Requirements: English
Company: Planet Pharma
Region: South Holland
One of our most exciting clients are seeking a Senior Process Engineer to join their Drug Product Development team in South Holland, supporting advanced therapy programs, including CAR-T cell products. This is a key technical role focused on late-stage development, process robustness, and commercial readiness. Key Responsibilities: Lead fill-finish process development, ensuring scalability and GMP compliance. Drive stability programs (ICH, in-use) and drug product characterisation. Oversee container closure system qualifications and EL studies. Support technology transfer and global manufacturing scale-up. Collaborate with cross-functional stakeholders including Quality, Regulatory, and Manufacturing. Author technical documents, SOPs, and regulatory content. Your Profile: PhD with 7+ years or MSc with 10+ years in life sciences, biotech, or engineering. Experience with advanced therapy medicinal products (ATMPs), preferably CAR-T or biologics. Strong background in formulation, drug product development, and GMP environments. Proven ability to work in cross-functional global teams. Fluent in English Please click apply or contact David Rowland (Recruiter II) at Planet Pharma for more information: E: Drowland@planet-pharma.co.uk T: +44 20 3928 8381 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.