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

Dawar Consulting

  • Tucson, Arizona
  • 30+ days ago
  • $32 Per Hour

Highlights

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

Numbers & Facts

LocationTucson, Arizona

Description

Our client, a worldleader in biotechnology and gene therapy, is looking for an “TransferSpecialist - Reagent Manufacturing Operations” based in Tucson, AZ.

Job Duration: LongTerm Contract (Possibility Of Extension)

Pay Rate : $32/hr on W2

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

Seeking a TransferSpecialist to support the transfer of new tissue diagnostic assays, reagents,and bulk materials from R&D into commercial manufacturing. This rolefocuses on cross-functional project coordination, technical transfer, GMPcompliance, and continuous process improvement. This is not a laboratoryrole, but a Life Sciences background is required to effectively collaboratewith 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.
  • ApplyLean 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, pleasesend us your updated resume at

hr@dawarconsulting.com

/

akansha@dawarconsulting.com

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