Drug Regulatory Affairs Executive

4 hours ago


Nehru Place Delhi Delhi, India Trikuta Global Pvt LTD Full time ₹ 60,000 - ₹ 3,00,000 per year

Company Name: Professional Utilities

Website:

Job Title: Drug Regulatory Affairs Executive

Location: Nehru Place, New Delhi

Employment Type: Full-time

Company Overview

Professional Utilities Pvt Ltd is a leading business consulting firm helping startups and enterprises with compliance, licensing, and regulatory approvals. Our services include company incorporation, GST, trademark, FSSAI, drug license, CDSCO approvals, BIS, EPR, and other regulatory solutions. We aim to simplify complex compliance processes for businesses across India.

Job Overview

We are looking for a knowledgeable and detail-oriented Drug Regulatory Affairs Executive to manage drug license applications and CDSCO approvals for our clients. The role involves preparing documentation, coordinating with authorities, and ensuring compliance with applicable laws under the Drugs & Cosmetics Act, 1940. The ideal candidate should have strong knowledge of regulatory processes and excellent communication skills to handle client requirements efficiently.

Key Responsibilities

  • Prepare and file applications for drug licenses, wholesale/retail licenses, import/export licenses, and CDSCO approvals on behalf of clients.
  • Ensure compliance with the Drugs & Cosmetics Act, 1940, and related guidelines.
  • Guide clients regarding required documents, processes, and timelines.
  • Coordinate with regulatory bodies (CDSCO, State FDA, Pollution Control Boards, etc.) for approvals and clarifications.
  • Maintain accurate and up-to-date records of applications, approvals, and renewals.
  • Assist in responding to regulatory queries and audits.
  • Stay updated with changes in drug regulatory laws, CDSCO notifications, and related compliance requirements.
  • Collaborate with internal teams (Sales & Operations) to ensure smooth service delivery to clients.

Requirements

  • Bachelor's or master's degree in pharmacy, life sciences, or a related field.
  • 1–3 years of experience in drug regulatory affairs, licensing, or compliance.
  • Good understanding of CDSCO processes and drug licensing regulations.
  • Strong documentation and report-writing skills.
  • Excellent communication and client-handling skills (Hindi & English).
  • Ability to work under deadlines and manage multiple client projects.

How to apply:

Either send your resume on WhatsApp at or by mail at

Job Type: Full-time

Pay: From ₹25,000.00 per month

Work Location: In person



  • Delhi, Delhi, India OM Sai Management Consulting Services Full time

    Designation: - **Drug Regulatory Affairs-Male/Female** **JOB DESCRIPTION: -** - Delivery/Proper packing of goods for supplier - Maintaining the stock status at the back office - Settling of credit notes and following ups of payments from the parties - Coordinate with the vendors by keeping the track on purchase & delivery of orders sent - Maintaining the...


  • Delhi, Delhi, India Job Provider Baddi Full time

    Responsibilities: - Develop and implement regulatory strategies for drug development, registration, and commercialization in compliance with local and international regulations. - Coordinate regulatory submissions and responses to regulatory agencies, ensuring accuracy, completeness, and timeliness. - Maintain up-to-date knowledge of regulatory...


  • Nehru Place, Delhi, Delhi, India PU Professional Utilities Pvt. Ltd Full time

    We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...


  • Delhi, Delhi, India Professional Utilities Full time

    We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...


  • Delhi, Delhi, India Curiza LIfeciences Pvt. Ltd. Full time ₹ 60,00,000 - ₹ 1,00,00,000 per year

    Job Role: International Regulatory AffairsResponsible for compilation & submission of Dossier of a generic drug.Hand on experience in Filing dossiers to regulated, emerging and ROW markets.Experienced in CTD/ACTD and Regional Module.Experience in Filing in EU, ASEAN, MIDDLE EAST AND LATAM regions.To obtain approvals for relevant product marketing,...


  • Delhi, India Oswal Crop Protection Pvt. Ltd. Full time

    Company Description Oswal Crop Protection Pvt. Ltd. is an ISO 9001:2015 certified company, established by Mr. Ramesh Bansal, who has over 30 years of experience in the pesticides industry. As one of the leading agrochemical companies in India, Oswal Crop Protection is committed to strengthening agriculture with sustainable products and services. Our...


  • Delhi, India Savvi Sales & Services Full time

    Job Title: Regulatory Affairs Executive Location: Rohini, Delhi Industry: Pharmaceuticals / Nutraceuticals Salary Package: 25,000 50,000 per month Gender Preference: Male Experience Required: 2–3 years in Pharma or Nutra Industry (Regulatory Affairs) Key Responsibilities: Prepare and submit regulatory dossiers such as INDs, NDAs, ANDAs, MAAs. Ensure proper...


  • Delhi, Delhi, India 2MG Inc. Full time ₹ 4,00,000 - ₹ 8,00,000 per year

    We're Hiring – Regulatory Affairs Pharmacist | New Delhi Do you want to join a company that is on track to become the No. 1 Oncology & Hematology company in the Philippines next year? If yes, this is your chance.At GetMeds, we believe in more than just medicines. We believe in partnerships, innovation, and building a legacy of accessible, life-saving...


  • Delhi, Delhi, India Ace Cathtech Pvt. Ltd. Full time ₹ 6,00,000 - ₹ 9,00,000 per year

    Company DescriptionAce Cathtech Pvt Ltd, established in April 2024, is a cutting-edge manufacturer of premium medical devices, specializing in Nephrology Products, Cardiac Surgery Equipment, Critical Care, and Anesthesia Products. Located in Faridabad, Haryana, our state-of-the-art facility adheres to the highest manufacturing standards, including a Class 7...


  • New Delhi, India Fusion Technology Solutions Full time

    The main role of a Drug Safety Associate is to monitor the safety of drugs and medical devices once they are on the market and ensure that they are being used safely. - Reviewing and evaluating adverse event reports (AERs) to determine if they meet regulatory reporting requirements. - Entering and maintaining adverse event information in safety databases -...