QC Analyst - Raw Materials - FTC 6M

QC Analyst - Raw Materials - FTC 6M Join to apply for the QC Analyst - Raw Materials - FTC 6M role at Ethypharm. This range is provided by Ethypharm. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Location: Romford, onsite role Contract Type: Fixed Term Contract - 6 Months Working Hours: Monday - Friday, 8:00am - 4:00pm, with a 30 minute lunch break. Right to Work: Sponsorship not currently available We are now recruiting an experienced Quality Control Analyst - Raw Materials reporting to the Quality Control Supervisor. Under the guidance of the Quality Control Supervisor, the role holder is responsible for the analysis process in accordance with Current Good Manufacturing Practice (cGMP) at our Romford site. Day‑to‑day responsibilities Analysis of raw materials batches to compendial monographs. 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 to throughout the laboratory. Perform relevant Quality Control responsibilities and ensure laboratory compliance requirements, testing protocols and safety standards are met. About you 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 solid understanding of regulatory standards, and excellent problem‑solving abilities. This role will be based at our Romford office and is an onsite position. Skills / Experience 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 Experience of developing and/or modifying analytical methods within regulatory guidance Prior experience working with British and European Pharmacopeia Demonstrate a 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 What we offer you Holiday - 25 days rising to 30 with length of service plus bank holidays Holiday Buy/Sell - 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) Pension Scheme At Ethypharm we recognise the value of diversity in the workplace and provide equal opportunities for all. Seniority level Entry level Employment type Full-time Job function Analyst, Manufacturing, and Production Industries Pharmaceutical Manufacturing #J-18808-Ljbffr