Original Beschreibung
## Head of Supply Chain (f/m/d)
###### Permanent employee, Full-time ·Planegg-Martinsried
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##### Your mission
**Strategy**
* Design and execute the global supply chain strategy across multiple studies and phases to enable drug development balancing agility, cost-efficiency, and regulatory compliance.
* Develop and scale supply chain infrastructure and operations to support early-stage clinical development through to late-stage and commercial readiness.
* Establish best practices and systems for procurement, planning, logistics, and CMO/CRO management, ensuring alignment with Quality, Regulatory, Clinical, and Finance teams.
* Drive operational excellence through KPI tracking, scenario planning, and process improvement.
**Planning**
* Lead collaborative demand planning process to ensure uninterrupted clinical supplies: trial forecasting, procurement, and logistics.
* Oversee end-to-end clinical supply planning: protocol design through manufacturing, packaging, labeling, distribution, and inventory management.
**Sourcing**
* Negotiate and manage global vendor relationships (CMOs, CDMOs, 3PLs) and ensure continuity of supply.
* Execute comparator and combination drug sourcing strategies.
**Compliance and Risk Mitigation**
* Support global regulatory submissions and inspections; ensure all activities meet FDA, EMA, and other international requirements.
* Ensure all suppliers comply with import/export and regulatory standards.
* Oversee quality documentation (Deviations, CAPAs, Change Controls, etc.) and support SOP development and continuous improvement for cGxP compliance.
**Leadership and Management**
* Collaborate cross-functionally with Clinical Ops, Technical Ops, QA, Regulatory, Finance, and Program Teams.
* Build and scale a high-performing supply chain team as the company matures.
* Manage budgets and contracts.
##### Your profile
* Bachelor’s degree in Supply Chain, Life Sciences, Engineering, or related field; MBA or advanced degree preferred. APICS certification or coursework is desired.
* 10+ years of progressive supply chain experience in biotech/pharma, including clinical and commercial-stage leadership.
* Proven expertise in clinical supply operations (IRT systems, labeling, cold chain, reverse logistics, etc.).
* Strong knowledge of GxP, GMP, global regulatory standards (CFR, Annex 13, EU CTR), USP/EP.
* Experience with comparator sourcing and global study blinding practices.
* Must be knowledgeable in US, EU, and ROW clinical supply labeling requirements and the QP review/release/certification process for European clinical supplies.
* Experience with both ambient and cold chain products.
* Skilled in strategic planning, project management, contract negotiation, and vendor management.
* Excellent communication, leadership, and cross-functional collaboration skills.
* Dynamic and energetic, hands-on approach to challenges.
* Willingness to engage in business travel to various company offices, suppliers, and partners as required.
##### Why us?
* Impact & Growth – Be part of a dynamic, goal-oriented company where your contributions truly make a difference.
* Innovation – Work on groundbreaking immuno-oncology therapies with a mission-driven team.
* Collaboration & Culture – Enjoy a multicultural, open, and appreciative work environment and direct communication channels.
* Additional Benefits – Competitive compensation, professional development opportunities, and more!
Join us in shaping the future of cancer therapy!