Transfer Specialist - Reagent Manufacturing Operations; GMP, Life Sciences/Pharma/Biotech
Job in
Tucson, Pima County, Arizona, 85718, USA
Listed on 2026-10-05
Listing for:
dawarconsulting
Full Time
position Listed on 2026-10-05
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Job Description & How to Apply Below
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
- 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.
- 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.
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