Title: CMC Manager
Location: United Kingdom
Duration: 12-month contract (100% attendance)
Company Overview
Apsida Life Science is currently partnering with a clinical-stage biotechnology company that is developing a potent, selective, and orally bioavailable small-molecule.
Responsibilities
- Support overall CMC program execution for Phase 3 readiness and commercial planning activities
- Develop and maintain integrated CMC timelines, project plans, risk registers, and action trackers
- Coordinate cross-functional meetings with internal stakeholders and external partners
- Track project deliverables and ensure alignment with regulatory and clinical milestones
- Prepare meeting agendas, minutes, and follow-up actions for governance and technical meetings
- Support inspection readiness and due diligence activities as needed
- Budget & Financial Tracking
- Manage and track CMC-related budgets, purchase orders, invoices, and accruals
- Monitor spending against forecasts and support annual budgeting exercises
- Coordinate with Finance and external vendors to ensure timely processing of contracts and invoices
- Assist with vendor selection and management activities
Clinical Supply & Logistics
- Coordinate clinical supply manufacturing schedules, supply of raw materials and shipping logistics
- Manage shipment planning for drug substance, drug product, reference standards, and critical materials
- Work with Supply Chain and Clinical Operations to support global clinical trial requirements and commercial supply planning
- Ensure appropriate documentation for import/export, temperature monitoring, chain of custody, and GMP compliance
- Support inventory tracking and reconciliation activities
Qualifications
- Bachelor’s degree in chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or related discipline
- 5+ years of experience in CMC, Technical Operations, Manufacturing, Supply Chain, or Pharmaceutical Project Management
- Experience supporting clinical-stage small molecules
- Demonstrated experience managing external CDMOs and cross-functional projects
- Strong organisational and project management skills with the ability to manage multiple priorities simultaneously
- Familiarity with GMP regulations and pharmaceutical development processes
- Excellent communication and interpersonal skills
- Proficiency with Microsoft Office, project management tools, and budget tracking systems
If you are interested in learning more, please reach out to Sweetness Zono at Apsida Life Science:
www.apsida.co.uk
+44 (0) 744 134 2281
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 and trusted recruitment service that puts the candidate journey at the heart of the recruitment process
