Technical Transfer Specialist - Manufacturing Operations

The Fountain Group is currently seeking a Transfer Specialist for a prominent client of ours. This position is located in Tucson, AZ. Job Description: Pay: $30‐32/hr Shift: 100% Onsite Duration: 12‑month 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 and 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 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. #J-18808-Ljbffr