Quality Control Analyst

We are seeking a motivated and detail-oriented Quality Control Manager to support laboratory quality activities and ensure that raw materials, in-process samples, and finished products meet established quality standards. This is a hands-on role focused on analytical testing, documentation review, deviation management, and compliance with GMP and internal quality procedures.

The successful candidate will work closely with Quality Assurance, Production, and other cross-functional teams to maintain product quality and support continuous improvement initiatives. This position does not include direct team leadership responsibilities.

Key Responsibilities

• Perform and/or coordinate routine quality control activities for raw materials, in-process samples, and finished products.
• Review analytical data, laboratory records, certificates of analysis, and batch-related documentation for accuracy and compliance.
• Ensure testing activities are carried out in accordance with GMP, SOPs, specifications, and applicable regulatory requirements.
• Support investigations related to out-of-specification (OOS) results, deviations, non-conformances, and laboratory incidents.
• Contribute to CAPA, change control, and continuous improvement activities within the Quality Control function.
• Maintain accurate laboratory documentation and ensure compliance with Good Documentation Practices (GDP).
• Support internal audits, customer audits, and regulatory inspections by providing QC documentation and technical input.
• Collaborate with Production, Quality Assurance, Engineering, and Supply Chain teams to resolve quality-related issues.
• Assist with method verification, equipment qualification activities, and implementation of new laboratory procedures where required.

Candidate Profile

• Bachelor’s degree or equivalent qualification in Chemistry, Pharmaceutical Sciences, Biology, Biotechnology, or a related scientific field.
• 2–4 years of experience in a Quality Control role within a GMP-regulated environment.
• Hands-on experience with analytical testing techniques such as HPLC, GC, UV-Vis, dissolution testing, microbiological testing, or similar methods.
• Good understanding of GMP, laboratory documentation requirements, and quality management systems.
• Experience supporting investigations, deviations, CAPA, and change control activities is advantageous.
• Strong attention to detail, organisational skills, and a structured approach to problem solving.
• Ability to work independently while collaborating effectively with cross-functional teams.
• Fluent French required, both written and spoken.