Technical Transfer Specialist - Manufacturing Operations

The Fountain Group is currently seeking a­­­­­­­­Transfer Specialist for a prominent client of ours.  This position is located in ­­Tucson, AZ. Details for the position are as follows:

Job Description:

Pay: $30-$32/hr

Shift: 100% Onsite

Duration: 12-months to start – potential to extend or convert based on performance and budget.

Overview:

• Technical Transfer (70%)
  • Execute product design transfer tasks from late-stage development through commercial launch.
  • Coordinate process transfers from R&D to manufacturing sites (local or external) and track project milestones.
  • Collaborate cross-functionally with Operations, Development, Regulatory, and Project teams to align on manufacturability, quality, and cost objectives.
  • Document and integrate end-to-end manufacturing requirements and best practices, including scalability considerations, into transfer projects.
  • Utilize project management methodologies to execute transfer activities, troubleshoot issues, and support the evaluation of new tools and technologies.
  • Support process validation readiness by gathering necessary documentation and collaborating with Validation Engineers.
  • Actively participate in training and mentorship to develop technical excellence within the design transfer team.
• Quality, Safety, and Compliance (15%)
  • Ensure all processes are conducted safely and adhere strictly to current Good Manufacturing Practices (cGMP), local, international, and Roche (MQMS) standards.
  • Assist in audit readiness by collecting and organizing documentation, and supporting non-compliance events (e.g., Client investigations and corrective actions).
  • Keep updated with relevant regulations to maintain company compliance.
• Continuous Improvement (15%)
  • Learn and apply basic Lean principles and problem-solving methodologies (e.g., Five Whys, Fishbone diagrams) to identify and eliminate process inefficiencies.
  • Use statistical tools and software (e.g., Minitab) to analyze process data, minimize risk, and generate actionable plans for improvements.
  • Develop and maintain standardized procedures and documentation for processes.

Qualifications:

Bachelor’s degree in Engineering or Life Sciences required.

1+ year of relevant experience required.

cGMP experience is highly desired.  

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