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Expired
  • Location: Worthing
  • Salary: Very competitive pay depending on experience
  • Job Type:Contract

Posted about 3 years ago

  • Sector: Quality
  • Contact: Steve Twinley
  • Contact Email: steve.twinley@nextphaserecruitment.com
  • Contact Phone: 01403 216216
  • Start Date: 2021-01-18
  • Job Ref: V-46607
Do you have a QA background from a regulated environment (ideally GMP)? Can you start at short notice in a fixed-term contract for around 4 months (possibly longer)? An urgent position has arisen in the Quality Assurance team of a leading Pharmaceutical company in Worthing, West Sussex, to help support them with a range of QA activities while they move to an electronic QMS. This is a 100% site-based role.
 
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.