MSN Laboratories is conducting a Walk-in Drive for experienced professionals in the Regulatory Affairs (FML Division) at its R&D Center, Pashamylaram, Hyderabad. The company is hiring Executive, Senior Executive, and Junior Manager positions for candidates with 2–7 years of experience in Finished Manufacturing Line (FML) Regulatory Affairs. This is an excellent opportunity for B.Pharm and M.Pharm professionals seeking to advance their careers in pharmaceutical regulatory affairs.
About MSN Laboratories
MSN Laboratories is one of India’s leading research-driven pharmaceutical companies, known for developing and manufacturing high-quality Active Pharmaceutical Ingredients (APIs), finished dosage formulations, and specialty medicines. With state-of-the-art R&D facilities, global regulatory approvals, and a presence in multiple international markets, MSN is committed to innovation, quality, and affordable healthcare solutions.
Job Overview
| Particulars | Details |
|---|---|
| Company | MSN Laboratories |
| Division | FML (Finished Manufacturing Line) |
| Department | Regulatory Affairs |
| Job Role | Executive / Senior Executive / Junior Manager |
| Experience | 2–7 Years |
| Qualification | B.Pharm / M.Pharm |
| Job Location | Hyderabad |
| Work Location | MSN R&D Center, Pashamylaram, Hyderabad |
| Interview Mode | Walk-in Interview |
Eligibility Criteria
| Qualification | Experience |
|---|---|
| B.Pharm / M.Pharm | 2–7 Years in FML Regulatory Affairs |
Key Responsibilities
- Collect regulatory documents from various departments for dossier preparation.
- Prepare and submit regulatory filings to domestic and international regulatory authorities.
- Prepare amendments, updates, variations, and revisions to existing submissions.
- Coordinate with Cross-Functional Teams (CFTs) to resolve regulatory deficiencies.
- Draft responses to regulatory authority queries and customer comments.
- Maintain and update regulatory databases.
- Prepare Applicant and Restricted Parts for Abbreviated New Drug Applications (ANDAs).
- Compile dossiers in eCTD and CTD formats for global regulatory submissions.
- Guide cross-functional teams on current regulatory requirements.
- Plan, assign, and monitor regulatory projects within the team.
- Evaluate product changes and determine the appropriate regulatory submission category.
- Review specifications, protocols, stability data, bio-waivers, and other regulatory documentation.
- Support manufacturing sites during regulatory inspections and audits.
- Coordinate with R&D, Production, QA/QC, and Marketing teams to ensure timely regulatory compliance.
- Review and approve change controls and update regulatory files accordingly.
Required Skills
- Strong knowledge of global Regulatory Affairs guidelines and submission requirements.
- Hands-on experience in ANDA submissions.
- Expertise in eCTD and CTD dossier compilation.
- Good understanding of regulatory deficiency management.
- Strong documentation and technical writing skills.
- Cross-functional coordination and stakeholder management.
- Knowledge of domestic and international regulatory compliance.
- Excellent communication and analytical skills.
Key Performance Indicators (KPIs)
- Ensure regulatory submissions are completed within defined timelines.
- Demonstrate strong understanding of market-specific regulatory requirements.
- Provide effective action plans for addressing regulatory deficiencies.
- Maintain high-quality regulatory documentation and compliance standards.
Walk-in Interview Details
| Particulars | Information |
|---|---|
| Interview Date | 18th July 2026 (Saturday) |
| Department | Regulatory Affairs – FML Division |
| Interview Venue | MSN Laboratories, R&D Center, Pashamylaram, Hyderabad |
| Work Location | Pashamylaram, Hyderabad |
Contact Details
| Contact Person | Mobile Number |
|---|---|
| Dinesh Baratam | 9154811048 |
Documents to Carry
Candidates are requested to bring:
- Updated Resume/CV
- Passport-size Photographs
- Government-issued Photo ID Proof
- Educational Certificates and Marksheets
- Experience Certificates
- Latest Salary Slips
- Current CTC Details (if applicable)
Why Join MSN Laboratories?
- Opportunity to work with a leading research-driven pharmaceutical company.
- Exposure to global regulatory submissions, including ANDA, eCTD, and CTD filings.
- Collaborative work environment with cross-functional teams.
- Career growth in Regulatory Affairs for domestic and international markets.
- Opportunity to contribute to global pharmaceutical product registrations and compliance activities.