Career Opportunity: Regulatory Affairs Walk-in Drive at MSN Laboratories
MSN Laboratories, a prominent research-driven pharmaceutical company, is hosting a walk-in drive for experienced professionals in its Regulatory Affairs (FML Division). This presents an excellent opportunity for qualified individuals to join as Executive, Senior Executive, or Junior Manager at the company’s R&D Center located in Pashamylaram, Hyderabad.
About the Company:
As one of India’s leading pharmaceutical innovators, MSN Laboratories is dedicated to the development and manufacturing of high-quality Active Pharmaceutical Ingredients (APIs), finished dosage formulations, and specialty medicines. With state-of-the-art R&D facilities, global regulatory approvals, and an international market presence, the company is deeply committed to innovation, quality, and delivering affordable healthcare solutions worldwide.
Job Overview and Eligibility:
We are seeking enthusiastic B.Pharm and M.Pharm graduates with 2 to 7 years of hands-on experience specifically in Finished Manufacturing Line (FML) Regulatory Affairs. Successful candidates will play a crucial role in ensuring regulatory compliance for both domestic and international markets. The primary work location for these positions will be Pashamylaram, Hyderabad.
Key Responsibilities:
Responsibilities include the meticulous collection and preparation of regulatory documents essential for dossier preparation. Professionals will be tasked with drafting and submitting regulatory filings to various domestic and international regulatory authorities, as well as preparing amendments, updates, variations, and revisions to existing submissions. A core aspect of the role involves coordinating with cross-functional teams to efficiently resolve regulatory deficiencies and drafting comprehensive responses to regulatory authority queries and customer comments. Additional duties include maintaining and updating regulatory databases, preparing Applicant and Restricted Parts for Abbreviated New Drug Applications (ANDAs), and compiling dossiers in eCTD and CTD formats for global regulatory submissions. Guiding internal teams on current regulatory requirements, planning and monitoring regulatory projects, and evaluating product changes to determine appropriate submission categories are also vital. Reviewing specifications, protocols, stability data, and other regulatory documentation, supporting manufacturing sites during inspections, and ensuring timely regulatory compliance across R&D, Production, QA/QC, and Marketing teams are key functions.
Required Skills:
Candidates should possess strong knowledge of global Regulatory Affairs guidelines and submission requirements, coupled with practical experience in ANDA submissions. Expertise in eCTD and CTD dossier compilation is essential. A robust understanding of regulatory deficiency management, excellent documentation, and technical writing skills are highly valued. Strong cross-functional coordination and stakeholder management abilities, along with a comprehensive understanding of domestic and international regulatory compliance, are also required. Superior communication and analytical skills will be critical for success in this role.
Walk-in Interview Details:
- Date: 18th July 2026 (Saturday)
- Department: Regulatory Affairs – FML Division
- Venue: MSN Laboratories, R&D Center, Pashamylaram, Hyderabad
- Work Location: Pashamylaram, Hyderabad
Documents to Carry:
Applicants are requested to bring their updated Resume/CV, passport-size photographs, government-issued photo ID proof, all educational certificates and mark sheets, experience certificates, latest salary slips, and current CTC details (if applicable).
Contact Person: Dinesh Baratam, Mobile: 9154811048
Why Join Us?
This opportunity offers invaluable exposure to global regulatory submissions, a dynamic and collaborative work environment, and significant career advancement prospects within pharmaceutical regulatory affairs. Join our team and contribute to worldwide product registrations and compliance activities.
