Lab Analyst (LC-MS)

Eurofins PSS Insourcing Solutions; Brussel; Sur place; EUR 52 000 - 68 000; Plein temps

Avantages offerts par ce poste

Eco-Cheques

ADV days

Payflip access

Team lunches

Résumé du poste

Eurofins PSS Insourcing Solutions is seeking a motivated lab analyst to join its pharmaceutical analytical lab in Belgium. The role involves identifying particles and contaminants, developing LC-MS/GC-MS methods, and validating analytical methods within a GMP environment. English communication is required; French is a plus.

The position is a full-time, on-site role in Belgium with diverse team activities. Responsibilities include material characterization, data interpretation, and reporting to

Qualifications

• Master’s degree in chemistry or analytical chemistry.
• 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.

Responsabilités

• Investigate particles, fibers, polymeric materials and contaminants; document findings.
• Develop, optimize, and apply LC-MS and GC-MS methods for extractables, leachables, degradation products and unknowns.
• Participate in validation studies and evaluate method performance: specificity, accuracy, precision, linearity, robustness.
• Perform stability-related sample preparation, analysis, and result interpretation.

Connaissances

LC-MS instrumentation

GC-MS instrumentation

Analytical method development

Analytical method validation

GMP experience

English communication

Formation

Master's degree in chemistry or analytical chemistry

Outils

FTIR

Raman spectroscopy

SEM/EDS

Description du poste

Eurofins PSS Insourcing Solutions® is a global, award-winning insourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client' site, utilising their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility. If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions® is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries!

Job Description

We are seeking a motivated lab analyst to join our pharmaceutical analytical laboratory. The successful candidate will contribute to the identification and investigation of visible and subvisible particles encountered during stability studies, quality investigations, and development projects. The role also includes involvement in the development, validation, and application of LC-MS and GC-MS analytical methods. This position offers a unique opportunity to build expertise at the intersection of material characterization, mass spectrometry, and pharmaceutical stability testing. Main responsibilities include:

Particle Identification and Material Characterization

• Conduct investigations of particles, fibers, polymeric materials, and other potential contaminants.
• Utilize structural and physicochemical characterization techniques such as optical microscopy, FTIR, Raman spectroscopy, SEM/EDS, or equivalent techniques.
• Interpret analytical data to determine the likely origin and nature of unknown particles.
• Prepare technical reports and communicate findings to project, quality, and cross-functional teams.

LC-MS and GC-MS Method Development and Application

• Develop, optimize, and execute analytical methods using liquid chromatography-mass spectrometry (LC-MS) and gas chromatography-mass spectrometry (GC-MS).
• Support structural elucidation and identification of extractables and leachables (E&L), degradation products, and unknown compounds.
• Perform routine analyses as well as complex investigations requiring interpretation of mass spectral data.
• Contribute to instrument maintenance, troubleshooting, and qualification activities.

Analytical Method Validation

• Participate in the planning and execution of analytical method validation studies.
• Assess method performance characteristics including specificity, accuracy, precision, linearity, robustness, solution stability, and range.
• Previous experience with analytical method validation is considered an advantage but is not required.

Stability Testing

• Prepare and analyse samples generated from stability study programs.
• Review and interpret analytical results.
• Support investigations related to atypical, out-of-trend, or unexpected stability results.

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.
• Full communication skills (both written and verbal) in English. French is a plus.

Additional Information

• A full-time (40hours/week) Monday – Friday job.
• A Permanent contract with flexible working hours. (Can start between 7am and 9:30am)
• Place of work: Braine l'alleud, Belgium.
• Work in a fast growing international organization.
• Eco-Cheques +/- 250 Euro/Year.
• Additional 12 ADV days.
• A company well-being program targeting both mental and physical well-being.
• Access to Payflip, an innovative app that helps you take control and optimize your paycheck.
• A fantastic team with monthly team lunches, fun teambuilding activities (laser tag, escape rooms, sports, etc.) and above all; a great collaborative international work environment
• Personal development through learning on the job and additional trainings.