The Biosynth® Group is an innovative life science reagents, contract synthesis and manufacturing services company headquartered in Staad, Switzerland. We work as scientists for scientists and secure supply chains with consistent quality around the world. As a reliable supplier, manufacturer and partner to the pharmaceutical, life science and diagnostics industries as well as the food, agrochemical and cosmetics industries, we have facilities on three continents and a fast global distribution network. Our main production laboratories are located in Switzerland, the UK, Slovakia and China, peptide and antibody production in the USA and the Netherlands. Enzyme projects are located in Austria and biological IVD reagents in Ireland.
At the Berlin site, Biosynth GmbH carries out contract development and production in the field of bioconjugation and polymer-based drug delivery. Biosynth GmbH has a manufacturing license according to Section 13 AMG for the production of bioconjugated active ingredients and conjugate vaccines.

ESSENTIAL CANDIDATE REQUIREMENTS

• Understanding /experience of quality processes and procedures
• Proven organizational skills with the ability to prioritize one’s workload
• Experience in effective and cooperative team collaboration
• Fluent in written and spoken English and German
• Able to work independently and seek advice if necessary
• Strong IT skills, including word processing, spreadsheets, databases, and use of email and the Internet
• Excellent communicator (written and verbal)
• Great attention to detail

DESIRABLE CANDIDATE REQUIREMENTS

• A degree in a relevant scientific subject
• Relevant experience in a quality-relevant environment
• Experience in a pharma company or a CDMO
• Experience of working in a GMP environment
• Knowledge of an eDMS
• Knowledge of SAP

PURPOSE OF THE ROLE

The position holder will be a member of the quality assurance team and will be responsible for the areas of work aimed at executing and maintaining quality processes at the Berlin location