Verbatim Pharma are currently working with a Clinical Trial Service company who are looking for a Quality Control Associate to join the team on a permanent basis.
This company has been around for more than 20 years and has seen the industry grow and change over the years and is truly committed to their teams based in the UK, US, and the Netherlands.
This is a great opportunity to further develop your career within quality in the clinical trial sector and expand your experience and knowledge.
The ideal candidate will have high attention to detail, problem-solving skills, and a good understanding of the GMP environment, as well as familiarity with the clinical trial industry.
This role is a full-time onsite position based at their site in Reading.
You must be fluent in English.
While you will need a good understanding of the GMP environment and quality, full training will be provided. This is a great opportunity to enter the clinical trial sector if you are looking to expand your experience.
Your responsibilities will include:
1. Complete clearance inspection before delivery of packaging
2. Perform quality control activities for shipments
3. Confirm staging of appropriate materials through batch numbers
4. Participate in internal audits and liaise with suppliers
5. Maintain structure of retention samples
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