Biotechnologist (6616 - KFR)
CTC Resourcing Solutions
Valais, Switzerland
Unknown
2 months ago
N/A
SeniorSource: linkedin
Job Description:
The Life Science Career Network
CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.
Biotechnologist
Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a Biotechnologist for a
Contract position till end of 2025 (with possibility for extension) based in the Valais area, Switzerland.
Main Responsibilities:
- Executes manufacturing activities in the area of Drug Product according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution.
- Provides front line technical and procedural support, working with the manufacturing team.
- Securing each batch is manufactured safely, on time, in compliance with the batch instructions and quality requirements
- Responsible for establishing timely and with high quality the required production documentation (preparation, execution and review of batch records) or other relevant GMP documents for the assigned production area.
- Supports process related investigations and assists in decision making on production issues
- Supports process changes and CAPAs related to processes within required timelines
- Performs training activities of relevant areas as operator and supports others and new joiners.
- Operating, setting up and cleaning production equipment and premises for the production of liquid and freeze-dried drug forms (e.g.: compounding, parts washing, autoclaving, filter integrity testing, visual inspection)
Qualifications and Experience:
- Relevant working/residency permit or Swiss/EU-Citizenship required
- 2-4 years of experience GMP environment on the shopfloor (preferably in sterile manufacturing of Drug Product)
- Fluent in either English or German (preferably both)
- Familiarity with GMP requirements, quality procedures and SOP execution
- Strong team orientation
- Effective communication skills and interaction with a variety of interfaces within the organization
- Structured, focused, and well-organized working attitude
- High motivation and dynamic drive
- IT knowledge and knowledge in SAP and MES is a benefit