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Selvita, a global integrated service provider with laboratories in Krakow, Poznan and Wroclaw, seeks a Quality Control Specialist in the analytical chemistry team. You’ll contribute to drug discovery projects for biotech and pharma clients worldwide in a collaborative environment.
The role requires a life sciences degree, chromatography and spectrophotometric techniques, and MS experience, with at least two years in a lab, plus fluency in English and Polish.
Selvita is a global integrated service provider with laboratories in Poland (Krakow, Poznan, and Wroclaw), Croatia (Zagreb), and offices in Cambridge, UK, as well as the Greater Boston Area and San Francisco Bay Area in the US. Our company is dedicated to delivering comprehensive solutions that support our international clients in drug discovery and drug development.
As one of the largest preclinical contract research organizations in Europe, Selvita is driven by a clear mission: to bridge the gap between early drug discovery and the clinical stage of drug development.
At Selvita, we value partnership, excellence, passion, commitment, and integrity. We build strong, collaborative relationships with our clients and commit to the highest standards of quality. We fuel our pursuit of innovative solutions with enthusiasm, advance drug development with focused dedication, and ensure honesty and transparency in all our work.
As a Quality Control Specialist in analytical chemistry team, you’ll play a vital role in the Drug Discovery processes for biotech and pharma companies from Europe, USA and the rest of the world. You'll be working in a friendly and collaborative environment created by open-minded people, always ready for new challenges that new projects can bring, with an everyday opportunity to exchange knowledge with experienced members of the team. The variety of projects we run offers an opportunity to profile a career path in an interesting and diverse way.