Quality control technican

Quality Control (QC) Technician – Biologics - Morning Shift 6am-2pm We are seeking a highly motivated and detail-oriented Quality Control Technician to join our team, specializing in the analysis of biological products. This role involves hands-on laboratory work, project management, and technical oversight in a GMP-regulated environment. Key Responsibilities : Design, supervise, and execute quality control studies for biological products, with a strong focus on chromatography and HPLC techniques. Manage assigned projects, ensuring timely delivery and maintaining direct communication with clients. Oversee the preparation and maintenance of technical documentation, including standard operating procedures (SOPs), certificates of analysis, deviations, OOS reports, and CAPAs . Provide direction and supervision to technical staff, ensuring high-quality experimental execution and compliance with regulatory standards. Requirements : Bachelor’s or Master’s degree in Biochemistry, Biotechnology, Chemistry , or a related field. Minimum of 3 years of hands-on experience with HPLC and chromatography techniques. Proven experience in Quality Control within a pharmaceutical company , with a solid understanding of GMP regulations . Familiarity with electrophoretic techniques, Western Blot, ELISA , and protein quality control is a strong plus. Strong organizational and communication skills. Proficiency in English (written and spoken) is required. About Planet Pharma : Planet Pharma is an American parented Employment Business / Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including : Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion / belief, sexual orientation or age.