Process Technician

Description:

Your 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 timesThis 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 environmentDesirable:

Experience in bioprocessing (upstream/downstream)
Exposure to validation, qualification, or environmental monitoring activitiesWhat 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 rolesWhat 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