Scientist; GMP Analytics; f​/m​/d

Scientist(GMPAnalytics)(f/m/d)

Worklocaction:

Kaiseraugst|Workload:100%|Contracttime:temporary

Long-termtemporaryemploymentwiththeoptionofapermanentposition

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.

We are searching for Scientists to lead and execute analytical development, validation, and characterisation 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.

• Design, develop, optimise, and validate analytical methods (e.g., assay, impurities, product characterisation)
• Plan and execute feasibility studies, method development, and validation programmes
• 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 route‑n testing and continuous improvement initiatives where required

• Degree (B.Sc., M.Sc., or Ph.D.) in Analytical Chemistry, Pharmaceutical Sciences, Life Sciences, or 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 Characterisation: DLS, AUC
  • Mass Spectrometry (basic exposure desirable)
  • Compendial/Physicochemical Testing:
    Osmolality, CCI‑T (e.g., vacuum/pressure decay, headspace analysis), clarity/color, pH, other compendial (Ph. Eur./USP) tests
  • 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

• 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