We are currently searching for a Manufacturing Specialist for one of our clients, a global bio-pharmaceutical company located in Switzerland.
Responsibilities:
- Execute manufacturing activities in either the Upstream Processing or Downstream Processing area according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution
- Support the preparation of SHE (Safety, Health, environment), EM (Environmental Monitoring), operation and cleaning risk assessment for the assigned products and the implementation and control of defined measures
- Assist document preparation (e.g. electronic batch records, SOPs) specific to the assigned production area
- Review production documentation and work on deviations, change requests and implementation of CAPAs to ensure high-quality GMP standards
- Engage in Capital investment projects for building and commissioning of new manufacturing units as manufacturing expert. Responsible for delivering all input required for the specific set-up, commissioning and qualification of the manufacturing suites and equipment
- Responsible for the training of the manufacturing staff on specific equipment or standard operations
Key requirements:
- Bachelor / Master's degree in Biotechnology, Biology, Biochemical Engineering or related disciplines
- Sound knowledge of biotechnological processes either in the area of microbial and/or mammalian cultivation or in the area protein purification
- Excellent communication skills, team player, driven and solution-oriented
- Fluency in English required, fluency in German required
- Open to work in shift (4-shift system)
- Basic GMP understanding is a plus
For further information about this position, please apply with your CV.
*Please note, only those with the right to work in Switzerland can apply!
