Teamleader Method-Development and Validation (m/w) 100%

SGS is the world’s leading Testing, Inspection and Certification company. We operate a network of over 2,500 laboratories and business facilities across 115 countries , supported by a team of 99,500 dedicated professionals . With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, compliance and sustainability. Our brand promise – when you need to be sure – underscores our commitment to trust, integrity and reliability, enabling businesses to thrive with confidence. SGS Analytics Switzerland AG (formerly SYNLAB Analytics & Services Switzerland AG) offers a unique range of bioanalytical services for clinical development and drug development of pharmaceuticals and biologics. We provide a broad spectrum of analytical methods for PK analytics, immunogenicity, as well as for release and stability testing according to highest quality standards (GMP, GLP, GCP, ISO 17025). For more details, please follow this link and find more about our broad portfolio.

Laboratory management incl. supervisor function Responsible for managing and organizing the method development and validation activities of bioanalytical assays (HPLC-MS/MS, ligand-binding based and immunogenicity assays) Laboratory management including responsibility for management of laboratory personnel Design, develop, and validate bioanalytical assays utilizing HPLC-MS/MS, MSD and ELISA platforms Optimize assay conditions and identify, address, and resolve technical issues during assay development and validation to ensure reproducible and reliable results Conduct bioanalytical method validation and qualification in accordance with regulatory guidelines to support pre-clinical and clinical studies Review of documentation/raw data and approval of results, writing of standard operating procedure Prepare detailed reports documenting assay performance, validation, and data analysis Ensure scientific and experimental quality as a primary contact for our clients Application of electronic systems like eQMS and LIMS

Successfully completed studies in biochemistry, chemistry or comparable natural science Proven experience in leading teams and managing complex analytical projects Several years of experience in analytical development and validation within a GLP-regulated environment (HPLC-MS/MS, ligand-binding based and immunogenicity assays) Strong understanding of regulatory guidelines Experience in Chromatographic/MS-MS software packages and LIMS systems (e.g. Watson LIMS) Ability to work collaboratively and flexible in a results driven, team-oriented environment with a strong customer focus Independent, exact and efficient mode of operations with an analytical mindset and a solution-oriented approach Excellent communication skills, both written and verbal in English and German Interested in a broad and challenging spectrum of tasks and motivated to grow business Team player Willingness to take responsibility Good organizational and communication skills Accurate and timely organization and execution of all project work with consistent high quality Very good communication skills Exemplary organization of laboratory work Management of lab personnel