QC Analyst

ROLE OVERVIEW We are currently looking for QC Analysts to join a leading pharmaceutical company’s Quality Control Laboratory, based in a dynamic and regulated environment. This is an exciting opportunity for proactive and detail-oriented individuals to contribute to high-quality testing and compliance within a busy laboratory setting. As a vital part of our client’s QC team, you will be responsible for executing laboratory tests, supporting investigations, and ensuring data integrity and GMP compliance. This role offers a chance to develop your skills in a high-performance environment, working closely with experienced professionals who are committed to quality and excellence. KEY DUTIES AND RESPONSIBILITIES Your duties as the QC Analyst will be varied; however, the key duties and responsibilities are as follows: Conduct laboratory testing in line with EU GMP and MHRA guidelines to produce accurate and reliable data. Assist in the review, maintenance, and improvement of Standard Operating Procedures (SOPs). Prepare samples, standards, and reagents according to documented procedures, ensuring proper recording and data integrity. Maintain and operate laboratory equipment such as pH meters, titrators, HPLC, and GC systems, ensuring they are calibrated and fit for purpose. As the QC Analyst, you will participate in internal audits, regulatory inspections, and support investigation of Out-of-Specification (OOS) results. ROLE REQUIREMENTS To be successful in your application to this exciting role as the QC Analyst, we are looking to identify the following on your profile and past history: A Degree or higher level in Chemistry, Biology, Pharmacy, or a related scientific field. Proven experience working within a pharmaceutical environment, preferably with exposure to raw materials and finished product testing. Good understanding of GMP, SOPs, Health & Safety policies, and relevant regulatory guidelines such as MHRA and EU GMP. Demonstrable knowledge of QC testing techniques, including instrument-based methods like HPLC and GC, and wet chemistry methods. WHAT’S IN IT FOR YOU? This position offers a competitive salary band with Grade 1 (£29,000–£32,000) and Grade 2 (£32,001–£34,000) options, complemented by opportunities for professional growth within a reputable organisation. You will work in a supportive environment that values quality, compliance, and continuous development, making it ideal for those looking to advance their career in the pharmaceutical industry. Key Words: QC / Laboratory / Testing / GMP / MHRA / EU GMP / HPLC / GC / Data Integrity / Regulatory / Investigation / Compliance / Pharmaceutical / Quality Control / SOPs / Calibration / Validation / Health & Safety / Instrument / Wet Chemistry / Analysis "Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career."