Team Lead Managed Access Program

• Bachelor’s degree in pharmacy or Life Sciences, Advanced degree (Master's/PhD) preferred. Additional certifications in Good Distribution Practice (GDP), Good Manufacturing Practice (GMP), or Pharmacovigilance is an advantage.
• Languages: Excellent knowledge of English language (spoken and written).
• 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, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

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!

• • Strong understanding of regulatory requirements related to MAP operations management.• Knowledge of GDP/GMP requirements and QA procedures.• Excellent communication skills with demonstrated ability to convey critical information professionally and collaborate with stakeholders and operations teams across multiple geographies.• Advanced skills in Excel, sound knowledge of Outlook, Word, and PowerPoint.• Strong project management, organization, and planning capabilities.• Ability to work independently under pressure and manage multiple stakeholders effectively.• Problem-solving skills and solution-oriented approach in complex matrix environments.• Knowledge of ICH Q7A Good Manufacturing Practice guidelines for active pharmaceutical ingredients and EU Directive requirements.• Understanding of pharmacovigilance inspection processes, including Individual Case Safety Reports (ICSRs), Periodic Safety Update Reports (PSURs), and regulatory compliance requirements.• Familiarity with clinical trial regulations, investigational medicinal product (IMP) management, and auxiliary medicinal product (AxMP) distribution.• Experience with quality management systems, audit preparation methodologies, and CAPA processes in a pharmaceutical environment.• Knowledge of cold chain custody requirements, temperature-controlled distribution, and security of pharmaceutical consignments.
• Proficient MS office skills. Service Now & PowerBI will be a plus.