Regulatory Affairs Analyst

Radiant Systems Inc

Mumbai

On-site

INR 600,000 - 1,000,000

Full time

10 days ago

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Job summary

Radiant Systems Inc. in Mumbai seeks a detail-oriented Regulatory Affairs Analyst to support global regulatory processes and RIMS workflows.

You will help maintain documentation, ensure data integrity, and enable timely reporting across regions. The role collaborates with cross-functional teams, handles data validation in ETQ and SAP, develops Excel-based insights, and supports audits while aligning with Indian and global regulatory standards.

Qualifications

  • 1-3 years of experience in a regulated industry (medical device, pharmaceutical, cosmetics).
  • Proven ability to communicate effectively in written and spoken English.
  • Hands-on experience with ETQ, RIMS and document management systems.
  • Familiarity with Indian regulatory guidelines and global compliance standards.

Responsibilities

  • Manage global Registration, Notification, and Certification (RNC) processes in ETQ and other systems.
  • Generate and analyze SAP reports to support regulatory compliance and improvements.
  • Maintain master datasets in Excel and Power BI; support monthly reporting with GRA teams.
  • Validate data in EQT systems for accuracy and compliance.
  • Coordinate with global teams to ensure timely regulatory submissions and documentation.
  • Assist audits and maintain documentation in line with regulatory standards.
  • Drive continuous improvement for data integrity and reporting processes.
  • Provide expertise in regulatory documentation and RIMS workflows.
  • Support standardized system approaches aligned with industry best practices.

Skills

Attention to detail
Cross-functional collaboration
English communication
Time management
Problem solving

Education

Bachelor's degree in Sciences / Engineering / Regulatory Affairs / Life Sciences

Tools

ETQ
RIMS
SAP ERP
Power BI
Excel (VLOOKUP, Pivot Tables)
Document management systems

Job description

  • We are seeking a detail-oriented and collaborative Regulatory Affairs Analyst to support global regulatory processes and compliance initiatives. This role will contribute to the automation and maintenance of regulatory documentation within a RIMS workflow solution, ensuring data integrity and timely reporting across multiple geographic regions. The ideal candidate will be based in Mumbai and work closely with cross-functional teams, with flexibility to support global operations across time zones.
Key Responsibilities
  • Manage the global Registration, Notification, and Certification (RNC) process, including data entry, maintenance, and reporting in ETQ and other systems.
  • Generate and analyze SAP reports to ensure regulatory compliance; identify new stop codes using Excel functions like VLOOKUP.
  • Maintain and update master databases in Excel and Power BI; support monthly reporting and follow-ups with GRA teams.
  • Validate and monitor data in EQT systems for accuracy and compliance.
  • Collaborate with global teams to ensure timely regulatory submissions and documentation.
  • Support audits and maintain documentation aligned with regulatory standards.
  • Drive continuous improvement initiatives for data integrity and reporting processes.
  • Provide functional expertise in regulatory documentation and RIMS workflows.
  • Assist in maintaining standardized system approaches aligned with industry best practices.
Basic Qualifications
  • Bachelor’s degree in Sciences, Engineering, Regulatory Affairs, Pharmaceutical Sciences, Life Sciences, or a related discipline.
  • 1-3 years of experience in a regulated industry (e.g., medical device, pharmaceutical, cosmetic).
  • Proven ability to communicate effectively in written and spoken English.
Preferred Qualifications
  • 3+ years supporting a regulatory or compliance organization.
  • Experience in Regulatory Affairs or related field, particularly within a compliance function.
  • Hands‑on experience with ETQ, RIMS, and document management systems.
  • Familiarity with Indian regulatory guidelines and global compliance standards.
  • Advanced proficiency in Microsoft Excel (VLOOKUP, Pivot Tables) and exposure to Power BI.
  • Experience with SAP ERP systems and EQT or similar quality tracking tools.
  • Strong analytical, organizational, and leadership skills.
  • Demonstrated ability to work independently, manage multiple priorities, and meet deadlines.
  • Collaborative, responsive, and innovative problem solver with a global mindset.
  • Ability to work effectively in virtual teams across cultures and time zones.
Additional Skills
  • Ability to influence and engage across organizational levels.
  • Strong attention to detail and ability to retain confidential information.
  • Experience working in quality systems aligned with global regulations for Medical Devices, Consumer Products, and Cosmetics.
  • Technical aptitude to assess needs, identify issues, recommend solutions, and lead change initiatives.
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