Senior QC Lab Technician – GMP & Data Integrity

Ekkiden; Longeau; Sur place; EUR 42 000 - 62 000; Plein temps

Avantages offerts par ce poste

Comprehensive health insurance (GEREP)

Meal vouchers (Swile card)

Résumé du poste

Ekkiden is seeking a QC laboratory technician to strengthen quality control activities in a GMP environment. You will perform analyses on raw materials, intermediates and finished products, ensuring procedures and data integrity are followed.

You will bring 5–10 years in a pharmaceutical QC lab, with GMP experience, GLP knowledge, and strong teamwork. The role offers growth and a collaborative environment at our site and adjacent functions.

Qualifications

• Quality control in GMP environment.
• GLP knowledge required.
• Data integrity awareness.
• Experience in managing OOS/OOT results.
• Strong teamwork and communication.

Responsabilités

• Perform quality control analyses in compliance with GMP and internal procedures.
• Carry out physicochemical analyses on pharmaceutical samples.
• Perform or participate in microbiological analyses according to laboratory needs.
• Prepare samples, solutions, reagents and media required for analyses.
• Use and maintain laboratory equipment.
• Participate in investigations for atypical or out of specification results (OOS / OOT).
• Document analysis results in quality systems and files.
• Ensure traceability and data integrity per GMP requirements.
• Participate in qualification, calibration and maintenance of laboratory equipment.
• Draft and update laboratory documents and procedures.
• Collaborate with QC, QA, production and engineering teams.

Connaissances

Quality control

GLP

Data integrity

OOS/OOT

Teamwork

Formation

CFC laborantin(e) or equivalent (chemistry/biology/pharmacy)

Description du poste

Ekkiden is seeking a QC laboratory technician to strengthen quality control activities in a GMP environment. You will perform analyses on raw materials, intermediates and finished products, ensuring procedures and data integrity are followed.

You will bring 5–10 years in a pharmaceutical QC lab, with GMP experience, GLP knowledge, and strong teamwork. The role offers growth and a collaborative environment at our site and adjacent functions.