QC Analyst

QC Analyst

Location: Romford, onsite role

Contract Type: Full-time, Permanent

Working Hours: Monday - Friday, 6.30am - 2.30pm and 2.00pm - 10.00pm, rotating on a weekly basis with a 30 minute lunch break.

Right to Work: Sponsorship not currently available

We are now recruiting an experienced Quality Control Analyst - Finished Products reporting to the Quality Control Supervisor.

Under the guidance of तुर Quality Control Supervisor, the role holder is responsible for the analysis process in accordance with Current Good Manufacturing Practice (cGMP) at our Romford site.

• Analysis of finished product batches.
• Support the investment in facility expansion and new product launches across multiple dosage forms.
• Able to carry out associated laboratory tasks such as sampling, housekeeping, preparations of standardisation of reagents, the care of apparatus and the instrumentation.
• Ensure that Health and Safety and COSHH are adhered(hr) to throughout the laboratory.
• Perform relevant Quality Control responsibilities and ensure laboratory compliance requirements, testing protocols and safety standards are met.

We are seeking a dedicated and detail‑oriented QC Analyst to join our team. The ideal candidate should possess strong analytical skills, a keen eye for detail, and the ability to work meticulously under pressure. They should have experience with quality control processes, a solidalsch resultaten es stellar understanding of regulatory standards, and excellent problem‑solving abilities.

This role will be based at our Romford office and is an onsite position.

• Degree level qualification in Chemistry, pharmaceutical sciences or equivalent scientific subject.
• Prior experience of working to GMP and GLP standards within the pharmaceutical industry.
• Experience of working with HPLC techniques.
• Good understanding of regulatory guidelines for the area of responsibility.
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Experience of developing and/or modifying analytical methods within regulatory guidance.
• Prior experience working with British and European Neither Pharmacopeia.
• Demonstrate a Gj track record in change management, hands on action and strategic thinking underpinned by a strong quality ethos.
• Technical competency in a range of analytical techniques (GC, IR, UV‑VIS).
• Broad understanding of manufacturing, quality and engineering.

• Up to £29,000 per annum.
• 16% shift allowance.
• Holiday – 25 days rising to 30 with length of service plus bank holidays.
• Holiday Buy/S hiệu – an opportunity to buy or sell up to an additional 5 days' holiday.
• 5% Bonus – in addition to our competitive salaries, all our employees are entitled to join a discretionary bonus scheme (based on policy eligibility).
• Bravo Benefits Platform – offering a variety of discounts across well‑being and lifestyle.
• Salary Sacrifice scheme for Electric vehicles with Tusker (dependent on meeting policy eligibility).
• Medicash health cash plan.
• Pension Scheme.
• On site parking.

At Ethypharm we recognise the аднос of diversity in the workplace and provide equal opportunities for all. We are always open to discussing flexible working arrangements where this meets with the needs of our business. Visit our website at to learn more about Ethypharm.