GMP Laboratory Analyst (Temporary)

Job Description:

• Verifying analytical chemical tests within a GMP environment, including sample preparation, analysis, and reporting of results.
• Managing and maintaining HPLC equipment, including calibration, troubleshooting, and documentation of maintenance activities.
• Drafting validation protocols and reporting analytical methods according to GMP guidelines.
• Assisting in the preparation and maintenance of the Validation Master Plan (VMP) and performing Computer System Validation (CSV) activities.
• Collaborating with other departments to ensure all analytical activities comply with quality and safety standards.
• Contributing to the continuous improvement of laboratory processes and procedures.

Requirements:

• At least a master's degree in analytical chemistry or a related field.
• Proven experience within a GMP laboratory.
• Experience with HPLC management, including calibration and maintenance, preferably also in DQ, IQ, OQ, and PQ.
• Experience with Validation Master Plan (VMP) and/or Computer System Validation (CSV) is a plus.
• Excellent command of Dutch/French as well as English. Preferably good trilingual skills.
• Strong organizational and problem-solving skills.
• Ability to work both independently and as part of a team.