Job Description This is a permanent full time position, working a 35 hour week, 7 hours per day flexibly between 7am & 7 pm on 5/7 days as per business needs. The purpose of this job is to perform stability testing of finished pharmaceutical products and produce accurate results within an acceptable timeframe. To perform routine and non-routine analysis using traditional and modern analytical techniques (primarily: HPLC, Dissolution and Karl Fisher determination), as required by the client’s representative. To perform technology transfers on new products entering the team To review analytical data for GMP compliance. To initiate and follow-up OOS results and action limits as per client procedures. To document data as dictated by current client policies and procedures. To collect and measure productivity through agreed metrics such as number of tests performed, cycle times, lab/product issues, number of hours worked per project, etc. To prepare and approve results for tests in which they have received the appropriate training and are deemed competent. To deal with client queries and contact designated personnel, with appropriate support from onsite leadership, with any relevant information or issues relating to test results or the service in general. To keep up to date with any technological or method revisions in their area, ensuring their training is complete and adjusting their work as required with approval from the Lead Analyst. Support local audits as required. To perform testing of QC samples in accordance with client procedures. To revise SOPs as required. To adhere to all client standards in the areas of safety, housekeeping and quality, notifying management of any discrepancies.