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Technical Transfer Specialist

Job in Tucson, Pima County, Arizona, 85718, USA
Listing for: Dawar Consulting
Full Time position
Listed on 2026-06-18
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 32 USD Hourly USD 32.00 HOUR
Job Description & How to Apply Below

Technical Transfer Specialist

Tucson, United States | Posted on 04/30/2026

Our client, a world leader in diagnostics and life sciences, is looking for a Technical Transfer Specialist based out of Tucson, AZ.

Job Duration: Long term Contract (Possibility Of Further Extension)

Pay Rate: $32/hr on W2

DOE

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

We are seeking a Technical Transfer Specialist to support the transfer of new assays, reagents, and diagnostic products from R&D into manufacturing. This role ensures smooth product integration with a focus on manufacturability, quality, compliance, and scalability
. The ideal candidate will have experience in GMP environments
, strong coordination skills, and a foundation in process improvement and technical documentation
.

Key Responsibilities Technical Transfer
  • Support product and process transfer from development to manufacturing.
  • Coordinate cross‑functional activities with R&D, Operations, Quality, and Regulatory teams.
  • Track project milestones and ensure timely execution of transfer activities.
  • Document manufacturing processes, scalability considerations, and best practices.
  • Assist with process validation readiness and troubleshooting during transfers.
Quality & Compliance
  • Ensure adherence to cGMP, SOPs, and regulatory standards
    .
  • Support audit readiness and documentation for compliance activities.
  • Assist in investigations, deviations, and corrective actions (CAPA/NCR).
  • Apply Lean principles and problem‑solving tools (e.g., 5 Whys, Fishbone).
  • Analyze process data using tools like Minitab to improve efficiency and reduce risk.
  • Develop and maintain standardized procedures and documentation.
Required Qualifications
  • Bachelor’s or Master’s degree in Life Sciences (Biology, Chemistry, Biochemistry, etc.) or Engineering (Biomedical/Chemical).
  • 1+ year of relevant experience in biotech, pharma, or medical device industry.
  • Experience working in a GMP/regulated environment
    .
  • Strong understanding of SOPs, documentation, and quality compliance
    .
  • Excellent communication, teamwork, and project coordination skills.
Preferred Qualifications
  • Exposure to technical transfer, manufacturing, or process development
    .
  • Knowledge of Lean / Six Sigma methodologies
    .
  • Familiarity with assay, reagent, or diagnostic product manufacturing
    .
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