Scientist (GMP Analytics)

Solvias; Kaiseraugst; Vor Ort; CHF 120.000 - 160.000; Vollzeit

Benefits dieser Stelle

Excellent staff restaurant

Flat hierarchies

International working environment

Zusammenfassung

Solvias seeks scientists to lead analytical development, validation, and characterization across biologics, small molecules, and parenterals. The role combines scientific expertise with project ownership and customer interaction, with flexible deployment across analytical areas.

Responsibilities include method development, validation, data interpretation, and preparation of GMP documentation. Collaboration with lab teams and knowledge transfer will be essential.

Qualifikationen

• Degree in Analytical Chemistry, Pharmaceutical Sciences, Life Sciences, or related field.
• Experience in analytical development, validation, and GMP environments is preferred.
• Experience with chromatography and biophysical/particle characterization techniques under GMP.

Aufgaben

• Design, develop, optimize, and validate analytical methods (assay, impurities, product characterization).
• Plan feasibility studies, method development, and validation programs.
• Interpret analytical data and derive scientific conclusions for projects and customers.

Kenntnisse

Analytical Chemistry

GMP knowledge

Data interpretation

Cross-functional collaboration

Ausbildung

B.Sc.

M.Sc.

Ph.D.

Tools

HPLC

UPLC

SEC / AF4-MALS

CE-SDS

cIEF

DLS

AUC

Jobbeschreibung

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.

• 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
• Particle & Imaging Techniques: Light obscuration, micro-flow imaging (MFI), optical microscopy, SEM/EDX
• Biophysical / Molecular Characterization: DLS, AUC
• Compendial / Physicochemical Testing: Osmolality, CCIT (e.g., vacuum/pressure decay, headspace analysis), clarity/color, pH or 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

What we offer

• Fair and market‑competitive compensation
• Opportunity for a permanent position, depending on mutual fit and business development
• 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.