Upstream Staff Scientist, Field Applications - MA

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Upstream Processing Field Applications Scientist How You Will Make an Impact At Thermo Fisher Scientific, our mission is to enable our customers to make the world healthier, cleaner, and safer. As an Upstream (USP) Field Application Scientist (FAS) within the Bioproduction Group, you will serve as a bioprocessing domain expert—helping biotechnology and biopharmaceutical customers accelerate technology adoption, process design, and optimization across upstream workflows. You will engage customers on a peer-to-peer, application-focused basis, providing technical leadership and process insight before, during, and after the sale. Acting as both a trusted advisor and problem solver, you will ensure customers achieve compliance, speed, and performance using Thermo Fisher Scientific solutions while helping shape our future innovations through Voice of Customer (VOC) feedback.

Serve as a technical expert and consultant, applying deep bioprocessing knowledge across upstream processing and single-use technologies. Engage customers peer-to-peer to support process development, optimization, and technology integration across upstream workflows. Lead pre- and post-sales technical activities, including product evaluations, proof-of-principle (PoP) studies, demos, pilot runs, and technology qualification in regulated environments. Provide comprehensive troubleshooting as the entry point for quality and performance issues, collaborating with Quality, Field Service, and Technical Support to ensure fast, compliant resolution. Deliver technical training for both internal and external audience-covering process scientists, engineers, and operators—to build capability and confidence in Thermo Fisher systems. Conduct workflow consulting and GEMBA walks at customer sites to identify process improvement opportunities and align solutions with operational goals. Support Bioprocessing Development Center (BDC) activities and on-site demonstrations, ensuring consistent messaging and technical excellence. Develop and implement adoption plans with measurable achievements (e.g., time-to-first-run, time-to-first-GMP lot) and conduct follow-up utilization reviews. Document all activities in CRM/SFDC, maintaining accurate technical engagement records, win plans, and risk mitigation plans. Collaborate cross-functionally with Account Managers, Field Service Engineers, Technical Support, Product Management, R&D, and Quality/Regulatory to deliver seamless end-to-end outcomes. Gather and communicate the Voice of Customer (VOC) to inform product roadmaps, feature development, and best-practice content (application notes, white papers, and case studies). Represent Thermo Fisher Scientific at industry events—including conferences, workshops, and webinars—by delivering workflow-based technical presentations and thought leadership. How You Will Get There Education BSc/MSc/PhD in Chemical Engineering, Biochemical Engineering, Bioengineering, Biotechnology, or a related discipline (or equivalent bioprocessing experience).

7+ years of hands-on experience in bioprocessing (Process Development, MSAT, or cGMP Manufacturing) with proficiency in at least one of the following: Single-use bioreactors (5–2,000 L+), cell culture, or perfusion systems Proven record of technical engagement and process troubleshooting in Process Development and/or cGMP environments. Experience supporting scale-up, tech transfer, and process optimization projects from development to manufacturing. Knowledge, Skills, and Abilities Deep understanding of bioprocessing workflows, cGMP principles, and regulatory expectations (FDA, EMA, Annex 1). Ability to interpret URS, P&IDs, batch records, and qualification protocols; comfortable with automation systems and process control HMIs. Skilled in process design, optimization, and workflow consulting, using data-driven analysis to