<div><h3>About the job Process Development Scientist/Engineer</h3><p><b>Job Title:</b> Process Development Scientist/Engineer<br/><b>Location:</b> Cambridge, UK<br/><b>Department:</b> Process Development<br/><b>Reports To:</b> Process Development Team Lead</p><h3>Company Overview</h3><p>Sartorius is a global leader in providing innovative solutions for the biopharmaceutical industry. Our mission is to empower scientists and engineers to simplify and accelerate progress in life sciences, shaping the future of healthcare. Join our Cambridge team and contribute to groundbreaking advancements in cell and gene therapies, bioprocessing, and cutting-edge biomanufacturing technologies.</p><h3>Position Summary</h3><p>We are seeking a highly motivated and detail-oriented Process Development Scientist/Engineer to join our team in Cambridge. This role focuses on developing, optimizing, and scaling up bioprocesses for cutting-edge therapeutic modalities. You will work collaboratively with cross-functional teams to deliver robust and scalable solutions to meet the needs of our clients in the biopharmaceutical and life sciences sectors.</p><h3>Key Responsibilities</h3><ul><li><b>Process Development:</b> Design, develop, and optimize upstream and downstream bioprocesses for novel therapeutic products, including cell and gene therapies, monoclonal antibodies, and recombinant proteins.</li><li><b>Technology Transfer:</b> Collaborate with manufacturing and R&D teams to ensure seamless transfer of processes from development to GMP production.</li><li><b>Data Analysis:</b> Perform in-depth data analysis and interpretation to support process characterization, ensuring reproducibility and scalability.</li><li><b>Equipment Management:</b> Operate and maintain state-of-the-art bioprocessing equipment such as bioreactors, chromatography systems, and filtration units.</li><li><b>Documentation:</b> Prepare technical reports, protocols, and standard operating procedures (SOPs) in compliance with regulatory requirements.</li><li><b>Collaboration:</b> Work closely with multidisciplinary teams, including quality assurance, regulatory affairs, and product development, to ensure project milestones are achieved.</li><li><b>Innovation:</b> Stay abreast of emerging technologies and methodologies in bioprocessing and recommend improvements to existing workflows.</li></ul><h3>Qualifications and Experience</h3><ul><li>A degree (BSc, MSc, or PhD) in Biochemical Engineering, Biotechnology, Biochemistry, or a related field.</li><li>Hands‑on experience in upstream (e.g., cell culture, bioreactors) and/or downstream (e.g., filtration, chromatography) process development.</li><li>Familiarity with cGMP regulations and biomanufacturing standards.</li><li>Strong analytical skills with experience using software for data analysis (e.g., MATLAB, JMP, or similar).</li><li>Excellent organizational and communication skills, with the ability to work effectively in a collaborative environment.</li><li>Knowledge of process characterization and validation principles is desirable.</li><li>Previous experience in the biopharmaceutical or life sciences industry is highly advantageous.</li></ul><h3>What We Offer</h3><ul><li>Competitive salary and benefits package.</li><li>Opportunity to work on groundbreaking projects in a collaborative and innovative environment.</li><li>Access to continuous learning and development programs.</li><li>A culture that values diversity, inclusion, and sustainability.</li></ul><h3>How to Apply</h3><p>If you are passionate about driving innovation in the biopharmaceutical industry and want to be part of a dynamic team, we’d love to hear from you. Please submit your CV and a cover letter detailing your suitability for the role.</p></div>