Arni Medica
Jr RA Executive
Skills
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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