QC Validation & Compliance Section Head

Sanofi is a global healthcare company with a focus on innovative solutions for patients. While specific industry details are not provided, the presence of roles such as Medical Manager Immunology and Egypt Diabetes Medical Manager suggests involvement in therapeutic areas like immunology and diabetes management. These positions likely support clinical research, patient care, or medical education initiatives within Sanofi's broader healthcare ecosystem. The company may engage in pharmaceutical development, medical device innovation, or health services tailored to specific geographic regions or disease states. As a leader in the healthcare sector, Sanofi is positioned to drive advancements in treatment and care delivery through specialized medical leadership roles. Its operations likely span multiple countries, with a focus on addressing unmet medical needs through research, education, and patient support programs.

About The Job As QC Validation & Compliance Section Head, you will lead the team that keeps our Quality Control laboratories compliant, qualified and audit-ready. You will oversee method, process and cleaning validation, equipment qualification and calibration, and laboratory self-inspection programs. You will also coach and develop your team, so that every analysis supports the safe, reliable supply of medicines to patients. Main responsibilities Oversee process, method and cleaning validation activities, making sure protocols and reports meet quality standards and deadlines Supervise analytical method validation, analytical transfers and the implementation of validation plans Manage the annual qualification and calibration plan for laboratory equipment, including a semi-annual review of how well it is working Lead preventive maintenance and technical compliance for laboratory data systems, including user access and audit requirements Run monthly quality and safety self-inspections across the labs and report findings to the QC Manager Support quality-related investment planning, including technical specifications, supplier comparisons and equipment ordering and receipt Lead and develop the validation team, setting annual priorities and individual development plans, and train new analysts on good laboratory and documentation practices About You Bachelor's degree in Pharmaceutical Science or a related science field 5+ years of relevant experience in quality control validation or compliance, ideally within a multinational company Solid knowledge of GMP and GLP quality practices Strong leadership, organization and planning skills, with a sense of urgency Clear communication and interpersonal skills, and good command of English Good computer skills and familiarity with modern instrumental analysis techniques Show more