Salary
Up to £27000 per annum + flexitime (3.30pm finish), bonus, pension
Location
Tredegar
Job Reference
4739
Job Type
Permanent
Posted Date
22/09/2026
Job Details
Chemistry Graduates: Why You Should Apply
Start your career in a GMP laboratory: You'll join a chemistry testing lab as a QC Technician, learning how raw materials and finished products are tested, how a stability programme runs, and how a QC department stays audit-ready.
Know what you're applying for: Around 80% of this role is project coordination and administration, and 20% is bench work. It suits a graduate who wants to understand the whole testing process, from booking a sample in to issuing the certificate, rather than someone who only wants time on the instruments.
Build your day around you: Flexitime lets you start any time between 7:30am and 9:30am and finish between 3:30pm and 5:30pm. Beat the traffic, or get to the gym while it's quiet.
Grow with a busy lab: New business is coming in fast, and the small project team is set to expand. Technicians who prove themselves can progress towards a QC Analyst role, typically after 12 to 24 months.
Your salary, benefits and hours of work
- £27,000 and annual bonus
- Flexitime: start any time between 7:30am and 9:30am, finish between 3:30pm and 5:30pm
- Monday to Friday days, no weekends or bank holidays
- Shutdown from Christmas to the New Year
- Holidays: 24 days plus 8 bank holidays, increasing with length of service (one extra day for every 5 years, to a maximum of 25 years)
- Full training from day one
What you'll do as a Graduate QC Technician
You'll support the QC project team, keeping samples moving and results getting back to customers on time.
- Book stability and project samples into the QC systems and plan your workload with the Team Leader
- Organise despatch of samples to sub-contract partner laboratories, raising purchase orders and labelling correctly
- Collect and trend data sets, create Certificates of Analysis and draft customer quotes
- Prepare reagents, carry out sensory evaluations and run basic sample analysis to documented procedures and GMP
- Help review pharmaceutical methods and specifications against new versions of the European Pharmacopoeia
- Support the stability programme, technical documentation, consumables ordering and continuous improvement projects
What you'll need to apply
- A BSc in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Science or a closely related chemistry-based degree
- A genuine eye for detail and strong organisational skills
- Good computer literacy (Microsoft Office 365) and willingness to learn new systems
Interested?
Click Apply to find out more, or call the office to discuss.
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