Macleods Pharmaceuticals has announced a Walk-In Drive for experienced Regulatory Affairs and Pharmaceutical Development Research (PDR) professionals at its R&D Centre in Mumbai. Candidates with M.Pharm or M.Sc qualifications and relevant experience in US FDA Regulatory Affairs, ANDA submissions, formulation development, and regulated markets are invited to attend the interview on 4th July 2026.
This is an excellent opportunity for pharmaceutical professionals looking to build a rewarding career with one of India’s leading pharmaceutical companies working on regulated global markets.
Macleods R&D Walk-In Drive 2026 – Overview
| Particular | Details |
|---|---|
| Company | Macleods Pharmaceuticals |
| Department | Regulatory Affairs (USA Market), PDR |
| Job Location | R&D Centre, Plot 60, MIDC Phase II, Andheri East, Mumbai |
| Qualification | M.Pharm / M.Sc |
| Experience | 2–8 Years |
| Interview Date | 04 July 2026 (Saturday) |
| Reporting Time | 09:30 AM Onwards |
| Job Type | Full-Time |
| Selection Mode | Walk-In Interview |
Available Positions
1. Officer / Executive – Regulatory Affairs (USA Market)
Qualification
- M.Pharm
- M.Sc
Experience
- 2–8 Years
Key Responsibilities
- Prepare and submit regulatory documentation to global regulatory authorities.
- Compile and review ANDA submission modules.
- Prepare original ANDA dossiers.
- Ensure compliance with changing US FDA regulatory requirements.
- Support submissions for Solid Oral Dosage, Injectable and MDI products.
- Coordinate with cross-functional departments for timely submissions.
- Maintain regulatory documentation and compliance records.
2. Research Associate / Senior Research Associate – PDR
Qualification
- M.Pharm
Experience
- 4–7 Years
Key Responsibilities
- Formulation development of Solid Oral Dosage forms.
- Development of Liquid Oral formulations.
- Execute product development activities for regulated markets.
- Conduct formulation optimization and technology transfer support.
- Prepare development reports and technical documentation.
- Coordinate analytical and manufacturing activities during product development.
Required Qualifications
Candidates should possess:
- M.Pharm
- M.Sc (Applicable for Regulatory Affairs)
Applicants should have experience in:
- Pharmaceutical Regulatory Affairs
- ANDA Compilation
- US FDA Guidelines
- Formulation Development
- Solid Oral Dosage Forms
- Liquid Oral Formulations
- Injectable Products
- Regulated Market Documentation
Why Join Macleods Pharmaceuticals?
- Opportunity to work on US regulated market products.
- Exposure to ANDA submissions and FDA regulatory projects.
- Work with experienced R&D scientists.
- Career growth in Pharmaceutical Research & Development.
- Modern R&D infrastructure.
- Learning opportunities in formulation and regulatory sciences.
- Competitive salary and employee benefits.
Walk-In Interview Details
Interview Date
04 July 2026 (Saturday)
Time
09:30 AM Onwards
Venue
Macleods Pharmaceuticals R&D Centre
Plot No. 60, Street No. 14
MIDC Phase II
Andheri East
Mumbai – 400093
