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Thermo Fisher is seeking a Field Application Specialist in the Netherlands. In this role, you will provide scientific expertise to support customers in LC-MS and HPLC solutions, with a focus on pharmaceutical and biopharmaceutical applications.
The successful candidate will have a master's degree or PhD and at least 3 years of hands-on experience in relevant instrumentation. Responsibilities include delivering training, supporting method development, and collaborating closely with various teams to ensure customer success.
As part of the Thermo Fisher Scientific team, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges.
The Chromatography and Mass Spectrometry business develops and manufactures innovative instruments, consumables, and software solutions for customers working in analytical sciences and scientific research. We play a critical role in supporting pharmaceutical and biopharmaceutical organizations through advanced LC-MS technologies, workflow optimization, and scientific expertise.
The Field Application Specialist (FAS) will provide advanced scientific and technical expertise to customers, sales teams, and internal partners within CMD (Chromatography and Mass Spectrometry Division), supporting LC-MS and HPLC solutions with a strong focus on Pharma and Biopharma applications.
The successful candidate will combine strong technical expertise in LC-MS and HPLC instrumentation with direct hands‑on experience in pharmaceutical and biopharmaceutical analytical workflows, including method development, troubleshooting, characterization, and operation within regulated laboratory environments. The role also requires a solid understanding of operational processes within structured pharmaceutical and biopharmaceutical organizations, including quality standards, compliance expectations, and cross‑functional collaboration.