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Jr RA Executive

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Jr RA Executive

Arni Medica

Jr RA Executive

Skills

Testing & QARComplianceRegulatory Compliance

8 months ago

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Important information


Contract type:

Permanent

Location:

Sultanpur, Uttar Pradesh, India

Work mode:

Onsite

Published on:

13 October 2026

What they need


Job highlights

  • We are looking for motivated and detail-oriented fresh graduates to join our Regulatory Affairs (RA) team
  • Skills Required: .
  • Basic knowledge of medical device regulations and documentation . Understanding of ISO 13485 and regulatory compliance (preferred) . Strong attention to detail and documentation skills . Good communication and coordination abilities .

Job Summary

Arni Medica is a leading medical device manufacturer specializing in contract manufacturing, new product development, and high-quality production of nephrology and healthcare products. We are looking for motivated and detail-oriented fresh graduates to join our Regulatory Affairs (RA) team. This role offers exposure to medical device regulations, product registrations, technical documentation, and compliance processes.

Key Responsibilities

  • Assist in preparation and compilation of regulatory dossiers for medical devices.
  • Support product registration and licensing activities with regulatory authorities (CDSCO and other global markets).
  • Maintain and organize technical documentation, Device Master Files (DMF), and regulatory records.
  • Ensure compliance with applicable regulatory standards and guidelines.
  • Assist in Labelling review, IFU (Instructions for Use), and artwork compliance checks.
  • Support change control documentation and regulatory impact assessments.
  • Coordinate with QA, R&D, and production teams for regulatory submissions.
  • Track regulatory submissions, approvals, and renewals.
  • Assist in handling queries from regulatory bodies and auditors.
  • Maintain regulatory databases and ensure timely updates.

Qualifications & Skills

Education:

  • B.Pharm / M.Pharm OR B.Sc / M.Sc in Life Sciences, Biotechnology, Microbiology, Chemistry OR B.Tech / Diploma in Biomedical Engineering or related field

Skills Required:

  • Basic knowledge of medical device regulations and documentation
  • Understanding of ISO 13485 and regulatory compliance (preferred)
  • Strong attention to detail and documentation skills
  • Good communication and coordination abilities
  • Willingness to learn regulatory processes and global requirements

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