Associate Regulatory Affairs Specialist – Radiant Systems

Are you passionate about regulatory compliance and global documentation management in the pharmaceutical or medical device industry?
Radiant Systems Inc is hiring an Associate Regulatory Affairs Specialist in Mumbai for a hybrid contract role. This position is ideal for science or pharma graduates with 1–3 years of experience who are eager to support global regulatory submissions and data management initiatives.

This opportunity allows professionals to contribute to automation-driven regulatory workflows, collaborate across global teams, and ensure compliance with international standards — all while growing in a dynamic and technology-driven environment.

🧩 Key Responsibilities

• Manage global Registration, Notification, and Certification (RNC) processes using ETQ and RIMS systems.
• Generate and analyze SAP reports to ensure compliance; identify new stop codes using Excel (VLOOKUP, Pivot Tables).
• Maintain master databases in Excel and Power BI for monthly reporting and compliance tracking.
• Validate regulatory data in EQT systems for accuracy and integrity.
• Support regulatory submissions, documentation, and audit readiness.
• Collaborate with global GRA teams to meet submission timelines.
• Drive continuous improvement initiatives for regulatory data processes.
• Assist in maintaining standardized regulatory workflows aligned with industry best practices.

🎓 Qualifications

Basic Requirements:

• Bachelor’s degree in Pharmaceutical Sciences, Life Sciences, Engineering, or Regulatory Affairs.
• 1–3 years of experience in a regulated industry (pharmaceutical, medical device, or cosmetic).
• Excellent written and verbal English communication skills.

Preferred:

• 3+ years of experience in Regulatory Affairs or Compliance.
• Hands-on with ETQ, RIMS, SAP ERP, or equivalent systems.
• Advanced Excel and Power BI skills.
• Knowledge of Indian and global regulatory standards.
• Strong analytical and multitasking abilities with attention to detail.

💼 Benefits

• Hybrid work model (2–3 days onsite for collaboration and training).
• Exposure to global regulatory operations and cross-functional teams.
• Skill development in advanced data management systems (ETQ, SAP, Power BI).
• Opportunity to grow within a reputed global organization.

📝 How to Apply

Application Link