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Salary
≈ $90k – $222k per year (Estimated)
Location
In office (Cairo)
Seniority
Architect · 5+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 24, 2026. First seen by Alion on Oct 19, 2026. Sanofi scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Sanofi is a French pharmaceutical company formed in 1973 and assembled over five decades through a long series of mergers including Synthelabo, Aventis and Genzyme. It is now built around immunology and rare disease, with Dupixent for atopic dermatitis and asthma as by far its largest product, alongside a substantial vaccines division covering influenza, meningitis and the respiratory syncytial virus antibody Beyfortus. Headquartered in Paris, the group has sharpened its focus in recent years by separating its consumer healthcare business into the standalone company Opella and directing research spending toward biologics and immune science.

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

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

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