Regulated Document Management Specialist (Life Sciences/Tobacco

About the role

Choosing Capgemini means choosing a place where you'll be empowered to shape your career, supported by a collaborative global community, and inspired to reimagine what's possible.

What you'll do

• Work closely with Quality, Regulatory, Manufacturing, R&D, and Compliance teams to ensure documentation accuracy, traceability
• Manage controlled documents including SOPs, work instructions, job aids, forms, specifications, and quality records from creation through retirement
• Administer document lifecycle activities including workflow management, metadata maintenance, version control, effective-date management, retention, archival
• Perform quality reviews to ensure document completeness, consistency, traceability, approved templates, and compliance with regulatory requirements
• Support Quality Management System (QMS) documentation processes and maintain repository accuracy

What you need

• 2–5 yrs of experience
• Microbiology
• Documentation
• ISO 9001
• SOP writing
• Reconciliation
• B.Sc