As a QA Compliance Officer, you will provide Quality guidance and support for GMP production operations. You will work on:
- Batch document review
- Complaints investigations
- Quality technical agreements
- Training documents
- SOP updates and (potentially) some
- Non-Conformance investigations (if you are more experienced)
Candidates will be considered at either a more experienced level (in which case a very generous rate of pay is offered) or at a more intermediate level. Your experience level will be reflected in your pay rate; and the company has set a generous budget for more experienced candidates. Crucially, we need someone with enthusiasm and the ability to pick things up quickly.
Because the company’s processes are currently paper-based, you will be based 100% of the time on site in the Worthing office. The environment is highly controlled and very well set up for social distancing, making it a safe place to work.
We are looking for someone with office-based experience in a Pharmaceutical, Diagnostics, Medical Device or similarly regulated environment, where you have developed strong report-writing, admin and document control skills (potentially up to a senior level). Whilst we will consider science graduates with lower experience, it will be a strong advantage if you have some experience from either a QA function or a similar department (e.g. Reg Affairs) where you need strong attention to detail, excellent communication and the ability to scrutinise documents and data.
Full details will be provided on application.