Manager Drug Regulatory Affairs (Domestic Market)

Randstad India; Ludhiana; On-site; INR 8,00,000 - 15,00,000; Full time

Job summary

A leading pharmaceutical recruitment firm is seeking an experienced Drug Regulatory Affairs professional in Ludhiana, Punjab. This full-time role involves managing regulatory submissions and ensuring compliance with Indian regulations. The ideal candidate has an M-Pharma degree and 10-18 years of experience, with expertise in CDSCO regulations. Join a supportive environment dedicated to innovation and patient well-being.

Benefits

Competitive pay

Growth path

Skill enhancement

Engaging work

Team spirit

Meaningful tasks

Qualifications

• 10-18 years of experience in Drug Regulatory Affairs.

Responsibilities

• Preparing and submitting regulatory dossiers to CDSCO and other relevant authorities.
• Ensuring compliance with domestic market regulations for all product lifecycle stages.
• Interacting with regulatory agencies and responding to queries.
• Monitoring regulatory changes and implementing necessary updates.
• Providing regulatory guidance to cross-functional teams.
• Contributing to the strategic planning of regulatory affairs.

Skills

Expertise in CDSCO regulations

Excellent communication skills

Proactive and detail-oriented approach

Education

M-Pharma degree or equivalent

Job description

Overview

Drug Regulatory Affairs (Domestic Market) – Ludhiana, Punjab, India

We are seeking an experienced and dedicated Drug Regulatory Affairs professional to join our dynamic team. This is a full-time position focused on managing domestic market regulatory submissions and ensuring compliance with all relevant Indian regulations. As a Drug Regulatory Affairs specialist, you will play a critical role in bringing life-saving and life-enhancing products to market efficiently and safely.

What do we offer you?

• Competitive pay
• Growth path
• Skill enhancement
• Engaging work
• Team spirit
• Meaningful tasks

Who are you?

• M-Pharma degree or equivalent
• 10-18 years of experience in Drug Regulatory Affairs
• Expertise in CDSCO regulations
• Excellent communication skills
• Proactive and detail-oriented approach

What are you going to do?

• Preparing and submitting regulatory dossiers to CDSCO and other relevant authorities.
• Ensuring compliance with domestic market regulations for all product lifecycle stages.
• Interacting with regulatory agencies and responding to queries.
• Monitoring regulatory changes and implementing necessary updates.
• Providing regulatory guidance to cross-functional teams.
• Contributing to the strategic planning of regulatory affairs.

Where are you going to work?

You will be working with a leading pharmaceutical company dedicated to innovation and patient well-being. Our client is committed to fostering a supportive and collaborative work environment. As a Drug Regulatory Affairs specialist, you will be an integral part of our client\'s success.

If you are a seasoned Drug Regulatory Affairs professional looking for a challenging and rewarding role, we want to hear from you. Apply now to become our next Drug Regulatory Affairs expert!