CK Group are recruiting for a Regulatory Affairs Associate - CMC to join a biopharmaceutical company at their site based in Uxbridge on a contract basis for 12 months.
Salary:
£20.50 per hour PAYE
Regulatory Affairs Associate Role:
- The Senior Associate Regulatory Affairs (CMC) provides varying levels of product support to the Chemistry, Manufacturing and Controls (CMC) function, which is responsible for Module 3 of regulatory submissions across phases of product development from clinical to lifecycle.
- Support may include organizing, managing and executing on regulatory CMC projects and submissions.
- Tasks may include creating and/or maintaining submission timelines and tables of contents, formatting of documents per style guide, scheduling meetings, drafting meeting agendas and minutes, managing document reviews and other tasks as requested.
Your Background:
- Degree in life sciences, biochemistry, or chemistry
- Experience in biopharmaceutical or pharmaceutical industry
- Familiarity with eCTD structure
- Experience in CMC, including preparation of submissions to Agencies
Company:
Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics.
Location:
This Regulatory Affairs Associate role will be based at our clients site in Uxbridge, Greater London.
Apply:
Please quote reference 49952
You must be eligible to work in the UK. Learn more
- Agency: CK Group
- Contact: Lucy Stendall
- Phone: 01246 457733
- Reference: 49952
Website: CK Group
- Posted: 22nd February 2021
- Expires: 22nd March 2021
