Your newpany
You’ll be joining a highly respected biopharmaceutical organisation in Wrexham, operating within a fully GMPpliant manufacturing environment. Thepany partners closely across functions such as Supply Chain, Production, QC, and Industrialisation to ensure high‑quality materials are released on time, supporting critical manufacturing operation.
Your new role
As a QC Iing Technician, you will be responsible for assessing and approving all iing raw materials andponents that require Quality inspection. Your role includes sampling and testing materials, performing analyses to pharmacopoeial and licence requirements, entering and reviewing data in LIMS and SAP, and ensuring all activities meet GMP, GLP, and regulatory standards. You’ll also support audits, maintainpliant documentation, conduct GMP housekeeping, and escalate any issues promptly.
What you'll need to succeed
1. Experience working within a GMP or regulated laboratory environment
2. Strong understanding of raw material testing, sampling, and iing goods assessment
3. Ability to interpret pharmacopoeial methods and ensurepliance
4. High attention to detail with a right first‑time approach to documentation
5. Strongmunication skills to collaborate with Supply Chain and other internal teams
6. HND in a scientific discipline or equivalent experience
What you'll get in return
You’ll join a supportive QC Operations environment where accuracy,pliance, and continuous improvement are valued. You’ll gain exposure to cross‑functional collaboration, contribute to material release for vital pharmaceutical manufacturing activities, and develop deeper expertise in GMPpliant Quality Control processes.