SciPro have partnered with a global pharmaceutical business who are looking for a Senior Specialist in QA Operations to join their team in Switzerland. The company are focused on developing innovative solutions to transform the lives of patients through their pioneering technology. With an expansive pipeline, the organization works across a number of therapeutic areas including haematology, oncology and cardiovascular diseases. This role will be a part of the QA Operations team, supporting their manufacturing site in Switzerland and working on cross-functional projects to ensure cGMP compliant production, testing and release of the product.
- Support the CAPA process
- Perform batch record review and prepare batch release documentation
- Bulk manufacturing, semi-finished and finished goods production and warehousing
- Change Control handling
- At least 5 years of experience within pharmaceuticals or related industry
- Good understanding of cGMPs and FDA regulatory requirements
- Good understanding of solid oral dosage form manufacturing processes would be beneficial
- Fluent in French and English
- Ability to manage a conflicting workload independently as well as working collaboratively across different functions to meet business objectives
If you are interested in this opportunity, please apply with an updated CV and contact details.