Pharma QC Lab Analyst — HPLC Specialist

Nalys; Wallonië; Sur place; EUR 42 000 - 64 000; Plein temps

Résumé du poste

Nalys is seeking a Quality Control Laboratory Analyst to join the QC department of a major pharmaceutical organization in a large, structured team. The role focuses on analytical testing of intermediates, APIs, and finished products, with emphasis on HPLC and physico-chemical analysis.

The successful candidate will work within a collaborative environment, adhere to GMP standards, and contribute to data integrity and deviation investigations.

Qualifications

• Bachelor's degree in a scientific field required.
• Around 5 years of relevant experience for a medior profile; strong HPLC skills valued.
• Solid hands-on HPLC and physico-chemical analysis experience.
• Strong command of Empower software.
• GMP knowledge and ALCOA+ quality standards understood.
• Autonomous, proactive, and comfortable in a large team.
• Fluent in French with good English reading comprehension.
• GC/NMR experience or familiarity with LIMS/TopSpin is a plus.

Responsabilités

• Perform analytical testing on pharmaceutical products following established procedures.
• Prepare samples, reagents, and analytical equipment (HPLC, GC).
• Launch, monitor, and process analytical runs.
• Review analytical data and ensure specifications compliance.
• Contribute to deviation investigations and corrective actions.
• Document lab activities accurately (raw data recording).
• Participate in lab maintenance, calibration follow-up, and housekeeping.
• Organize work autonomously based on weekly planning.
• Join daily or regular team follow-up meetings.

Connaissances

HPLC

GMP awareness

Autonomy

French fluency

English reading proficiency

Formation

Bachelor's degree in a scientific field

Outils

Empower software

Description du poste

Nalys is seeking a Quality Control Laboratory Analyst to join the QC department of a major pharmaceutical organization in a large, structured team. The role focuses on analytical testing of intermediates, APIs, and finished products, with emphasis on HPLC and physico-chemical analysis.

The successful candidate will work within a collaborative environment, adhere to GMP standards, and contribute to data integrity and deviation investigations.