Regulatory Executive

Wrig Nanosystems; Solan; On-site; INR 600,000 - 900,000; Full time

Job summary

Wrig Nanosystems in Parwanoo, India, is seeking a Regulatory Executive with 2+ years' experience in Pharma/Medical Devices to join our team. You will manage regulatory submissions, prepare dossiers, and coordinate with CDSCO and state authorities.

The role requires knowledge of regulatory requirements, licenses, renewals, and cross-department coordination with QA, R&D, and production. Bachelor's or Master's in Pharmacy, Science, or MBA preferred.

Qualifications

• 2+ years of regulatory affairs experience.
• Experience with pharma or medical device regulatory requirements.
• Knowledge of CDSCO and State FDA processes.

Responsibilities

• Regulatory submissions, product registrations & renewals.
• Preparation and maintenance of regulatory dossiers & documentation.
• Coordination with CDSCO, State FDA and other regulatory authorities.
• Ensuring compliance with applicable regulatory requirements.
• Handling licenses, approvals, amendments and regulatory records.
• Coordination with QA, R&D, Production and other departments.
• Supporting regulatory audits and inspections.

Skills

Regulatory submissions

Dossiers preparation

Regulatory coordination

QA collaboration

Education

B.Pharm / M.Pharm / B.Sc. / M.Sc. / MBA

Tools

CDSCO liaison

Job description

Were Hiring | Regulatory Executive

We are looking for a Regulatory Executive to join our team in the Pharmaceutical / Medical Device industry.

Position: Regulatory Executive
Experience: 2+ Years
Industry: Pharma / Medical Devices
Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc. / MBA
Location: Parwanoo

Key Responsibilities:

• Regulatory submissions, product registrations & renewals
• Preparation and maintenance of regulatory dossiers & documentation
• Coordination with CDSCO, State FDA and other regulatory authorities
• Ensuring compliance with applicable regulatory requirements
• Handling licenses, approvals, amendments and regulatory records
• Coordination with QA, R&D, Production and other departments
• Supporting regulatory audits and inspections

Preferred: Candidates with relevant experience in Pharma or Medical Device manufacturing, particularly in Regulatory Affairs/Regulatory Compliance.