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

Dawar Consulting
  • Tucson, Arizona
    30+ days ago

    Job 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


     

     

     



    Numbers & Facts

    LocationTucson, Arizona
    Websitewww.dawarconsulting.com

    Skills

    • Assaysunmatched
    • Biochemistryunmatched
    • Biologyunmatched
    • Biotech and Pharmaceuticalunmatched
    • Chemistryunmatched
    • Communication Skillsunmatched
    • Corrective Actionunmatched
    • Cross-Functionalunmatched
    • Current Good Manufacturing Practice (cGMP)unmatched
    • Delivery Managementunmatched
    • Document Managementunmatched
    • GMP (Good Manufacturing Practices)unmatched
    • Gene Therapyunmatched
    • Maintain Complianceunmatched
    • Manufacturingunmatched
    • Manufacturing Operationsunmatched
    • Manufacturing/Industrial Processesunmatched
    • Medical Equipmentunmatched
    • Minitabunmatched
    • Physiologyunmatched
    • Problem Solving Skillsunmatched
    • Process Improvementunmatched
    • Process Managementunmatched
    • Process Validationunmatched
    • Product Supportunmatched
    • Product/Service Launchunmatched
    • Project Trackingunmatched
    • Project/Program Coordinationunmatched
    • Project/Program Managementunmatched
    • Quality System Requirements (QSR)unmatched
    • Regulationsunmatched
    • Regulatory Requirementsunmatched
    • Research & Development (R&D)unmatched
    • Six Sigmaunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Support Documentationunmatched
    • Technical Writingunmatched

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