Meril, a globally recognized medical device company, is hiring Officer / Executive / Assistant Manager – Regulatory Affairs for its Vapi, Gujarat facility. This is an excellent opportunity for professionals with medical device regulatory affairs experience who want to work on global regulatory submissions, technical documentation, and compliance in a fast-growing MedTech organization.
If you are looking for a Regulatory Affairs job in the medical device industry, this Meril opening offers strong career growth, exposure to international regulations, and hands-on involvement in innovative healthcare products.
🏢 Company Overview – Meril Life Sciences
Meril is a leading Indian medical device manufacturer with a global footprint, known for innovation, quality systems, and compliance with US FDA, EU MDR, ISO 13485, and other international standards.
📌 Job Details
- Position: Officer / Executive / Assistant Manager – Regulatory Affairs
- Location: Vapi, Gujarat, India
- Employment Type: Full-time, On-site
- Industry: Medical Devices
- Experience: Relevant Regulatory Affairs experience (Medical Devices preferred)
🔧 Key Responsibilities – Regulatory Affairs (Medical Devices)
- Lead and oversee end-to-end medical device testing aligned with international standards
- Ensure compliance with risk management frameworks and design control principles
- Prepare and review technical files, regulatory dossiers, and submission documents
- Manage and evaluate product data for global regulatory approvals
- Coordinate with Engineering, Product Management, Quality, and Marketing teams
- Support product development from a regulatory compliance perspective
- Maintain timelines and ensure documentation readiness for audits and submissions
🎓 Qualifications & Skills Required
- Degree in Pharmacy, Biomedical Engineering, Life Sciences, or related field
- Strong knowledge of medical device regulations and regulatory documentation
- Familiarity with ISO 13485, EU MDR, US FDA, and global regulatory requirements
- Excellent communication, documentation, and coordination skills
- Detail-oriented, proactive, and able to work in a fast-paced regulatory environment
💼 Salary & Benefits
- Estimated Salary: ₹4,50,000 – ₹9,00,000 per annum (based on role & experience)
- Opportunity to work on innovative medical technologies
- Exposure to global regulatory frameworks
- Strong learning culture and career growth opportunities
- Collaborative and professional work environment