MSN Walk-in AR&D & Regulatory Affairs / 5 days ago
MSN Labs AR&D & Regulatory Affairs Jobs | M.Pharm | Hyderabad
MSN Laboratories is hiring M.Pharm candidates with 2–7 years of experience for Analytical R&D and Regulatory Affairs (Formulation) roles in Hyderabad.
MSN Laboratories Pvt. Ltd. is conducting a Walk-in Drive for experienced M.Pharm professionals in the Analytical Research & Development (Formulation) and Regulatory Affairs (Formulation) departments. The recruitment drive will be held in Kukatpally, Hyderabad, offering an excellent opportunity for candidates with 2–7 years of pharmaceutical formulation experience to join one of India’s leading research-driven pharmaceutical companies.
Professionals with expertise in analytical method development, formulation development, regulatory dossier preparation, CTD/eCTD submissions, pharmaceutical R&D, quality documentation, and regulatory compliance are encouraged to attend the interview. If you are looking to advance your career in pharmaceutical research, formulation development, analytical sciences, or drug regulatory affairs, this walk-in drive offers an excellent platform.
Company Overview
MSN Laboratories Pvt. Ltd. is one of India’s fastest-growing research-based pharmaceutical companies with a strong presence in Active Pharmaceutical Ingredients (APIs), Finished Dosage Formulations (FDF), Contract Research, and Pharmaceutical Research & Development. The company operates state-of-the-art manufacturing facilities and R&D centers that comply with international regulatory standards including USFDA, EMA, WHO-GMP, MHRA, and other global regulatory authorities.
Recognized as a Great Place to Work® Certified 2025 organization, MSN Laboratories invests heavily in innovation, scientific research, and talent development. Employees gain exposure to advanced pharmaceutical technologies, formulation research, regulatory submissions, analytical method development, and global product registration activities.
Job Role & Responsibilities
Analytical Research & Development (Formulation)
Qualification
Experience
Key Responsibilities
- Develop and validate analytical methods for pharmaceutical formulations.
- Perform analytical testing of formulation development batches.
- Conduct method transfer, method verification, and stability studies.
- Prepare analytical protocols and technical reports.
- Operate analytical instruments including HPLC, UPLC, Dissolution Apparatus, UV Spectrophotometer, and related laboratory equipment.
- Support formulation development teams with analytical evaluation.
- Review analytical data and ensure compliance with Good Laboratory Practices (GLP).
- Maintain laboratory documentation in accordance with regulatory requirements.
- Participate in technology transfer and product development projects.
Regulatory Affairs – Formulation
Qualification
Experience
Key Responsibilities
- Prepare and compile regulatory dossiers for domestic and international markets.
- Develop and review CTD, eCTD, ACTD, and product registration documentation.
- Coordinate with cross-functional teams including R&D, QA, QC, Manufacturing, and Packaging.
- Review pharmaceutical product labeling and regulatory documents.
- Respond to regulatory authority queries and deficiency letters.
- Maintain compliance with changing global pharmaceutical regulations.
- Support product lifecycle management and regulatory strategy.
- Ensure timely submission of product registrations and variations.
Eligibility / Qualifications
Candidates meeting the following criteria are eligible to attend the walk-in interview.
Educational Qualification
Relevant Courses
M.Pharm, Pharmaceutics, Pharmaceutical Analysis, Pharmaceutical Chemistry, Drug Regulatory Affairs, Industrial Pharmacy, Pharmaceutical Quality Assurance, Pharmaceutical Technology, Pharmaceutical Sciences, Analytical Chemistry, Formulation Development, Regulatory Affairs.
Experience
- 2–7 Years in:
- Analytical Research & Development (Formulation)
- Regulatory Affairs (Formulation)
Preferred Skills
Candidates with experience in the following areas will be preferred:
- Analytical Research & Development
- Formulation Development
- Pharmaceutical R&D
- Analytical Method Development
- Method Validation
- Stability Studies
- HPLC
- UPLC
- Dissolution Testing
- UV Spectroscopy
- CTD
- eCTD
- ACTD
- Regulatory Affairs
- Global Regulatory Submissions
- Product Registration
- Pharmaceutical Documentation
- Drug Regulatory Compliance
- Good Laboratory Practices (GLP)
- Good Manufacturing Practices (GMP)
Why Join MSN Laboratories?
MSN Laboratories provides professionals with an opportunity to work in a highly research-oriented pharmaceutical organization focused on innovation and global regulatory excellence.
Employees benefit from exposure to:
- Pharmaceutical Research & Development
- Formulation Development
- Analytical Method Development
- Drug Product Development
- Pharmaceutical Regulatory Affairs
- CTD & eCTD Submissions
- Global Product Registrations
- Stability Studies
- HPLC & UPLC Analysis
- Pharmaceutical Documentation
- GMP & GLP Compliance
- Technology Transfer
- International Regulatory Standards
Being part of a Great Place to Work® Certified organization also offers strong career progression, learning opportunities, and exposure to global pharmaceutical projects.
Location & Salary
Location: Hyderabad, Telangana
Estimated Salary: Approximately ₹5–10 LPA, depending on experience, technical expertise, and interview performance.
Application Process
Eligible candidates can attend the walk-in interview with the required documents.
Walk-in Details
Date: 18 July 2026 (Saturday)
Time: 9:30 AM – 4:00 PM
Interview Venue
Qualychrome Research Labs
H.No. 5-5-35/128, Plot No. 177,
Near Venkateswara Swamy Temple,
Prashanti Nagar, Kukatpally,
Hyderabad, Telangana – 500072.
Job Location
MSN Laboratories Pvt. Ltd.
R&D Center, Hyderabad, Telangana.
Documents Required
Candidates should carry:
- Updated Resume
- Educational Certificates (Photocopies)
- Passport Size Photographs
- Aadhaar Card Copy
- PAN Card Copy
Contact Details
Uma Devi – [email protected]
Dinesh Baratam – [email protected]
Frequently Asked Questions (FAQs)
1. Which departments are hiring at MSN Laboratories?
MSN Laboratories is hiring for Analytical Research & Development (Formulation) and Regulatory Affairs (Formulation).
2. What qualification is required?
Candidates must possess an M.Pharm degree.
3. What experience is required?
Applicants should have 2–7 years of relevant experience in Formulation AR&D or Regulatory Affairs.
4. Is experience in CTD/eCTD preparation preferred?
Yes. Candidates applying for Regulatory Affairs should have experience in CTD, eCTD, and global regulatory submissions.
5. What documents should candidates carry for the interview?
Candidates should bring an updated resume, educational certificates, passport-size photographs, Aadhaar card copy, and PAN card copy.
6. Where will the interview be conducted?
The walk-in interview will be held at Qualychrome Research Labs, Kukatpally, Hyderabad.
Summary
| Company | MSN Laboratories Pvt. Ltd. |
| Department Vacancies | Analytical Research & Development (Formulation), Regulatory Affairs (Formulation) |
| Qualification | M.Pharm |
| Experience | 2–7 Years |
| Location | Hyderabad, Telangana |
