Work Schedule

Other

Environmental Conditions

Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed

Job Description

When you join Thermo Fisher Scientific at our Swindon site, you’ll work in a leading UK sterile manufacturing hub. This facility is committed to quality, innovation, and global impact. As part of a growing global organization, you will be empowered to deliver your best work with support and resources.

Responsibilities

Set up and operate bulking and/or aseptic filling lines under strict SOPs and GMP conditions, including liquid and lyophilized product fill-finish operations.Complete all activities required to acquire and maintain a Bronze license badge for production-area access (Grade C/D), including successful requalification every 2 years.Manufacture pharmaceutical products according to cGMP, following Batch Manufacturing Records (BMRs).Operate and maintain equipment to minimize downtime and product waste; support start-up, change-over, cleaning, CIP/SIP activities.Clean and maintain cleanrooms and equipment to regulatory standards; perform airlocks, autoclaving, automated cleaning systems, and maintain aseptic environment integrity.Monitor equipment status, report faults immediately, and support corrective actions to ensure continuous compliance.Support validation processes, new product introductions, and continuous improvement initiatives.Perform required SAP transactions and documentation in line with GMP/site quality systems.Support packaging operations and secondary packaging where required.Enforce rigorously to hygiene and cleanroom requirements (PPE, no permitted contamination: hair products, jewelry, cosmetics, etc.).Work collaboratively across teams (engineering, material handling, QA) to ensure smooth production and high quality standards.

Requirements

Previous experience in a regulated pharmaceutical or sterile manufacturing environment preferred — experience in aseptic fill/cleanroom manufacturing is a strong advantage.Knowledge of GMP regulations (MHRA/FDA), cGMP processes, and cleanroom SOPs desirable.Strong scientific or technical background (science-based qualification or equivalent experience).Proven communication skills and ability to work both independently and within a team.Experience or willingness to embrace Lean/Continuous Improvement practices.Skilled at functioning within a cleanroom environment and maintaining strict hygiene and safety protocols.Comfortable with manual handling, prolonged standing, and shift work if required.

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