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

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

[email protected]/[email protected]