Pharma Lab Analyst – MS Method Dev & Particle ID

Eurofins; Eigenbrakel; Sur place; EUR 42 000 - 66 000; Plein temps

Avantages offerts par ce poste

Eco-Cheques €250/Year

12 ADV days

Team lunches

Résumé du poste

Eurofins PSS Insourcing Solutions is seeking a motivated lab analyst for our pharmaceutical analytical laboratory. The role focuses on identifying and investigating particles during stability studies and development projects, and involves developing and applying LC-MS and GC-MS methods.

You will contribute to method validation, stability testing, and reporting of findings to cross-functional teams. A master’s degree in chemistry or analytical chemistry and at least 2 years with LC-MS/GC-MS are

Qualifications

• Holds a master’s degree in chemistry or analytical chemistry.
• Initial experience in a pharmaceutical laboratory environment through a first professional position.
• Strong interest in scientific investigations and problem-solving.
• Has a minimum of 2 years of experience with LC-MS and/or GC-MS instrumentation.
• Experience in analytical method development and familiarity with analytical method validation principles.
• Experience working in a GMP environment is a plus.
• Outstanding written and communication skills in English.

Responsabilités

• Particle Identification and Material Characterization: Investigate particles and contaminants using structural and physicochemical techniques.
• LC-MS and GC-MS Method Development and Application: Develop and optimize LC-MS/GC-MS methods and support E&L and degradation product analysis.
• Analytical Method Validation: Plan and execute method validation studies and assess performance characteristics.
• Stability Testing: Prepare and analyze samples from stability studies and interpret results.

Connaissances

Problem-solving

Written communication

English proficiency

Formation

Master's degree in chemistry or analytical chemistry

Outils

LC-MS

GC-MS

Description du poste

Eurofins PSS Insourcing Solutions is seeking a motivated lab analyst for our pharmaceutical analytical laboratory. The role focuses on identifying and investigating particles during stability studies and development projects, and involves developing and applying LC-MS and GC-MS methods.

You will contribute to method validation, stability testing, and reporting of findings to cross-functional teams. A master’s degree in chemistry or analytical chemistry and at least 2 years with LC-MS/GC-MS are