Transfer Specialist - Reagent Manufacturing Operations (GMP, Life Sciences/Pharma/Biotech)

Dawar Consulting

  • Tucson, Arizona
  • 30+ days ago

    Highlights

    Seeking a Transfer Specialist to support the transfer of new tissue diagnostic assays, reagents, and bulk materials from R&D into commercial manufacturing. Our client, a world leader in biotechnology and gene therapy, is looking for an “Transfer Specialist - Reagent Manufacturing Operations” based in Tucson, AZ.

    Numbers & Facts

    LocationTucson, Arizona
    Websitewww.dawarconsulting.com

    Description

    Our client, a world leader in biotechnology and gene therapy, is looking for an “Transfer Specialist - Reagent Manufacturing Operations” based in Tucson, AZ.

     

    Job Duration: Long Term Contract (Possibility Of Extension)

    Pay Rate : $32/hr on W2

     

    Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

     

    Seeking a Transfer Specialist to support the transfer of new tissue diagnostic assays, reagents, and bulk materials from R&D into commercial manufacturing. This role focuses on cross-functional project coordination, technical transfer, GMP compliance, and continuous process improvement. This is not a laboratory role, but a Life Sciences background is required to effectively collaborate with technical teams.

     

    Key Responsibilities

    • Coordinate product and process transfers from R&D to Manufacturing, ensuring quality, cost, and schedule objectives are met.
    • Collaborate with Operations, Development, Regulatory, Validation, and Project teams to support successful product launches.
    • Track project milestones, manage documentation, and support process validation activities.
    • Ensure compliance with cGMP, SOPs, quality systems, and regulatory requirements.
    • Support audit readiness, NCR investigations, and corrective actions.
    • Apply Lean principles and basic problem-solving tools to improve manufacturing processes.
    • Prepare technical documentation, reports, and standardized procedures.
    • Manage multiple project deliverables while communicating effectively with cross-functional stakeholders.

     

    Required Qualifications

    • Bachelor's or Master's degree in Life Sciences (Biology, Chemistry, Biochemistry, Physiology, or related field).
    • 1+ year of experience in pharmaceutical, biotechnology, medical device, or other regulated industries.
    • Experience coordinating projects or deliverables across multiple stakeholder groups.
    • Working knowledge of cGMP/GMP environments and SOP compliance.
    • Strong communication, stakeholder management, organizational, and problem-solving skills.
    • Familiarity with Lean principles; Six Sigma and Minitab experience are a plus.

     

     

    If interested, please send us your updated resume at

    hr@dawarconsulting.com

    /

    akansha@dawarconsulting.com


     

     

     



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