Descripción de la oferta
Overview A well‑established CRO operating within a GMP/GLP environment is expanding its biopharma team and seeking a Scientist to support technology transfer and validation activities across both small and large molecule products. Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada. This role offers broad analytical exposure within a regulated setting. Candidates currently working at Analyst level and looking to progress into a Scientist role are welcomed. Applicants may come from industry or investigational/research backgrounds. Key Responsibilities Design, supervise, and execute analytical method transfer and validation studies Perform and support analytical testing for biologics and small molecule products Ensure all activities comply with GMP and/or GLP requirements Prepare, review, and maintain technical documentation Collaborate with internal teams to deliver projects to agreed timelines Requirements Bachelor\'s degree in Chemistry, Biochemistry, Biotechnology, or a related scientific discipline 1–2 years\' experience in a pharmaceutical, biotech, or CRO environment (industry or research considered) Strong hands‑on experience with HPLC (essential) Experience with biologics and/or small molecule analytics (both preferred; one considered) Understanding of GMP principles (GLP considered) Clear communication skills and ability to work in a regulated environment Language Requirements: English and Spanish at strong conversational level (English minimum B2) 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. Equal Opportunities 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. #J-18808-Ljbffr
