R&D
Where your curiosity drives the
miracles of
science

Location: Stockholm, Sweden

Job type: Fixed-term (14 months), Full Time | Hybrid Work Policy

About the Job:

As Pharmacovigilance and Medical Information Officer within our Swedish and North Europe MCO team, you'll be a vital guardian of patient safety—monitoring, reporting, and communicating critical safety information while delivering high-quality medical information guidance to healthcare professionals and patients. Ready to get started?

You'll work at the heart of our commitment to patient safety, handling adverse event reports, managing safety surveillance activities, and responding to medical inquiries. This position combines hands-on Pharmacovigilance and Medical Information activities with active collaboration across the North Europe cluster. Your work directly contributes to the safe and effective use of our medicines in diabetes, transplant, immunology, and other therapeutic areas—helping us deliver on our promise to improve patient outcomes at scale. You'll be at the intersection of regulatory compliance, patient safety, and medical excellence, playing a key role in ensuring that every safety decision upholds Sanofi’s commitment to transforming lives through breakthrough medicines.

About Sanofi:

We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system—and innovative pipeline—enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

Main Responsibilities:

• Monitor and report adverse events according to local legislation and company quality standards, ensuring timely and accurate communication to Health Authorities and stakeholders

• Provide expert medical information support to healthcare professionals, patients, and internal teams, delivering high-quality responses to complex medical inquiries

• Support local safety surveillance activities, including risk management, product alerts, and market research programs in collaboration with the Country Safety Head

• Maintain comprehensive knowledge of pharmacovigilance regulations, medical information procedures, and the safety profiles of our product portfolio

• Collaborate with third-party partners and internal teams across the North Europe cluster to ensure seamless PV and MI operations

• Contribute actively to team projects and continuous improvement initiatives within the North Europe Pharmacovigilance and Medical Information team

• Ensure compliance with all regulatory requirements and company quality documents related to patient safety and medical information

About You:

• Experience: Background in the pharmaceutical industry, pharmacy practice, or related healthcare settings, ideally with exposure to pharmacovigilance or medical information activities

• Core Competencies: Strong planning and organizational skills with meticulous attention to detail; ability to work accurately under regulatory and compliance requirements; proven ability to manage multiple priorities effectively

• Communication Skills: Excellent written and verbal communication abilities; comfortable interacting with healthcare professionals, patients, and cross-functional colleagues; strong interpersonal skills with a collaborative mindset

• Technical Skills: Proficient with MS Office and relevant software systems; comfortable learning and working with pharmacovigilance databases and tools

• Languages: Fluent in English and Swedish (written and spoken)

• Education: University degree in Pharmacy, Medicine, or equivalent field

Why Choose Us?

• Protect patient safety by playing a critical role in monitoring and communicating the safety of medicines used by millions

• Make a global impact while working locally across the North Europe region in diabetes, transplant, immunology, and specialty care

• Collaborate across borders with diverse teams of safety experts, medical professionals, and regulatory specialists

• Develop specialized expertise in pharmacovigilance and medical information—highly valued skills in the pharmaceutical industry

• Grow your career in a streamlined, AI-powered organization that values smart, modern ways of working

• Contribute to innovation that improves patient outcomes, relieves pressure on healthcare systems, and expands access worldwide

• Join an inclusive workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice

#LI-EUR

null

Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com

Final compensation will be determined based on factors such as experience, skills, expertise, location, and others. Employees may be eligible to participate in company employee benefit programs.