Project Coordinator - IT - III

Iconma LLC

  • Foster City, CA
  • 14 days ago
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    Skills

    • Biotech and Pharmaceuticalunmatched
    • Change Controlunmatched
    • Change Managementunmatched
    • Contract Managementunmatched
    • Contract Manufacturingunmatched
    • Cross-Functionalunmatched
    • Current Good Manufacturing Practice (cGMP)unmatched
    • Document Managementunmatched
    • Documentationunmatched
    • Drug Developmentunmatched
    • Drug Productsunmatched
    • File Maintenanceunmatched
    • Health Planunmatched
    • Manufacturingunmatched
    • Manufacturing/Industrial Processesunmatched
    • Medical Equipmentunmatched
    • Product Controlunmatched
    • Product Managementunmatched
    • Project/Program Coordinationunmatched
    • Project/Program Managementunmatched
    • Regulationsunmatched
    • Riskunmatched
    • Risk Managementunmatched
    • Surveillanceunmatched
    • Time Managementunmatched

    Description

    Our client, a Biopharmaceutical company, is looking for a Project Coordinator - IT - III for their Foster City, CA location.

    Responsibilities:

    • The Device Engineering team at client is seeking a qualified individual to support drug device combination products throughout the commercial lifecycle.
    • This individual will be responsible for the management of combination product change records.
    • Additional responsibilities include post market surveillance reports, risk management file maintenance, and general project management across the combination product portfolio.
    • Coordinate and manage combination product change control records -
    • Initiate, route, and close change records for product and manufacturing process changes.
    • Initiate, route, and close change records for the design and development of drug device combination products, including the creation and management of design control documentation.
    • Manage implementation of changes at multiple manufacturing sites and change record closures.
    • Coordinate post-market surveillance reports and risk management file updates -
    • Collate surveillance information into yearly reports.
    • Generate annual risk summaries and update risk management files.
    • Support complaint investigations and documentation.
    • Act as a central hub between cross-functional teams to ensure supply continuity.

    Requirements:

    • Exceptional organizational and time management skills.
    • Understanding of change controls in a regulated industry.
    • Experience with project management.
    • Working knowledge of relevant US, EU, and international medical device and pharmaceutical regulations.
    • Experience with Veeva Vault.
    • Ability to work with team members, vendors, suppliers, and contract manufacturers to coordinate changes.
    • 3 - 5 years relevant experience in related field and a BS or BA.
    • Experience with medical device development and / or pharmaceutical operations (cGMP environment) required.

    Why Should You Apply?

    • Health Benefits
    • Referral Program
    • Excellent growth and advancement opportunities

    Numbers & Facts

    LocationFoster City, CA

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