Drug Regulatory Affairs Executive
2 days ago
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
-
Drug Regulatory Affairs
6 days ago
Delhi, Delhi, India Job Provider Baddi Full timeResponsibilities: - 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...
-
Drug Regulatory Affairs Officer
2 weeks ago
Dwarka, Delhi, Delhi, India Career Strategy Solutions Full timeUrgent Hiring Drug Regulatory Affairs for Pharmaceutical Company in Delhi. DRUG REGULATORY AFFAIRS (DRA) **Job Description**: Knowledge of Dossier Compilation as per the Country Guideline (CTD, ACTD, and Country Specific Format) Knowledge of COPP, FSC, Product Permission, and Summary of Product Characteristics Knowledge of Technical Documents like -...
-
Regulatory Affairs Executive Cdsco
4 days ago
Nehru Place, Delhi, Delhi, India PU Professional Utilities Pvt. Ltd Full timeWe 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...
-
Regulatory Affairs Cdsco Executive
4 days ago
Delhi, Delhi, India Professional Utilities Full timeWe 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...
-
Regulatory Affairs
2 weeks ago
Delhi, India First Choice Consultant Service Full timeProfile: Regulatory Affairs (CDSCO) Location: Paschim Vihar, New Delhi **Salary**: Up to 50,000 5 Days Working Exp: 1 to 2 Years Yearly Bonus Office Timing: 9:30 to 5:30 **Job Descriptions**: - Proficient in English. - Must understand the regulatory requirements for medical devices in India. - Significant experience within the legislative and...
-
Regulatory Affairs Specialist
7 days ago
Delhi, India Dr. Reddy's Laboratories Full timeJob Summary We are seeking a detail-oriented Specialist in Regulatory Affairs primarily focusing on Oligonucleotides typically has a role that involves ensuring compliance with regulatory requirements for these products. Responsibilities include managing chemistry, manufacturing, and controls (CMC) documentation for DMF submission, addressing deficiency...
-
Manager - Regulatory Affairs (RoW)
6 days ago
Delhi, Delhi, India Curiza LIfeciences Pvt. Ltd. Full time ₹ 60,00,000 - ₹ 1,00,00,000 per yearJob 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,...
-
Regulatory Affairs Pharmacist
4 days ago
Delhi, Delhi, India 2MG Inc. Full time ₹ 4,00,000 - ₹ 8,00,000 per yearWe'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...
-
New Delhi, India Dr. Reddy's Laboratories Full timeJob SummaryWe are seeking a detail-oriented Specialist in Regulatory Affairs primarily focusing on Oligonucleotides typically has a role that involves ensuring compliance with regulatory requirements for these products. Responsibilities include managing chemistry, manufacturing, and controls (CMC) documentation for DMF submission, addressing deficiency...
-
New Delhi, India Dr. Reddy's Laboratories Full timeJob SummaryWe are seeking a detail-oriented Specialist in Regulatory Affairs primarily focusing on Oligonucleotides typically has a role that involves ensuring compliance with regulatory requirements for these products. Responsibilities include managing chemistry, manufacturing, and controls (CMC) documentation for DMF submission, addressing deficiency...