mission:
• You create, test and optimize the automated production process. You are jointly responsible for automation right from the planning and engineering phase.
• You create recipes in DeltaV and monitor them during the run-in, qualification and production phases.
• You take part in risk and process deviation analyses.
• In collaboration with the plant team, you ensure documentation in accordance with cGMP.
• You continuously improve procedures and processes in compliance with safety, hygiene, environmental and quality requirements.
• Ability to identify risks related to safety or compliance/GMP and take measures to remedy them.
• Partial home office work is possible once you are established in the role.
Your background:
• Fluent German skills, with conversational English – team is German speaking, some colleagues are US-based.
• 3+ years of bioprocess recipe writing experience.
• Completed degree or training in the fields of biotechnology, chemistry, chemical engineering, biopharmaceutical sciences or a similar field.
• Very good understanding and experience in writing recipes in MES SYNC and/or DeltaV.
• Strong background in bioprocess engineering, or automation engineering with biopharma experience.
• Good understanding of IT process controls.
• Able to understand risk in GMP compliance when writing recipes.
• Strong team player and very good communication style.
• Ability to identify risks related to safety or compliance/GMP and take measures to remedy them.
What's on offer
• An initially 10 month contract, likely to be extended or internalised.
• A great opportunity to develop your career at a leading international biotechnology company.
• A competitive salary.
If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: hugo.palejowski@swisslinx.com.
Contract type - Contract
Start Date - October / November
Location - Visp, Canton Wallis
Workload - 100%
Duration - initially 10 months, likely to be internalised or extended.
Your mission:
• You create, test and optimize the automated production process. You are jointly responsible for automation right from the planning and engineering phase.
• You create recipes in DeltaV and monitor them during the run-in, qualification and production phases.
• You take part in risk and process deviation analyses.
• In collaboration with the plant team, you ensure documentation in accordance with cGMP.
• You continuously improve procedures and processes in compliance with safety, hygiene, environmental and quality requirements.
• Ability to identify risks related to safety or compliance/GMP and take measures to remedy them.
• Partial home office work is possible once you are established in the role.
Your background:
• Fluent German skills, with conversational English – team is German speaking, some colleagues are US-based.
• 3+ years of bioprocess recipe writing experience.
• Completed degree or training in the fields of biotechnology, chemistry, chemical engineering, biopharmaceutical sciences or a similar field.
• Very good understanding and experience in writing recipes in MES SYNC and/or DeltaV.
• Strong background in bioprocess engineering, or automation engineering with biopharma experience.
• Good understanding of IT process controls.
• Able to understand risk in GMP compliance when writing recipes.
• Strong team player and very good communication style.
• Ability to identify risks related to safety or compliance/GMP and take measures to remedy them.
What's on offer
• An initially 10 month contract, likely to be extended or internalised.
• A great opportunity to develop your career at a leading international biotechnology company.
• A competitive salary.
If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: hugo.palejowski@swisslinx.com.
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