Jobs

    Materials Planning Manager - California, United States - Life Science People

    Life Science People
    Life Science People California, United States

    2 weeks ago

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    Description

    Material Planner - Cell Therapy Portfolio

    Company Overview: Join an innovative pharmaceutical company at the forefront of cell therapy advancements. They are committed to transforming patient care through cutting-edge treatments and therapies.

    Position Overview: My client is seeking a highly motivated Material Planner to oversee the planning and procurement of materials essential for the production of their cell therapy products. The ideal candidate will possess a strong background in material planning within the pharmaceutical industry, with a focus on cell therapy or biologics manufacturing.

    Key Responsibilities:

    • Develop and execute material plans to support cell therapy production schedules, ensuring on-time delivery and optimal inventory levels.
    • Collaborate closely with cross-functional teams including manufacturing, quality, and supply chain to assess demand forecasts and ensure alignment with production goals.
    • Monitor inventory levels and implement strategies to minimize excess or obsolete inventory while maintaining continuity of supply.
    • Identify and mitigate potential risks to the supply chain, proactively resolving issues related to material availability or quality.
    • Establish and maintain relationships with key suppliers, negotiating contracts and terms to optimize cost and quality.
    • Utilize ERP systems and other planning tools to track materials, monitor order status, and generate reports for management review.

    Qualifications:

    • Bachelor's degree in supply chain management, business administration, or related field.
    • Minimum of 3 years of experience in material planning, procurement, or supply chain management within the pharmaceutical industry.
    • Prior experience with cell therapy manufacturing highly preferred.
    • Strong understanding of cGMP regulations and quality standards applicable to pharmaceutical manufacturing.
    • Proficiency in ERP systems and Microsoft Office suite.


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