SRG are supporting a Leeds based pharmaceutical company who are looking for an entry level candidate to join their thriving Quality department. This is a fantastic opportunity to get in to the world of pharmaceutical quality, learn from experienced team members with great prospects for continued learning and development after the first 6-12 months.

In this role the QC Analyst will:

Perform physicals testing of finished products, Raw materials & Components

Perform analytical testing of Finished or Stability batches using validated HPLC methods

Perform RM analytical testing or Micro/PET to USP, EP, BP monographs

Identify and report equipment problems for Tech. support resolution

Receive and inspect raw materials & Packaging components

Revise standard quality control operating procedures

Identify and reports quality events & OOS/OOTs to line manager

Ability to document all Chemistry, Micro or packaging analysis following good data documentation practice with minimal supervision

Expanding Proficiency

Trained & competent in multiple analytical instrumentation techniques, including HPLC, GC, Dissolution, conductivity/TOC, FTIR

Ability to perform analysis consistently at a high RFT > 90%

Demonstrates some competencies of QC instrument troubleshooting

Bridging Proficiency

Demonstrates independent data documentation, processing & trend awareness

Ability to review data from physicals tests or basic HPLC or GC assays

Performs report writing with minimal supervision e.g. Micro validation, end of stability reports etc.

QC Assistant Analysts at expanding or bridging proficiency must also be able to demonstrate the following abilities:

Business awareness

Effective Communication

Problem solving

Team Work

Successful candidates will have a BSc with a Chemistry focus and must have the right to work in the UK as this position will not offer sponsorship