GMP Analytics Scientist: Method Development & Validation

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

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.