Job Description
We have an exciting opportunity for you to join a small Stability team based in a Quality Control Laboratory You will be apart of a team who put together and perform stability trials of pharmaceutical products manufactured here at Torbay Pharmaceuticals.
We are looking for a lead analyst to support with the preparation and running of annual commitment batch studies and to assist with leading our established team to perform high quality analytical testing to cGMP standards to assure the Quality, Safety and Efficacy of our products across their shelf life. The role will contribute to ongoing annual testing of Licensed TP Products, in addition to playing a vital part in providing Stability data for the regulatory submission of new products across the globe.
- Performing analysis of stability samples to meet the required standards in compliance with regulations.
- Producing data to assist in the licensing of products for Torbay Pharmaceuticals and maintaining compliance.
- Ensure that the stability programme is followed and that all data is generated to cGMP and the Pharmacetical Quality System
- Ownership for writing annual commitment stability protocols, requesting samples and set-down.
- Create data summary tables and update with results as required.
- Undertaking investigations for out of specification and deviations ensuring compliance to cGMP within agreed timescales.
Torbay Pharmaceuticals - Built by the NHS, Supplying the World
At Torbay Pharmaceuticals you’ll work for a truly unique organisation and alongside the most committed people in the business. We have ambitious plans to grow our business over the next few years and we know that we can’t do that without everyone playing their part. That’s why we believe in the One TP way of working.
Shared responsibility for getting a job done is core to our values and is underpinned by a We can if… attitude. If one team needs help to meet a goal, then the rest of us pitch in to help. It’s just what we do and we only want to work with others who would do that too.
Full details can be found on the attached Job Description. In your application please refer to the person specification/role requirements in your supporting information