Pharmaceutical Company Invites Regulatory Affairs Professionals for Walk-in Drive
A leading, research-driven pharmaceutical company, globally recognized for its high-quality Active Pharmaceutical Ingredients (APIs), finished dosage formulations, and specialty medicines, is conducting a walk-in drive. This presents a prime opportunity for experienced professionals to join its Regulatory Affairs department, specifically within the Finished Manufacturing Line (FML) division. The company, known for advanced R&D facilities and a significant international presence, is committed to fostering innovation and ensuring accessible healthcare solutions worldwide.
Positions and Eligibility:
The drive seeks qualified candidates for Executive, Senior Executive, and Junior Manager roles. Applicants must possess 2 to 7 years of hands-on experience in FML Regulatory Affairs and hold a B.Pharm or M.Pharm qualification. All positions are located at the company’s R&D Center in Pashamylaram, Hyderabad.
Core Responsibilities:
Professionals joining this division will be responsible for a comprehensive suite of regulatory activities. This includes collecting necessary documents, preparing and submitting detailed dossiers to both domestic and international authorities, and diligently managing all amendments, updates, variations, and revisions to existing submissions. Key tasks involve coordinating with cross-functional teams to effectively resolve regulatory deficiencies, drafting precise responses to regulatory queries and customer comments, and maintaining accurate regulatory databases. Compiling dossiers in eCTD and CTD formats for global submissions, preparing Applicant and Restricted Parts for Abbreviated New Drug Applications (ANDAs), and guiding internal teams on current regulatory requirements are central to these positions. Candidates will also evaluate product changes for appropriate submission categories, review crucial documentation such as specifications and stability data, and provide support to manufacturing sites during regulatory inspections and audits. Ensuring timely compliance through effective coordination across R&D, Production, QA/QC, and Marketing teams is also a vital aspect of the role.
Essential Skills:
Successful candidates will require strong foundational knowledge of global Regulatory Affairs guidelines, coupled with practical experience in ANDA submissions and proficiency in eCTD and CTD dossier compilation. Essential skills include a solid understanding of regulatory deficiency management, strong documentation and technical writing capabilities, and excellent communication and analytical abilities. The role also demands effective cross-functional coordination, adept stakeholder management, and a comprehensive grasp of both domestic and international regulatory compliance standards.
Walk-in Interview Details:
Interested and eligible candidates are invited to attend a walk-in interview on Saturday, July 18th, 2026.
Venue: The company’s R&D Center, Pashamylaram, Hyderabad.
Documents Required:
Attendees must carry an updated resume/CV, passport-size photographs, a government-issued photo ID proof, all educational certificates and mark sheets, experience certificates, latest salary slips, and current CTC details (if applicable).
Career Growth:
Joining this organization offers a significant opportunity to work with a leading pharmaceutical entity, gain extensive exposure to complex global regulatory filings, and contribute directly to vital product registrations and compliance activities across international markets. It promises a collaborative work environment and a clear path for professional advancement in Regulatory Affairs.
