Scientist (GMP Analytics) (fmd)

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 highquality products to market faster.

At Solvias we serve the worlds 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 (. . 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 marketcompetitive compensation
• Opportunity for a permanent position depending on mutual fit and business development
• Stateoftheart 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.