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

Dawar Consulting, Inc.
Posted a month ago, valid for 17 days
Location

San Vicente, AZ, US

Salary

$32 per hour

Contract type

Contract

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Sonic Summary

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  • Our client, a leading biotechnology and gene therapy company, is hiring a Transfer Specialist for Reagent Manufacturing Operations in Tucson, AZ.
  • This long-term contract position offers a pay rate of $32 per hour on a W2 basis, along with benefits including medical, dental, vision, and a 401K plan.
  • The role requires a Bachelor's or Master's degree in Life Sciences and at least 1 year of experience in regulated industries such as pharmaceuticals or biotechnology.
  • Key responsibilities include coordinating product transfers, ensuring compliance with cGMP, and managing project documentation and milestones.
  • Candidates should possess strong communication and organizational skills, with familiarity in Lean principles being a plus.

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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