QA Manager

il y a 1 jour


Paris, France QA Temps plein

QA Manager (GCP/GCLP) - Specialty LabLocation – FranceRemote, Hybrid or Office-based (Paris)• Are you passionate about quality and compliance in a clinical laboratory setting?• Do you thrive in a role where you can shape quality processes and ensure regulatory excellence?• Looking for a high-impact opportunity within a growing clinical research organization?Vector is partnered with a global clinical research business in the central & specialty lab services space. We are seeking a Quality Assurance Manager – Specialty Lab to oversee quality operations and ensure regulatory compliance across specialty laboratory sites in France.This opportunity is ideal for an experienced QA professional eager to implement best practices, enhance quality systems, and drive continuous improvement in a fast-paced environment.International Scope – Work within a global research organisation supporting clinical trials worldwide.Autonomy & Impact – Lead quality initiatives across key laboratory sites, shaping processes and compliance frameworks.Career Growth – Gain exposure to global QA teams, diverse regulatory standards, and professional development opportunities.Dynamic Environment – Be part of an experienced team implementing new quality systems in a specialised lab setting.As a Quality Assurance Manager, you will play a crucial role in:Strengthening quality management systems across specialty labs.Driving internal audits, supplier quality management, and CAPA implementation.Supporting continuous improvement of QA processes and laboratory best practices.Collaborating with cross-functional teams, including QA, R&D, and project management.Key ResponsibilitiesEnsure compliance with GCLP, ISO 15189, GCP, and GLP standards.Oversee document control, procedural updates, and validation reports.Lead internal audits and support external regulatory inspections.Manage non-conformance investigations and implement CAPA actions.Monitor quality performance metrics and drive process enhancements.Develop and deliver QA training for laboratory staff.Work closely with cross-functional teams to align quality initiatives across sites.About YouYou are a solutions-driven QA professional with a strong background in laboratory operations and regulatory compliance. You thrive in a dynamic environment and are comfortable leading quality initiatives.QA experience in a laboratory or clinical research setting.Strong knowledge of GCLP, GCP, and GLP (ISO 15189/9001 is a plus).Fluent in French (English proficiency is an advantage).Experience in audit management, QMS, and supplier quality processes.Excellent problem-solving skills to drive continuous improvement.Strong communication and leadership abilities to collaborate across teams.Travel RequirementRegular travel within France is required – initially weekly, then reducing to every 2-3 weeks.If you are ready to take on a high-impact role in a leading clinical research environment, we’d love to hear from you Apply today to be part of a team dedicated to advancing clinical development and improving patient outcomes.Please note: if you are not contacted within 14 days of applying, you have not been successful in your application, and we appreciate your time taken to apply, and wish you the best of luck in your job search. #J-18808-Ljbffr



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