Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients
Reliability Engineering Intern
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.
About the Job
Reliability & Compliance Engineer Intern will be trained and exposed in the following responsibilities:
1. Equipment Requalification
- Plan, coordinate, and execute periodic equipment requalification activities (e.g., IQ/OQ/PQ as applicable).
- Review and update requalification protocols and reports to ensure compliance with GMP requirements.
- Liaise with Engineering, Production, and Validation teams to schedule requalification activities.
- Ensure calibration and validation status of equipment remains current and properly documented.
- Track requalification timelines and maintain requalification master schedules.
2. SOP Management & Updates
- Review and update Standard Operating Procedures (SOPs) to ensure alignment with current processes, regulatory requirements, and operational practices.
- Initiate document change requests (DCR) in accordance with the Quality Management System (QMS).
- Ensure proper version control, document approval workflows, and archival.
- Collaborate with cross-functional stakeholders to ensure SOP clarity and compliance.
- Support periodic document reviews to ensure documentation remains effective and compliant.
3. Compliance & Documentation
- Ensure activities comply with GMP and relevant regulatory standards.
- Support internal and external audits by preparing documentation and responding to audit queries.
- Assist in deviation investigations and CAPA implementation related to equipment or documentation gaps.
4. Annual Facility Review
- Conduct and document annual facility reviews to ensure compliance with GMP and regulatory requirements.
- Assess facility conditions, utilities, and environmental controls.
- Identify gaps and coordinate corrective actions where necessary.
- Ensure findings are documented and presented to management.
5. Annual Pest Control Review
- Review and assess annual pest control reports and monitor trends.
- Ensure pest control activities comply with site procedures and regulatory expectations.
- Liaise with pest control vendors to address findings or improvement areas.
- Maintain documentation for audit readiness
About You
Degree or Diploma preferably in a related field
Candidates from Polytechnic or University programmes are welcome to apply
Strong organizational and time management skills with the ability to manage multiple tasks simultaneously
Excellent written and verbal communication skills
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.
Find out more about this location
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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