Reliability Engineering Intern

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 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! We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives. We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world. Discover more about us visiting www.sanofi.com or via our movie We are Sanofi Start a career that makes a difference. Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies. Whether it’s using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.