What are the responsibilities and job description for the Director Drug Substance External Manufacturing position at Mural Oncology?
Mural Oncology is a clinical-stage immuno-oncology company leveraging its novel protein engineering platform to develop cytokine-based immunotherapies for the treatment of cancer. By combining our expertise in cytokine biology and immune cell modulation with our protein engineering platform, we are developing medicines to deliver meaningful and clinical benefits to people living with cancer. Our mission is to broaden the potential, and reach, of cytokine-based immunotherapies to improve the lives of patients.
Detailed Description :
Mural's Director of Drug Substance External Manufacturing, Supplier Relationship Management (SRM) plays a critical role in enhancing the company's supply chain efficiency and fostering mutually beneficial partnerships with our key suppliers. The role of Drug Substance SRM requires a strategic thinker who will work closely with suppliers to enable strong performance, mitigate risks, foster collaboration and drive value creation. As the main point of contact for supplier relations, the SRM negotiates contracts, ensures supplier compliance and monitors performance to meet both short-term operational needs and long-term organizational strategic objectives. Effective interpersonal, analytical, and negotiation skills are essential, as the SRM seeks to cultivate trust, manage risks, and drive continuous improvement within the supply chain.
Job Responsibilities :
- Support the continued development and implementation of the External Manufacturing operating model and business processes across the external network for Mural.
Act as the manufacturing & business relationship manager for designated Suppliers developing mutually beneficial relationships and accountable to deliver high quality, reliable and efficient supply on time and in full.
Partner with Legal, Finance, Process Development, Quality, External Operations and other SME functions across the internal network to deliver assigned contracts aligned with business goals.
Qualifications :
Experience in life sciences or related industry preferred
General knowledge of and experience working in a GMP environment.
Excellent communication, influencing, collaboration and technical writing skills