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Proclinical is partnering with a highly innovative biotechnology organization that is part of a leading global biopharmaceutical group. The company is at the cutting edge of next-generation in vivo cell and gene therapies, with a particular focus on novel lentiviral vector platforms designed to transform how therapies are delivered and manufactured. Combining the agility of a research-driven biotech with the scale and resources of a major pharmaceutical organization, this is a collaborative, science-first environment where creativity and technical excellence are encouraged, and where discovery work has a clear line of sight to patient impact. The Opportunity: Proclinical is seeking a Director, Process Innovation to lead discovery-stage process development and analytical innovation for an emerging lentiviral vector platform. This is a strategic leadership role focused on early-stage process design, platform building, and technical de-risking, rather than routine manufacturing or late-stage CMC. You will play a critical role in shaping how vectors are produced, characterized, and translated from bench to scalable bioreactor systems - creating the technical foundation that future CMC teams will build upon. This position can be based in Massachusetts, United States, Belgium or in Cambridgeshire, United Kingdom. Why This Role Matters: This is a rare opportunity to shape how future in vivo cell therapies are made - defining new technical standards, enabling innovative platforms, and accelerating the path from discovery to scalable therapies that could transform patient care.
Job Responsibility:
Define and drive the vision for early process innovation in lentiviral vector production
Design and optimize processes suitable for small-scale bioreactor manufacturing
Lead the development of fit-for-purpose analytical methods to assess vector quality, potency, and consistency at the discovery stage
Support the engineering of novel production cell lines to enable next-generation vector platforms
Collaborate closely with discovery scientists, CMC, QA, and external CDMOs to ensure alignment and future tech-transfer readiness
Provide expert technical judgment, critically evaluating experimental plans, data packages, and external deliverables
Build, mentor, and inspire a high-performing team that values innovation, rigor, and accountability.
Requirements:
MSc or PhD in Virology, Biochemistry, Cell Biology, Molecular Biology, Biomedical Engineering, or a related discipline
Proven years of industry experience in bioprocess development and analytical sciences, ideally within viral vectors
Proven leadership in early-stage process development, preferably with lentiviral systems
Experience working with and overseeing CDMOs or external manufacturing partners
Solid understanding of regulatory expectations for gene or cell therapy CMC development
Strong communication skills, collaborative mindset, and a passion for advancing transformative medicines.