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Technical Transfer Specialist

Job Description

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
 

hr@dawarconsulting.com/kavitha@dawarconsulting.com