Your newpany
You will be joining a well-established and expanding pharmaceutical manufacturer based in North Wales, operating within a highly regulated GMP environment. The site has recently undergone significant investment and continues to grow, supporting the production ofplex drug substances within a collaborative and quality-driven setting.
Your new role
As a Pharmaceutical Process Technician, you will play a key role in supporting manufacturing operations across both upstream and downstream processes. This is a hands-on position within a cleanroom environment, working closely with production, quality, and engineering teams.
Key responsibilities will include:
1. Executing GMP manufacturing activities such as media preparation,ponent transfers, upstream/downstream processing, and equipment cleaning.
2. Accuratelypleting batch records and GMP documentation in real time, ensuring fullpliance with regulatory standards
3. Operating process equipment in line with SOPs and validated procedures
4. Supporting validation and qualification activities, including protocol execution and data recording
5. Carrying out basic preventative maintenance and equipment checks to ensure operational efficiency
6. Participating in environmental monitoring, sampling, and facility checks
7. Contributing to deviation investigations, CAPAs, and continuous improvement initiatives
8. Maintaining high standards of health & safety and GMPpliance at all times
This is a shift-based role, requiring flexibility across early and late patterns, with occasional weekend work.
What you'll need to succeed
To be successful in this role, you will have:
9. A degree in a Life Sciences discipline ( Biotechnology, Chemistry, Biology) or equivalent hands-on experience
10. Prior experience working in a GMP regulated environment, ideally within pharmaceutical or biopharmaceutical manufacturing
11. Exposure to cleanroom environments and controlled processes
12. A strong understanding of GMP principles, documentation, andpliance standards
13. High attention to detail with a methodical and process-driven approach
14. The ability to follow strict procedures and work effectively within a team-based manufacturing environment
Desirable:
15. Experience in bioprocessing (upstream/downstream)
16. Exposure to validation, qualification, or environmental monitoring activities
What you'll get in return
17. Opportunity to gain experience within a growing pharmaceutical manufacturing site
18. Exposure to regulated GMP processes and validation activities
19. A collaborative working environment with strong technical teams
20. Valuable experience to support progression into manufacturing, validation, or quality roles