QC Chemistry Analyst

Wockhardt; Wrexham; On-site; GBP 26,000 - 38,000; Full time

Benefits offered by this job

Discounts on shopping

Salary sacrifice schemes

Sports and Social club

Subsidised canteen

Free parking

Job summary

Wockhardt in Wrexham is seeking a QC Analyst to design and execute analytical validation and verification for quality control. You will support the department by inspecting and analysing components, raw materials, products and processes to ensure compliance with quality standards.

The role requires strong GMP knowledge, experience with HPLC/UPLC/UV/GC methods, and the ability to take on some supervisory duties in a fast-paced pharmaceutical environment.

Qualifications

• Sound understanding of GMP, Health & Safety and COSHH regulations.
• Experience designing validation/verification protocols and writing validation reports.
• Ability to take on a limited supervisory role would be advantageous.
• Experience in pharmaceutical or equivalent laboratory environment with analytical validation.

Responsibilities

• Design and carry out HPLC/UPLC/UV/GC validation and/or verification.
• Support quality by inspection, sampling and analysis of components, raw materials, products and processes.
• Monitor quality through analytical testing and adherence to quality standards.

Skills

GMP knowledge

Health & Safety COSHH

Supervisory ability

Tools

HPLC

UPLC

UV

GC

Method Validation

Job description

• Hours: Monday to Friday, 8.15am - 4.15pm

Are you a quality driven individual with a keen eye for detail?

Then look no further! A fantastic opportunity has arisen for a QC Analyst to join one of the largest generic pharmaceutical companies in the UK.

A day in the life of a QC Analyst

As a QC Analyst you will design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verification and will support the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis.

What we’re looking for

• A sound understanding of current GMP, Health and Safety and COSHH regulations
• Experience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervision
• The ability to take on a limited supervisory role would be an advantage
• Relevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation.

Why Join Us?

This is an exciting opportunity to develop your career in QC Chemistry, working as part of a supportive and collaborative team. You’ll gain hands‑on experience in analytical testing, quality standards, and laboratory practices within a fast‑paced manufacturing environment, while contributing to the consistent quality and safety of our products.

Wockhardt has a range of benefits on offer for all employees including:

• Rewards platform – discounts on shopping, restaurants, holidays and more
• Salary sacrifice schemes
• Sports and Social club
• Subsidised canteen
• Free parking

You will be working from our Wrexham based site which is home to our MHRA approved sterile injectable manufacturing facility.