Quality Assurance & Regulatory Affairs Specialist – Dental / Medical Devices

Meerut, Uttar Pradesh

Golden Bird Healthcare is a growing manufacturer and exporter of dental materials, committed to innovation, quality, and global regulatory compliance.

Role Overview

We are looking for a Quality Assurance & Regulatory Affairs Specialist to manage regulatory documentation, ensure compliance with applicable standards, and support product registrations for dental and medical devices.

Key Responsibilities

- Prepare and maintain regulatory documentation and technical files
- Ensure compliance with CE,CDSCO, ISO standards, and applicable regulatory requirements
- Manage regulatory submissions and product registrations
- Monitor regulatory updates and ensure company compliance
- Liaise with regulatory authorities and certification bodies

Qualifications

- Bachelor’s or Master’s degree in Life Sciences, Chemistry, Pharmacy, or related field




- Experience in Regulatory Affairs / Regulatory Compliance
- Knowledge of medical device or pharmaceutical regulations
- Strong documentation, analytical, and communication skills
- Ability to work independently and in a team setting

Location

Meerut, Uttar Pradesh (On-site)

Interested candidates may apply or send their resume to [email protected]

Job Type: Full-time

Pay: ₹20,000.00 - ₹35,000.00 per month

Benefits:

- Leave encashment
- Provident Fund

Application Question(s):

- Are you ready with Service Commitment / Bond Policy for 1 year or Alternative Option (No Bond) but total deducted amount will be refunded in full after successful completion of 12 months of service. ( deduct 10% of Salary per month )

Work Location: In person

📌 Quality Assurance & Regulatory Affairs Specialist – Dental / Medical Devices (Meerut)
🏢 Golden Bird Healthcare
📍 Meerut