? We’re Hiring | RA Executive

Location:
Delhi

Experience:
2–3 Years

Department:
Regulatory Affairs

GPC Medical Ltd. is looking for a
Regulatory Affairs (RA) Executive
to join our team. The ideal candidate should have hands-on experience in regulatory documentation, QMS, audits, risk management, and medical device registration.

Key Responsibilities
- Prepare, review, and implement
Quality Management System (QMS) procedures
.
- Prepare and maintain
Technical Files
for medical devices.
- Conduct and coordinate
Supplier Audits and Internal Audits
.
- Prepare and maintain
Risk Management, PMCF, CER, Product Descriptions
, and other regulatory documents.
- Prepare and review the
Master List of Documents, Master List of Records, Obsolete Document List, CAPA, Change Control
, and related QMS documentation.
- Assist in preparing
regulatory dossiers
for product registration in domestic and international markets.
- Ensure regulatory documentation is accurate, updated, and compliant with applicable requirements.




- Coordinate with internal teams to support regulatory submissions and compliance activities.

Candidate Profile:
- 2–3 years of relevant experience
in Regulatory Affairs, preferably in the
medical device/healthcare industry
.
- Graduate/Postgraduate in
Pharmacy, Life Sciences, Biotechnology, Medical Devices, or a related field
.
- Good understanding of
QMS, Technical Files, Risk Management, CER, PMCF, CAPA, and Change Control
.
- Knowledge of medical device regulatory requirements and registration processes.
- Strong documentation, analytical, and coordination skills.
- Valuable written and verbal communication skills.
- Strong attention to detail and ability to manage regulatory documentation within timelines.

Interested candidates can share their CV at [email protected] or click the apply button
Hiring #RegulatoryAffairs #RAExecutive #MedicalDevices #RegulatoryJobs #QMS #MedicalDeviceJobs #DelhiJobs #JobsInDelhi #HiringNow

📌 Executive - RA (New Delhi)
🏢 GPC Medical
📍 New Delhi