Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients
Junior Quality Business Partner Greece & Cyprus
At a glance
Our teams produce and deliver over 4 billion units of medicines and vaccines every year, ensuring every breakthrough gets to the people who need it most.
Our state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation are redefining what’s possible: ensuring treatments reach patients faster, safer, and more sustainably than ever before. This is where your skills, ambition, and passion can shape the future of healthcare.
Job title: Junior Quality Business Partner Greece & Cyprus
- Location: Greece
- Hiring Manager: Anastasia Christopoulou
- Job Type: Fixed term (1 year), full-time
About the job
As Quality Business Partner for Greece & Cyprus within our Quality team, you'll play a crucial role in ensuring product quality excellence across both markets. This position combines technical quality expertise with strategic oversight, working closely with local and global teams to maintain the highest quality standards for Sanofi products. The ideal candidate will leverage their knowledge of GMP/GDP regulations and quality systems to drive continuous improvement while ensuring compliance with local and international requirements. Ready to chase the miracles of science?
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:
- Management of Product Quality Complaints (PTC) for Sanofi products marketed in Greece and Cyprus
- Management of Product Quality Review for products marketed in Greece and Cyprus
- Perform trainings to Sanofi employees and service providers personnel according to Sanofi procedures and regulatory requirements
- Review and approve quality-related documentation including SOPs
- Support the update of Quality Agreements with manufacturing sites
- Support the quality oversight on product distribution in Greece and Cyprus
- Support investigation of quality events, customer complaints, and implementation of corrective and preventive actions (CAPAs)
- Contribute to the operational execution of action plans related to management of changes with an impact on GxP or health-regulated processes.
- Support the maintenance of Quality Management Systems (QMS) in alignment with GMP, GDP, and local regulatory requirements
About you
Experience:
- 1-3 years of experience in pharmaceutical quality assurance, manufacturing, or regulatory affairs
Soft and Technical Skills:
- Strong analytical and problem-solving abilities
- Proficiency in Microsoft Office Suite
- Excellent written and verbal communication skills
- Understanding of quality systems and regulatory compliance frameworks
- Experience with Veeva Systems is an advantage
- Collaborative mindset: Ability to work effectively in cross-functional teams and build strong partnerships across the organization
- Detail-oriented: Meticulous attention to detail while maintaining focus on broader quality objectives
- Adaptability: Flexibility to manage multiple priorities in a fast-paced, evolving pharmaceutical environment
- Continuous learner: Enthusiasm for professional development and staying current with industry regulations and best practices
Languages:
- Fluency in Greek and English (written and spoken)
Why choose us?
- Join a leading pharmaceutical company and contribute to improving health outcomes worldwide.
- Be part of a company at the forefront of medical research and breakthrough therapies.
- Thrive in an environment that values diversity of thought and background.
- Shape market access strategies that directly impact the availability of life-changing treatments.
- Work closely with global and local teams, gaining exposure to various aspects of the pharmaceutical business.
- Become a go-to resource for understanding complex healthcare systems and payer landscapes in your region.
#LI-EUR
nullPursue 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
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Why work with us
- We’re problem-solvers and pioneers. United by the belief that everyone deserves a healthier future. We create best-in-class vaccines that prevent disease and protect lives.
- Innovation drives us. From AI and mRNA to next-gen science, we push the boundaries to deliver first- and best-in-class vaccines for infectious diseases worldwide.
- Growth happens here. With bold investments in R&D and world-class facilities, Sanofians across the entire vaccine lifecycle are shaping the future of global health.
- We do what’s right. Sustainability and DE&I drive our positive global impact—because the diverse communities Sanofians represent are the patients we serve.
All-in on diversity
At Sanofi, diverse perspectives fuel the best solutions for patients. Hear from Monique Vessey, our Supply Chain Transformation Leader, on how her background shapes her approach to delivering life-changing medicines.
"Manufacturing and Supply is the bridge between the science that happens in research laboratories and the people and communities we serve."
Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
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