Full job descriptionYour new company
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 of complex 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:
*Executing GMP manufacturing activities such as media preparation, component transfers, upstream/downstream processing, and equipment cleaning.
*Accurately completing batch records and GMP documentation in real time, ensuring full compliance with regulatory standards
*Operating process equipment in line with SOPs and validated procedures
*Supporting validation and qualification activities, including protocol execution and data recording
*Carrying out basic preventative maintenance and equipment checks to ensure operational efficiency
*Participating in environmental monitoring, sampling, and facility checks
*Contributing to deviation investigations, CAPAs, and continuous improvement initiatives
*Maintaining high standards of health & safety and GMP compliance 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:
*A degree in a Life Sciences discipline (e.g. Biotechnology, Chemistry, Biology) or equivalent hands-on experience
*Prior experience working in a GMP regulated environment, ideally within pharmaceutical or biopharmaceutical manufacturing
*Exposure to cleanroom environments and controlled processes
*A strong understanding of GMP principles, documentation, and compliance standards
*High attention to detail with a methodical and process-driven approach
*The ability to follow strict procedures and work effectively within a team-based manufacturing environment
Desirable:
*Experience in bioprocessing (upstream/downstream)
*Exposure to validation, qualification, or environmental monitoring activities
What you’ll get in return
*Opportunity to gain experience within a growing pharmaceutical manufacturing site
*Exposure to regulated GMP processes and validation activities
*A collaborative working environment with strong technical teams
*Competitive contract offering with potential for extension beyond initial term
*Valuable experience to support progression into manufacturing, validation, or quality roles
What you need to do now
If you’re interested in this role, click ’apply now’ to forward an up-to-date copy of your CV, or call us now.