Quality Assurance Analyst
vor 3 Wochen
Relocation assistance may be available for eligible candidates and their families. This company is a global leader in the life sciences sector, active across multiple continents. While we operate at the forefront of scientific innovation, our true strength lies in the people who work together to develop ideas that help other organizations improve lives. We believe in giving employees ownership of their careers, and we value contributions of every size—because meaningful ideas shape the future. We want you to be part of that journey. This group processes all analytical samples from production around the clock. The team prepares, aliquots, and analyzes samples with precision, ensuring timely and reliable results that support a wide range of technologies. From chromatography and biochemical assays to microbiological and physicochemical methods, our team covers it all. Why This Role Stands Out As an Analyst in the QC 24/7 Analytical Services group, you can either focus on a specialized technology or develop broad expertise across many analytical platforms, such as: Bioburden and endotoxin testing Chromatographic techniques (e.g., HPLC, SEC) ELISA, UV measurements, TOC, pH, and more You’ll work in a fast-paced, technology-rich environment where no two samples are the same—an ideal setting for those who enjoy continuous learning and hands‑on science. What We Offer Close support from experienced colleagues during onboarding to help you gain any missing skills or knowledge Relocation support for qualified candidates and their families Opportunities for professional development and career growth, including training certifications for specific technologies A 4‑shift schedule offering unique weekday free time—perfect for enjoying quiet ski slopes or mountain trails in the region Primary Responsibilities Aseptically aliquot production samples Perform and document time‑sensitive in‑process control analyses (e.g., bioburden, endotoxin, HPLC, TOC, UV, pH) Carry out all activities in strict compliance with GMP guidelines Handle highly potent substances (AHSK 4/5) Your Profile Completed vocational training, ideally in a scientific or technical field such as biotechnology, pharmaceutical technology, chemistry, or process engineering GMP experience is an advantage Strong willingness to learn, adapt, and take initiative Careful, safety-conscious, and detail‑oriented working style Solid technical understanding and problem‑solving mindset Fluency in German; English skills are beneficial Willingness to work in a rotating 4‑shift system Please note: This job posting is just a preview of the full scope of the position. A comprehensive job description is shared by a member of our team. Seniority level Mid‑Senior level Employment type Full‑time Job function Analyst and Science Health and Human Services #J-18808-Ljbffr
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Quality Control Analyst
vor 3 Wochen
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