DSP Manufacturing Process Expert/Bioprocess Engineer (m/f/d) — Coopers Group AG
- Location
- Sion
- Contract
- contracting
- Posted
- 4 days ago
Role overview
The role serves as the manufacturing subject matter expert for assigned products, ensuring compliant, safe, efficient, and reliable production according to cGMP requirements, regulatory expectations, and operational excellence standards.
The DSP Bioprocess Engineer acts as the Functional Lead for manufacturing-related activities, supports plant operations, leads risk assessments and process improvements, and provides technical expertise for capital projects, commissioning, qualification, and operational readiness. Contract start date: Immediately Contract end date: 31 Jan 2027 Location: Visp
- The role serves as the manufacturing subject matter expert for assigned products, ensuring compliant, safe, efficient, and reliable production according to cGMP requirements, regulatory expectations, and operational excellence standards.
- The DSP Bioprocess Engineer acts as the Functional Lead for manufacturing-related activities, supports plant operations, leads risk assessments and process improvements, and provides technical expertise for capital projects, commissioning, qualification, and operational readiness. Contract start date: Immediately Contract end date: 31 Jan 2027 Location: Visp
- Key Responsibilities Manufacturing Operations
- Plan, coordinate, execute, and document manufacturing campaigns within the assigned DSP production area.
- Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or a related discipline.
- Relevant experience in biopharmaceutical manufacturing, downstream processing, process engineering, or technical operations.
Main responsibilities
- Key Responsibilities Manufacturing Operations
- Plan, coordinate, execute, and document manufacturing campaigns within the assigned DSP production area.
- Ensure manufacturing activities are performed in accordance with cGMP guidelines, approved procedures, and regulatory requirements.
- Support batch execution through process monitoring, evaluation of test results, issue resolution, and troubleshooting of manufacturing equipment and processes.
- Identify and implement corrective and preventive measures to ensure reliable and efficient manufacturing performance. Product and Process Ownership
- Serve as Functional Lead for all manufacturing aspects of assigned products.
- Lead and coordinate multidisciplinary teams to ensure successful execution of manufacturing campaigns.
- Ensure manufacturing processes, equipment, and facilities remain aligned with current industry standards and regulatory expectations.
- Drive technical expertise and process knowledge within the assigned production area. Risk Management and Compliance
- Prepare, facilitate, and execute SHE (Safety, Health and Environment), Environmental Monitoring (EM), operational, cleaning, and product-specific risk assessments.
Key requirements
- Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or a related discipline.
- Relevant experience in biopharmaceutical manufacturing, downstream processing, process engineering, or technical operations.
- Experience working in a cGMP-regulated environment preferred.
- Strong knowledge of biopharmaceutical manufacturing and downstream processing operations.
- Sound understanding of cGMP regulations and regulatory expectations.
- Experience in risk management, deviation handling, CAPA, change control, and validation activities.
- Strong technical troubleshooting and problem-solving skills.
- Excellent communication and stakeholder management abilities.
- Project leadership and cross-functional collaboration skills.
- Ability to work effectively in a dynamic and highly regulated manufacturing environment. Candidates • Coopers Portal Coopers Care Specialization Placements Contracting Payrolling Refer a Friend
Additional details
- The DSP Bioprocess Engineer acts as the Functional Lead for manufacturing-related activities, supports plant operations, leads risk assessments and process improvements, and provides technical expertise for capital projects, commissioning, qualification, and operational readiness. Contract start date: Immediately Contract end date: 31 Jan 2027 Key Responsibilities Manufacturing Operations
- Identify and implement corrective and preventive measures to ensure reliable and efficient manufacturing performance. Product and Process Ownership
- Drive technical expertise and process knowledge within the assigned production area. Risk Management and Compliance
- Ensure compliance with applicable cGMP, EHS, quality, and regulatory requirements. Documentation and GMP Systems
- Support audit readiness through accurate and complete documentation practices. Training and Operational Support
- Promote a culture of operational excellence, quality, safety, and continuous learning. Capital Projects and Facility Readiness
- Support successful transfer of new technologies, products, and manufacturing processes into routine operations. Continuous Improvement and Innovation
- Identify opportunities to improve safety, quality, productivity, robustness, and operational efficiency. Customer and Regulatory Interaction
- Ability to work effectively in a dynamic and highly regulated manufacturing environment.
Notes and original content
- The DSP Bioprocess Engineer acts as the Functional Lead for manufacturing-related activities, supports plant operations, leads risk assessments and process improvements, and provides technical expertise for capital projects, commissioning, qualification, and operational readiness.
- Contract start date: Immediately
- Contract end date: 31 Jan 2027
- Location: Visp
- Key Responsibilities
- Manufacturing Operations
- Identify and implement corrective and preventive measures to ensure reliable and efficient manufacturing performance.
- Product and Process Ownership
- Drive technical expertise and process knowledge within the assigned production area.
- Risk Management and Compliance
Questions about this listing
What salary does Coopers Group AG offer for this role?
Coopers Group AG lists CHF 60'500 - 91'500 gross per year for this position in Sion. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Coopers Group AG offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Coopers Group AG during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Valais?
EU/EFTA residents living in the border zone of the country adjoining Canton Valais can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Valais's cantonal migration office or with HR during the application.
How do I apply for this position at Coopers Group AG?
Use the "Apply now" button on this page — it links directly to Coopers Group AG's original listing at coopers.ch, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
