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Technical Transfer Specialist

Full-time

Dawar Consulting - HR Service, Staffing Service, Consulting & Project Management in Fremont CA

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).

Continuous Improvement

  • 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 .

 

If interested, please send us your updated resume at

 

 

Vacancy posted a month ago
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