Regulatory Affairs Executive Job at Wrig Nanosystems

Regulatory Affairs Executive Job at Wrig Nanosystems | Freshers Eligible

Mohit May 30, 2026

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Regulatory Affairs Executive Job at Wrig Nanosystems | Freshers Eligible

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Wrig Nanosystems Hiring Freshers for Regulatory Affairs Executive | Medical Devices

🏢 Wrig Nanosystems

📍 Parwanoo, Himachal Pradesh

📄 Regulatory Affairs Executive

🧑‍💻 0–2 Years

Wrig Nanosystems has announced an exciting opportunity for the position of Regulatory Affairs Executive at its facility in Parwanoo, Himachal Pradesh. This role is ideal for freshers and early-career professionals interested in Medical Device Regulatory Affairs, CDSCO compliance, ISO 13485 quality systems, and MDR documentation.

Candidates from Biomedical Engineering, Biotechnology, Life Sciences, Medical Devices, Pharmacy, Engineering, and related disciplines are encouraged to apply.

📋 Job Overview

Particulars	Details
Position	Regulatory Affairs Executive
Company	Wrig Nanosystems
Location	Parwanoo, Himachal Pradesh, India
Job Type	Full-Time
Experience	0–2 Years
Industry	Medical Devices / IVD
Work Mode	On-Site
Qualification	Bachelor's / Master's Degree

💰 Expected Salary Range: ₹3.0 LPA – ₹5.5 LPA

🏢 About Wrig Nanosystems

Wrig Nanosystems is focused on developing next-generation diagnostic technologies and innovative healthcare solutions in the Medical Devices and In-Vitro Diagnostics (IVD) sector.

The company works on advanced healthcare technologies while ensuring compliance with global regulatory standards and quality systems.

📌 Key Responsibilities

Support regulatory compliance activities related to CDSCO, MDR, IVDR, and international regulations.
Prepare and maintain technical documentation including DHF, DMF, PMF, and V&V reports.
Assist in ISO 13485 quality management system compliance.
Support risk management activities as per ISO 14971 requirements.
Maintain software validation documentation and traceability records.
Coordinate with Research & Development, Quality Assurance, and cross-functional teams.
Support regulatory submissions and documentation updates for Medical Devices and IVD products.

🎓 Required Qualifications

Biomedical Engineering
Biotechnology
Life Sciences
Medical Devices
Engineering
Pharmacy
Related Disciplines

Experience:

Freshers can apply.
Professionals with up to 2 years of experience are also eligible.

📚 Preferred Knowledge Areas

Medical Device & IVD Regulations
Regulatory Affairs Processes
CDSCO Regulations
European MDR & IVDR
ISO 13485 Quality Management Systems
ISO 14971 Risk Management
Technical Documentation Preparation
Software Validation
IEC 62304 (Preferred)

💡 Required Skills

Strong Documentation Skills
Analytical Thinking
Regulatory Compliance Understanding
Technical Writing Abilities
Cross-Functional Collaboration
Attention to Detail
Problem-Solving Skills

🎁 Why Join Wrig Nanosystems?

Opportunity to work in the growing Medical Device and Diagnostics industry.
Exposure to global regulatory standards and compliance frameworks.
Hands-on experience with CDSCO, MDR, IVDR, and ISO 13485.
Collaborative work environment with R&D and Quality teams.
Career growth opportunities in Regulatory Affairs and Quality Assurance.

📄 Resume & Interview Preparation Tips

Highlight Regulatory Affairs, Medical Devices, Quality Systems, and Documentation experience.
Mention knowledge of CDSCO, MDR, IVDR, ISO 13485, and ISO 14971 if applicable.
Keep your resume ATS-friendly and well-structured.
Showcase technical writing and documentation skills.