Technology Transfer Scientist

This is an exciting opportunity to join a global company in the medical in‑vitro diagnostics industry. As our organization experiences continued growth, we are seeking Tech Transfer Support to facilitate the introduction of new products (Thermo Controls) across our diverse range of testing technologies. The individual will be responsible for assisting with the execution and implementation activities for the launch of these new products and processes.

The individual will report to the Tech Transfer Manager and work under the guidance of a Senior Tech Transfer Scientist to help ensure that key project milestones are met.

• Operate within established Change Management, Verification, and Validation procedures to ensure compliance and maintain high‑quality standards. Contribute to the creation and maintenance of operations documentation, including FMEAs, validation plans, protocols, reports, SOPs, and related materials.
• Implement new and improved processes for Quality Operations Value Assignment teams, including integrating updates to software tools enhancing efficiency and accuracy.
• Assess product designs for alignment with Operations requirements, providing feedback to design teams to mitigate risks early to drive optimization of business and operational processes.
• Collaborate closely with R&D and technical partners to ensure thorough knowledge transfer, enabling smooth transition from development to Operations. Lead and/or support training initiatives to ensure teams are equipped with the knowledge and skills required for new processes, tools, or product introductions.
• Support overall program execution by helping teams meet key milestones and ensuring alignment with project timelines by coordinating activities across cross‑functional groups, proactively identify and resolve issues to maintain project momentum.

• Minimum of 3 years of experience in an Tech Transfer, Operational or Product Development/Support role within a GMP manufacturing environment.
• Demonstrated ability to successfully deliver project timelines.
• Track record of contributing to cross‑functional teams within a regulated environment.
• Knowledge of R&D and Operations (manufacturing, quality processes and systems) is required.
• Ability to recommend efficient solutions to harmonize potential process changes with operational preferences.
• Efficient use of common applications, such as MS Excel, is required.
• cGMP and external audit experience (GMED, FDA, etc.) is strongly preferred.
• Maintains an organized approach – understands priorities and escalates issues appropriately.
• Knowledge of the company’s products and quality system is preferred.
• Multi‑disciplined validation experience is strongly preferred (Process, Product, Method).
• Experience with Lean Manufacturing, Six Sigma and Mistake Proofing is preferred.