Quality Control Scientist

Scientist – Biologics & Advanced Therapies (Quality Control) Shift: Afternoon only (13:30–21:30) Por favor, verifique que tiene el nivel de experiencia y las cualificaciones adecuadas leyendo la descripción completa de esta oportunidad a continuación.Overview A growing life sciences organisation is seeking a Scientist to join its Biologics & Advanced Therapies Quality Control team. This role focuses on analytical method development and validation for complex biologics, including monoclonal antibodies, recombinant proteins, and advanced therapy products. This position is open to candidates from both industrial QC and research or investigational environments, provided they have hands‑on experience with biologics analysis. Key Responsibilities Design, execute, and oversee analytical method development and validation Perform hands‑on analysis using techniques such as HPLC, capillary electrophoresis, ELISA, and protein quantification (BCA, UV) Lead assigned validation studies in line with GMP and ICH requirements Author and review technical documentation, including protocols, validation reports, and SOPs Provide technical oversight and support to Analysts and laboratory staff Collaborate cross‑functionally with Quality Assurance and internal stakeholders Requirements Bachelor's degree or higher in Biochemistry, Biotechnology, Pharmacy, or a related discipline 1–2 years' experience in biologics analysis (industry, research, or investigational settings considered) Hands‑on HPLC experience (essential); biologics techniques highly desirable Understanding of GMP and analytical validation principles (GMP preferred; GLP considered) Background as an Analyst looking to progress into a Scientist role is welcomed Strong written and verbal communication skills Language Requirements English and Spanish at a strong conversational level (minimum B2 in English) 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. xugodme 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.