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Selvita Group in Kraków is seeking a Senior/Regular Analytical Chemist in Quality Control to ensure rigorous QC of pharmaceutical and bioanalytical products. You will work in an international, collaborative setting with state-of-the-art laboratories.
The role requires a life sciences degree, hands-on chromatography and spectrophotometric experience, and at least two years in a lab. Fluent English and strong planning skills are essential, with opportunities for professional development.
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.