Hiring RA & QA Associates for a Renowned Healthcare Division at Delhi.

Job Description:

Position: RA & QA Associate 
Location: Delhi
Working Days: 5 Days | Monday - Friday  | Timings: 9:00 AM – 5:00 PM

Role Overview

Responsible for regulatory submissions, product registrations, license renewals, and compliance for medical devices in India and neighboring countries. Supports Quality Management System (QMS), audits, CAPA, supplier/distributor quality, and ensures compliant labeling, documentation, and distribution practices in line with medical device regulatory requirements.

Key Responsibilities:

• Prepare and manage regulatory submissions for medical device approvals, renewals, and change notifications.

• Monitor and interpret CDSCO, BIS, EPR, and other device-related regulations.

• Maintain licenses, certifications, and regulatory documentation.

• Support QMS implementation, internal/external audits, and CAPA processes.

• Review and approve medical device labels, artworks, and promotional content.

• Manage supplier/distributor quality and device complaint handling.

• Coordinate with consultants, government agencies, and internal teams.

Qualification & Experience

• Master’s in Pharmacy, Biotechnology, or Life Sciences.

• 2–5 years’ experience in RA & QA (Healthcare / Medical Device).

• Knowledge of Indian FDA, ISO 13485, and global regulatory norms.

Additional Details

• Contract: 1 Year (Renewable).

• Payroll: Talisman HR Solution.

• Benefits: PF, ESIC / Insurance, Annual Leaves.

• Future Scope: May be considered for on-roll role that is on Companies Payroll based on performance.

For more details, visit: https://www.talismanstaffing.com/our-clientele/

Contract period, auto-renewable or not: 1 year. Can be renewed with evaluation.
On Third Party Payroll (Talisman HR)

Interested can share updated cv on search@talismanstaffing.com or What's app : 9136435341