Company information Solvias is an internationally recognized provider of integrated solutions in contract analytical research, development and manufacturing. The company offers a broad spectrum of services and solutions in the Pharmaceutical, Biotech, Medical Device, Cell&Gene Therapy and Cosmetic industries. With headquarters near Basel, Switzerland, over 800 highly qualified employees take pride in putting science at the heart of serving customers to bring safer and better products to market faster.

Enable Excellence in Bioanalytics - Support Science with Smart Systems and Strong Standards

• Write and review quality documents, including validation protocols, reports, and SOPs
• Design, implement, and maintain Chromeleon templates (instrument methods, processing methods, and report templates) to support reliable and compliant chromatographic analyses
• Collaborate closely with Biological HPLC scientists and other team members, providing expert support and fostering a service-minded approach
• Contribute actively to the establishment and improvement of processes and workflows within the newly formed support team in the Biological HPLC unit

Your Profile

• Extensive experience in biopharmaceutical release and stability testing, with strong expertise in method validation and related regulatory requirements
• Good understanding of method validation requirements and experience in preparing and reviewing related quality documents
• Hands-on expertise in Chromeleon CDS, especially in creating and managing instrument methods, processing methods, and report templates
• Proactive and service-oriented mindset with excellent teamwork and communication skills
• Fluent in English and German is an advantage

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