Scientist QC - Late Phase (a) - (fixed-term 12 months)

Scientist QC - Late Phase (a) - (fixed-term 12 months) # Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With a comprehensive service offering, Bachem provides pharmaceutical and biotechnology companies worldwide with products for research, clinical development, and commercial application. Headquartered in Switzerland with locations in Europe, the USA, and Asia, Bachem operates internationally and possesses more than 50 years of experience and industry-wide unique expertise. The company is listed on the SIX Swiss Exchange. Further information at: www.bachem.com To drive our continuous organic growth, we are constantly looking for highly qualified specialists. Become part of a dedicated team responsible for quality control in the late development phase with the highest demands for precision and reliability. To strengthen our team in QC Late Phase, we are looking for a dedicated Scientist Quality Control with a focus on GC, GC-MS & IC (a), 100% - (fixed-term 12 months) Your tasks: • You monitor analytical activities with a focus on GC, GC-MS & IC within the framework of release analyses, development projects, or analytical orders. In doing so, you are the contact person for technical questions from internal and external customers as well as authorities. Through sound technical assessment and secondary checks, you ensure that all results meet our high quality standards - scientifically sound, traceable, and precise. • You develop GC, GC-MS, and IC analytical methods and perform method validations and transfers according to regulatory requirements (cGMP). • In interdisciplinary project teams, you contribute your expertise and assume technical responsibility. You communicate clearly with internal interfaces such as QA, Production, or Regulatory Affairs, thereby contributing to quality along the entire value chain. • You adhere to all relevant instructions, regulations, and specifications to ensure the correctness of daily work in accordance with cGMP, occupational safety, and environmental protection, actively implement them, and serve as a role model for the team. • You assume responsibility for the processing and closure of Q-events (OOX-s, deviations). In doing so, you create and control QC data, documents, and process incidents as well as technical reports. • You check and create QC documents and consistently implement regulatory requirements (cGMP). Your forward-looking perspective allows you to recognize and establish compliance changes early on. • You are committed to the continuous further development and optimization of QC processes, systematically document technical findings, and strengthen a shared quality culture in the team through active knowledge exchange. Your profile: • Completed studies MSc / PhD in natural sciences (FH, Uni) • Professional experience in the pharmaceutical industry and in the GMP environment • Specialist knowledge in the analytical environment in handling chromatographic methods, GC, GC-MS & IC desirable • Knowledge of analytical method validation & transfers in the regulated GMP environment • Strong analytical thinking skills • Communicative and well-structured organizational talent • Convincing and confident appearance • Very good German and English skills in speaking and writing Our offer: • A dynamic and strongly growing work environment with internal development opportunities • Flexible working hours with the possibility of home office and the option to take additional vacation days with a reduced workload • Employee development through numerous internal and external training opportunities • 60% coverage of pension fund contributions by Bachem AG as well as the possibility for supra-mandatory provision with our elective savings plan • Access to the Swibeco benefits platform with discounts from external partners • Fresh, healthy, and diverse food in our staff restaurant • Diverse free sports activities on the Bachem Campus Have we aroused your interest? Then we look forward to receiving your complete application documents via our application portal. Learn more about the Bachem Group and let yourself be inspired by our inspiring work environment at our location in Bubendorf! At Bachem, you will find a diverse, multicultural team. (a) in the job title stands for everyone. We look forward to applications from all people. Skills and motivation count - completely independent of age or gender, origin, religion, or sexual orientation. *Note: Applications from recruitment agencies will not be considered.* Forward job advertisement via email