Job Description
The Swindon site is a key hub for manufacturing and quality control activities at Thermo Fisher Scientific. Home to specialized teams in production, development, and quality assurance of scientific and pharmaceutical products, the site strictly adheres to GMP standards. It plays a vital role in driving innovation and delivering reliable scientific solutions across the UK and globally.
As a Junior QA Officer at Thermo Fisher Swindon, you will join a team committed to innovation, quality, and operational excellence. You will work in a fast-paced, regulated environment, supporting manufacturing and quality operations for sterile liquid and lyophilized products, including high-potency products and large-volume parenterals (LVP). This role provides hands-on experience in GMP compliance and quality assurance, offering excellent opportunities for growth within a leading global life sciences organization generating $20 billion in revenue.
The Swindon facility specializes in coordinated sterile product development and commercial manufacturing, supporting liquid vials, lyophilized products, and complete fill-finish processes. The site has extensive capabilities for primary and secondary packaging and plays a central role in delivering high-quality pharmaceutical products worldwide.
You will support the Quality Operations team across manufacturing facilities and support functions, performing critical tasks to ensure compliance with cGMP standards. Key responsibilities include preparing and managing GMP documents, conducting independent visual inspections of sterile products, and ensuring timely delivery of documentation to clients. Attention to detail and adherence to regulatory and safety standards are essential for success in this role.
