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    Quality Control Reference Material Specialist - Dublin, Ireland - Cpl Healthcare

    Cpl Healthcare
    Cpl Healthcare Dublin, Ireland

    2 days ago

    cpl healthcare background
    Description

    Cpl in partnership with our client Pfizer are looking for a Quality Control Reference Material Specialist to join the team at their cutting-edge site in Grange Castle, Dublin for a 12-month fixed term contract.

    Quality Control Reference Material Specialist

    Your role will be in the Quality Control Department at Pfizer Grange Castle as part of a growing and diverse team of friendly and supportive colleagues. You will play a direct role in the production, validation, and distribution of various reference materials and antibody solutions used for testing and releasing Pfizer medications worldwide.

    This is a fantastic opportunity to be part of a top-notch facility dedicated to bringing life-improving therapies to the market.

    Job Purpose

    Support quality control reference standard and control programs for established and new products at Pfizer Grange Castle. Coordinate and carry out tasks to aid in the manufacturing, validation, and supply of reference materials and essential reagents for Quality Control testing while ensuring regulatory compliance for ongoing and upcoming projects.

    About the Role

    • Support all necessary activities for the implementation of new reference material programs for Quality Control at Grange Castle.
    • Ship reference material and vital reagents to external clients using the designated shipping process on-site.
    • Collaborate with both internal and external customers of Pfizer to facilitate the overall reference material management process.
    • Assist in the qualification/re-qualification of reference material and vital reagents in partnership with the Grange Castle QC lab teams and within an IMEX framework.
    • Manage and provide support for critical reagents/reference standard supply and international shipments to ensure uninterrupted supply to all markets, contract manufacturing sites, and health authorities.
    • Utilize the Network RMCR Digital system to handle customer requests, inventories, and schedule tasks for loading new lots.
    • Work with external contract sites to coordinate testing outcomes for re-evaluating current lots and qualifying new lots.
    • Prepare necessary aliquots of antibodies and other required reference materials.
    • Discover avenues for Continuous Improvement and embody Pfizer's ethos to take ownership and lead any initiatives related to driving these improvements.
    • Enforce and uphold appropriate levels of cGMP within the team and advocate for safety awareness and a culture of incident-free work within the area.
    • Execute assigned duties and provide support as directed by the QC Manager.

    About You


    • B.Sc. degree in biological/chemical sciences, business, or a related technical field, or relevant experience in a regulated industry. (Recent graduates will be considered)
    • Strong communication and interpersonal skills.
    • Proven ability to articulate issues and necessary solutions in a positive and proactive manner.
    • Self-driven, self-motivated with a track record of project ownership.
    • Adept at working autonomously and collaboratively in a vibrant, fast-paced setting.
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