- Strong progression opportunities
- Competitive salary offering
About Our Client
The client is a specialist CRO based in London, who are leading the way in testing respiratory and infectious disease vaccines and antivirals. They have an innovative culture, and are able to offer hybrid working arrangements, high salary packages, and good growth opportunities.
Job Description
- Management of QMS documents
- Provide support and advice in relation to SOPs, policies and master forms
- Day to day running of eQMS with support from wider QA team
- Implementing regulatory archiving strategy, and acting as nominated company archivist
- Support wider QA team with audits and inspections
The Successful Applicant
- Demonstrated knowledge within a GCP/GLP QA environment
- Experience in regulatory archiving within a CRO or Pharmaceutical environment
- SOP management experience within CRO or Clinical Trial environment
What's on Offer
- Competitive salary dependant on experience, generally above market average
- Great progression opportunities within a high growth market leader
- This company has a great culture, and is well known for its staff retention and training
