CMC Consultant

Title: Freelance Regulatory CMC Consultant Location: Remote (Italy and travelling to UK Sites twice in a year) Commitment: Minimum 50% time (Iterative, deadline-driven)

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Company Overview

Apsida Life Science is currently partnering with a clinical-stage biotech based in Turin, Italy, developing inhaled peptide therapeutics for respiratory diseases and oncology.

Responsibilities:

Directly author and own CMC regulatory submissions, including IMPDs, INDs, and CTAs. This requires hands-on writing of dossiers and scientific documents, not just oversight. CDMO Management: Act as the primary point of contact for external CDMOs, managing day-to-day operations, project schedules, and budgets for Drug Substance (DS) and Drug Product (DP). Supply Chain & Logistics: Partner with Clinical Operations to project DS/DP needs and manage the end-to-end supply chain to support preclinical and clinical studies. Technical Review: Lead the review of critical process documentation, including batch records, protocols, CoAs, specifications, deviations, and change controls. Strategic Planning: Identify and select CDMOs for development, optimization, and scale-up across the company portfolio. Cross-functional Integration: Align CMC project management with non-clinical and clinical development functions to ensure information flow and compliance with cGMP standards.

Qualifications:

BSc, MSc, or PhD in Life Sciences. 7–10+ years in Biotech, Pharma, or CDMO environments within a CMC/Analytical function. Essential experience in sterile liquid formulation development, specifically targeting shelf-stable presentations. Proven experience drafting and submitting IMPDs/INDs and navigating tech transfer/scale-up. Direct experience with small peptide development, peptide formulation, and associated analytical methodologies. Deep fluency in cGMP standards, ICH guidelines, and regulatory requirements for DS/DP manufacture. xpavfwm Availability to travel to Torino once every two months for 2-4 days Availability to visit manufacturing sites in Italy and the UK (twice/year)

If you are interested in learning more, please reach out to Sweetness Zono at Apsida Life Science:

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Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost-effective, high-quality, and trusted recruitment service that puts the candidate journey at the heart of the recruitment process