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- Tasks: Assess and approve raw materials, ensuring quality standards are met.
- Company: Join a respected biopharmaceutical organisation in Wrexham.
- Benefits: Supportive environment with opportunities for cross-functional collaboration and professional growth.
- Why this job: Make a real impact in pharmaceutical manufacturing while developing your expertise.
- Qualifications: Experience in GMP environments and strong attention to detail required.
- Other info: Gain valuable insights into Quality Control processes and regulatory compliance.
The predicted salary is between 36000 - 60000 £ per year.
You’ll be joining a highly respected biopharmaceutical organisation in Wrexham, operating within a fully GMP compliant manufacturing environment. The company partners closely across functions such as Supply Chain, Production, QC, and Industrialisation to ensure high‑quality materials are released on time, supporting critical manufacturing operations.
As a QC Technician, you will be responsible for assessing and approving all incoming raw materials and components 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, maintain compliant documentation, conduct GMP housekeeping, and escalate any issues promptly.
What you’ll need to succeed:
- Experience working within a GMP or regulated laboratory environment
- Strong understanding of raw material testing, sampling, and incoming goods assessment
- Ability to interpret pharmacopoeial methods and ensure compliance
- High attention to detail with a right first‑time approach to documentation
- Strong communication skills to collaborate with Supply Chain and other internal teams
- HND in a scientific discipline or equivalent experience
What you’ll get in return:
You’ll join a supportive QC Operations environment where accuracy, compliance, 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 GMP compliant Quality Control processes.
QC Technician employer: hays-gcj-v4-pd-online
Contact Detail:
hays-gcj-v4-pd-online Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Technician
✨Tip Number 1
Network like a pro! Reach out to people in the biopharmaceutical industry, especially those working in QC. Attend industry events or join relevant online groups to make connections that could lead to job opportunities.
✨Tip Number 2
Prepare for interviews by brushing up on GMP and GLP standards. Be ready to discuss your experience with raw material testing and how you ensure compliance. Show them you know your stuff!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you and tailor your approach to each one.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. It keeps you on their radar and shows you’re genuinely interested.
We think you need these skills to ace QC Technician
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in GMP or regulated laboratory environments. We want to see how your skills match the QC Technician role, so don’t be shy about showcasing your relevant qualifications and experiences!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality control and how your background makes you a perfect fit for our team. Keep it concise but engaging – we love a good story!
Showcase Your Attention to Detail: Since this role requires a high level of accuracy, make sure to demonstrate your attention to detail in your application. Whether it’s through your CV formatting or the way you describe your past roles, we want to see that you take pride in your work.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the info you need about the role and our company there!
How to prepare for a job interview at hays-gcj-v4-pd-online
✨Know Your GMP Basics
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Understand the key principles and how they apply to quality control in a biopharmaceutical setting. This will show that you’re not just familiar with the terms, but that you can apply them in real-world scenarios.
✨Familiarise Yourself with LIMS and SAP
Since you'll be entering and reviewing data in LIMS and SAP, it’s crucial to have a basic understanding of these systems. If you’ve used similar software before, be ready to discuss your experience and how it relates to the role. This will demonstrate your readiness to hit the ground running.
✨Prepare for Technical Questions
Expect questions about raw material testing and pharmacopoeial methods. Brush up on your technical knowledge and be prepared to explain how you would approach sampling and testing. Use specific examples from your past experience to illustrate your expertise.
✨Showcase Your Attention to Detail
In a QC role, attention to detail is paramount. Be ready to share examples of how you've ensured accuracy in documentation and compliance in previous roles. Highlight any processes you’ve implemented to improve quality or efficiency, as this will resonate well with the interviewers.
