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A leading pharmaceutical company in Beeston is seeking individuals for the Analytical Services Team. Responsibilities include supporting analytical testing and method development in line with GMP regulations. Candidates should possess a degree in a scientific discipline and experience in a GxP laboratory. The role offers a competitive salary and excellent benefits, including holidays, bonuses, and training opportunities.
Upperton Pharma Solutions is a Nottingham-based CDMO that specialises in the development and manufacture of pharmaceutical products, providing a complete service from early-stage feasibility to GMP clinical manufacture. Formulations cover a range of delivery routes, typically including oral (tablets & capsules), nasal, and inhaled.
Continued growth and investment into the business has led to the creation of exciting new job opportunities in our new GMP Manufacturing headquarters in Beeston, Nottingham. Upperton Pharma Solutions is undergoing a period of significant expansion to meet international customer demand and offer a comprehensive drug development portfolio, so now is a great time to join our team.
Our values ensure that you will be joining a team with a truly positive and progressive culture surrounded by state-of-the-art facilities where you, as a leader, can share your ideas with other gifted and dedicated scientists and clients from around the world, all focused on developing new medicines.
The Role
Based in the Analytical Services Team, the post holder will be directly involved in all aspects of analytical testing to support Development, Tech Transfer, and QC/GMP projects. The post holder will be primarily laboratory-based and will support the analytical aspects of a project focusing on the development and qualification/validation of analytical methods. The post holder will be expected to work to cGMP.
Main Duties And Responsibilities
Undertake practical and written project work as directed, using the company's processes safely to meet GMP requirements.
Work independently in the Laboratory under GMP regulations.