Unfortunately, we are unable to offer visa sponsorship for this role.
This is a full time, permanent position working 35 hours per week flexibly between 07:00 – 19:00.
As an Analytical Scientist, you will be responsible for performing stability testing on finished pharmaceutical products, ensuring accurate, timely results in line with GMP expectations.
Job Responsibilities that you be covering:
- You will perform routine and non routine analysis of pharmaceutical products using a range of analytical techniques (primarily HPLC, Dissolution, and Karl Fischer).
- You will support technology transfers for new products entering the team, ensuring smooth implementation and alignment with client procedures.
- You will review analytical data for GMP compliance and initiate or follow up on OOS results and action limits when required.
- You will document data in accordance with current client policies and procedures and prepare/approve results for tests in which you are trained and deemed competent.
- You will maintain productivity through agreed metrics (e.g. test numbers, cycle times) and support audits, method revisions, and testing of QC samples.
- You will liaise with client representatives, provide updates to designated personnel, support continuous improvement initiatives, and work flexibly in line with business needs.