At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
The LIMS Master Data Specialist is responsible for the creation, modification, maintenance, and verification of LIMS master data objects within LabWare. Working within the governance framework defined by the master data governance council, the Specialist handles requests from operational
OneStream Senior developer- OneStream / System Configuration / Business Rules (C# / VB.Net / ETL / SQL / IVD / Modern Integration Methods / English Project : For our customer a big pharmaceutical company in Kaiseraugst
Lab Technician (GMP Analytics) (f/m/d) Work locaction: Kaiseraugst | Workload: 100% | Contract time: temporary Long-term temporary employment with the option of a permanent position Who we are Solvias is an internationally recognized provider of integrated solutions for contract research. With its headquarters in Kaiseraugst near Basel, more than 500 highly qualified employees are proud to place science at the heart of customer service, helping to bring safe and high‑quality products to market faster At Solvias, we serve the world’s leading pharmaceutical innovators. That offers you the opportunity to make a meaningful impact on the health of patients worldwide, working with brilliant scientists in a fast-moving environment filled with stimulating challenges. Description of your role We are searching laboratory technicians to support analytical testing across multiple scientific teams (e.g., biologics, small molecules, parenterals, advanced therapies). This role offers the opportunity to work with a wide range of analytical techniques and to be deployed flexibly based on business needs and development opportunities. Your tasks Execute analytical testing in a GMP-regulated laboratory environment Perform sample preparation, measurement, data evaluation, and documentation Ensure accurate and compliant data recording in LIMS and laboratory systems Support analytical development and quality control of new therapies (e.g., biologics, small molecules, parenterals, advanced therapies) Take responsibility for laboratory equipment (operation, maintenance, troubleshooting) Collaborate with scientists and peers across different analytical domains Our requirements Laboratory technician (EFZ/CTA/BTA) or equivalent scientific training First experience in a GMP or regulated environment is an advantage Experience with one or more of the following analytical techniques preferably under GMP Chromatography: HPLC, UPLC, SEC / AF4-MALS Capillary Electrophoresis: CE-SDS, cIEF, CZE Spectroscopy: UV/Vis, Fluorescence, IR, CD, nanoDSC Particle & Imaging Techniques: Light obscuration, micro-flow imaging (MFI), optical microscopy, SEM/EDX Biophysical / Molecular Characterization: DLS, AUC Mass Spectrometry (basic exposure desirable) Compendial / Physicochemical Testing: Osmolality, CCIT (e.g., vacuum/pressure decay, headspace analysis), clarity/color, pH or other compendial (Ph. Eur./USP) tests Fluent in English, German is a plus Structured, reliable, and detail-oriented execution Ability to work independently while collaborating in teams High level of ownership and accountability Willingness to learn and adapt to new technologies and domains What we offer Fair and market‑competitive compensation Opportunity for a permanent position, depending on mutual fit and business development State‑of‑the‑art infrastructure at a modern work location Excellent staff restaurant offering high quality meals at fair prices Flat hierarchies and a collaborative and international working environment *Please note that, as part of this recruitment process, we cooperate with an external provider....
The Chromeleon Method Template Specialist is responsible for the translation, modification, maintenance, and verification of Chromeleon methods and report templates during the upgrade from Chromeleon 7.2.10 to 7.3.2. This position is limited for 1 year. Method
Scientist (GMP Analytics) (f/m/d) Work locaction: Kaiseraugst | Workload: 100% | Contract time: temporary Long-term temporary employment with the option of a permanent position Who we are Solvias is an internationally recognized provider of integrated solutions for contract research. With its headquarters in Kaiseraugst near Basel, more than 500 highly qualified employees are proud to place science at the heart of customer service, helping to bring safe and high‑quality products to market faster At Solvias, we serve the world’s leading pharmaceutical innovators. That offers you the opportunity to make a meaningful impact on the health of patients worldwide, working with brilliant scientists in a fast-moving environment filled with stimulating challenges. Description of your role We are searching for Scientists to lead and execute analytical development, validation, and characterization activities across multiple scientific domains (e.g., biologics, small molecules, parenterals, advanced therapies). The role combines scientific expertise, project ownership, and customer interaction, with flexible deployment across different analytical areas. Your tasks Design, develop, optimize, and validate analytical methods (e.g., assay, impurities, product characterization) Plan and execute feasibility studies, method development, and validation programs Interpret analytical data and derive scientific conclusions to support projects and customers Prepare and review technical documentation (protocols, reports, SOPs) in a GMP environment Present results and scientific insights to internal stakeholders and customers if necessary Lead or contribute to technical discussions and project execution Troubleshoot analytical methods and ensure robustness and compliance Collaborate cross-functionally with laboratory teams and support knowledge transfer Support routine testing and continuous improvement initiatives where required Our requirements Degree (B.Sc., M.Sc., or Ph.D.) in Analytical Chemistry, Pharmaceutical Sciences, Life Sciences, or a related field Relevant experience in analytical development, validation, and GMP-regulated environments is preferred In-depth experience with one or more of the following analytical techniques preferably under GMP Chromatography: HPLC, UPLC, SEC / AF4-MALS Capillary Electrophoresis: CE-SDS, cIEF, CZE Spectroscopy: UV/Vis, Fluorescence, IR, CD, nanoDSC Particle & Imaging Techniques: Light obscuration, micro-flow imaging (MFI), optical microscopy, SEM/EDX Biophysical / Molecular Characterization: DLS, AUC Mass Spectrometry (basic exposure desirable) Compendial / Physicochemical Testing: Osmolality, CCIT (e.g., vacuum/pressure decay, headspace analysis), clarity/color, pH or other compendial (Ph. Eur./USP) tests Particle & Imaging Techniques: light obscuration, MFI, microscopy, SEM/EDX Experience in method development, validation, and troubleshooting under GMP Strong understanding of data integrity and regulatory expectations Fluent in English, German is a plus Strong scientific mindset with ability to interpret complex data High level of ownership and accountability for deliverables Ability to work independently and manage multiple priorities Structured, detail-oriented, and compliant way of working Collaborative team player with strong communication skills Customer-oriented with ability to present complex topics clearly What we offer Fair and market‑competitive compensation