Technicien laboratoire contrôle qualité GMP (H/F/X)

The role:

As part of the strengthening of quality control activities within a pharmaceutical company, you will work as a QC laboratory technician in an environment subject to GMP requirements. You will carry out the analyses required to control raw materials, intermediate products and/or finished products, while ensuring compliance with procedures and regulatory requirements.

Responsibilities:

• 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 in case of atypical or out of specification results (OOS / OOT)
• Document analysis results in quality systems and files
• Ensure traceability and data integrity in accordance with GMP / data integrity requirements
• Participate in qualification, calibration and maintenance activities of laboratory equipment
• Draft and/or update laboratory documents and procedures
• Collaborate with QC, QA, production and engineering teams

What we are looking for:

• Degree such as CFC laborantin(e), bachelor's/master's in chemistry, biology, microbiology, pharmacy or equivalent qualification
• Minimum 5 to 10 years of experience in a pharmaceutical QC laboratory 
• Significant experience in a GMP environment
• Good command of good laboratory practices (GLP)
• Knowledge of data integrity requirements
• Experience in managing OOS/OOT results
• German at operational/intermediate level (french is a plus)
• Rigorous, autonomous and quality oriented profile
• Ability to work in a regulated and documented environment
• Good team spirit and good communication skills

Comment se déroule le processus de recrutement chez Ekkiden ?

Chez Ekkiden, nous nous engageons à offrir une expérience positive à chaque candidat.