IGI
Senior CMC Project Lead
Skills
21 days ago
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Important information
Contract type:
Permanent
Location:
Neuchâtel, Switzerland
Work mode:
Onsite
Published on:
5 October 2026
What they need
You will oversee a part of the CMC development activities and GMP manufacturing for our innovative bi-/multi-specific antibody programs, working closely with CDMOs, CROs, and cross-functional internal teams to ensure successful delivery of development milestones.
Key Responsibilities
- Lead a part of the CMC development activities including Cell Line Development, Upstream & Downstream Processing, Formulation, and Analytical Development through external partners.
- Oversee a part of the GMP manufacturing of drug substance and drug product for clinical programs.
- Serve as the primary point of contact for CDMOs and CROs, managing outsourced activities, timelines, and deliverables.
- Drive technology transfer and external manufacturing activities as a key member of project teams.
- Partner with CMC Strategy, Regulatory Affairs, and Project Management teams to ensure robust supply planning and regulatory readiness.
- Present project progress, risks, and mitigation plans to senior leadership and stakeholders.
- Contribute to budget planning, forecasting, and critical CMC documentation.
We are seeking a collaborative and results-oriented professional with:
- Strong experience in biologics CMC development and external manufacturing management.
- Proven ability to manage complex cross-functional projects and external partnerships.
- Excellent communication, stakeholder management, negotiation, and problem-solving skills.
- Experience working within a global, dynamic, and innovative environment.
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