QC Analyst

JobScope The QC Analyst is responsible for performing physicochemical, microbiological, and biological analyses of raw materials, in-process products, finished products, and packaging materials to ensure the quality and compliance of biosimilar products with GMP and regulatory requirements. The role supports laboratory operations through accurate testing, proper documentation, equipment management, and adherence to data integrity standards. Job Requirements

Education:
Bachelor’s degree to master’s degree (Bac +3 to Bac +5) in: Pharmacy, Biotechnology, Analytical Chemistry, Pharmaceutical Sciences, Laboratory Sciences

Experience:
1to 3 years of experience in a pharmaceutical laboratory
• Knowledge of GMP / GxP environments
• Experience in biotechnology or biosimilar products is considered an advantage Languages
• Fluent in French
• Basic technical knowledge of English (protocols, SOPs, reports) Professional Knowledge
• Knowledge of pharmaceutical analytical techniques (HPLC, UV, GC, ELISA, microbiological testing)
• Ability to read, interpret, and analyze analytical results
• Good understanding of GMP standards and laboratory documentation practices
• Basic knowledge of analytical method validation principles MainCompetencies
• High level of rigor and attention to detail
• Strong respect for procedures and laboratory discipline
• Good analytical and organizational skills
• Ability to work effectively within a team and under supervision
• Commitment to quality and compliance standards Dutiesand Responsibilities
• Perform analytical tests according to SOPs and validated methods (HPLC, GC, UV, ELISA, microbiological testing, etc.).
• Verify and review analytical results against established specifications.
• Conduct routine analyses and support quality investigations when required.
• Ensure strict compliance with GMP requirements during laboratory activities.
• Accurately complete laboratory records, analytical reports, and documentation.
• Ensure data integrity in compliance with ALCOA+ principles and Good Laboratory Practices.
• Prepare, calibrate, and maintain laboratory instruments and equipment.
• Report any equipment malfunction or maintenance requirement.
• Participate in instrument qualification activities (IQ/OQ/PQ).
• Identify and report Out of Specification (OOS) and Out of Trend (OOT) results.
• Support investigations under the supervision of the QC Supervisor.
• Contribute to Corrective and Preventive Actions (CAPA).
• Participate in analytical method transfer activities.
• Contribute to the optimization of QC methods and laboratory procedures.
• Support internal audits and external inspections under supervision.