General Information
* Duration: until 30.11.2026
* Workplace: Visp
* Working hours: Standard
Our client’s site in Visp, Switzerland is growing and for their Biologics organization, we are seeking experienced Bioprocess Engineers.
Tasks & Responsibilities
* Correct execution of production campaigns in accordance with cGMP guidelines.
* Creation and review of risk assessments and implementation of resulting measures.
* Ensuring batch execution, evaluating test results, troubleshooting issues, rectifying faults in manufacturing equipment, and providing proposals for solutions.
* Comprehensive documentation of processes and process know-how, as well as complete GMP documentation.
* Continuous improvement of processes, equipment, and workflows—in collaboration with various project teams such as R&D—to increase process efficiency and ensure the economic utilization of the equipment.
* Responsible for training employees on assigned products (campaign training), as well as sharing responsibility for staff training regarding cross-project topics and daily operations.
Requirements
* Bachelor’s or Master’s degree in Biotechnology, Life Sciences, Chemical Engineering, or a related field.
* Professional experience in pharmaceutical or biotechnological production, preferably in Operations.
* Understanding of GMP.
* Strong team and leadership skills, as well as excellent communication abilities, are among your strengths.
* Characterized by a cross‑functional, structured, and focused working style.
* Well‑organized and open to new ideas and suggestions.
* Fluent in German or English.
Application Submission Deadline: 26.11.2025
Sounds interesting? Apply Now! We look forward to receiving your application!
Seniority level
* Associate
Employment type
* Contract
Job function
* Other
* Industries: Biotechnology Research and Pharmaceutical Manufacturing
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