Senior Process Scientist
Pubblicato il 15-10-2026 - Chiesi in Roma
Overview As Senior Process Scientist, you will drive the development and manufacturing oversight of LNP-based gene therapy programs within Chiesi Global Rare Diseases. You’ll lead formulation development, screening, and process optimization, partnering with external CROs/CDMOs and internal CMC teams to advance candidates from discovery through clinical development toward launch. You will shape transfer strategies, ensure quality and regulatory readiness, and guide lifecycle improvements. This role offers impact across programs and a chance to shape GT delivery platforms in a collaborative, matrix-driven environment. Retribuzione / Benefits * annual premio scheme * pension * private medical insurance * wellbeing programme * flexible benefits * relocation support Responsabilità * Define and lead formulation development plans for LNP platforms,
including lipid/excipient screening and process development * Oversee external manufacturing activities and tech transfers; select and qualify CROs/CDMOs * Provide technical governance for outsourced work; troubleshoot and drive continuous improvement * Review technical documents (batch records, SOPs, reports) and contribute to regulatory sections (IND, IMPD, IB) * Manage project budgets for CROs/CDMOs/consultants and support lifecycle management * Contribute to GRD/GRD R&D; strategy and cross-functional knowledge sharing * Lead root cause investigations and deviation assessments * Support critical evaluation of external business development opportunities focused on oligonucleotides Requisiti fondamentali * MSc in a relevant field * 5-10 years of biotech/pharma experience with exposure to gene editing, CGT/ATMPs and LNP delivery systems * Strong expertise in formulation screening/optimization, process development, scale-up, and tech transfer to GMP manufacturing * QbD-based development (DoE, CPP/CQA identification) and understanding of CQAs * Experience managing outsourced development (CROs/CDMOs) and technical documentation * GMP