Macleods Hiring Pharma Graduates | Walk-in Drive for Regulatory Affairs Roles
Looking for a Regulatory Affairs Job? This Walk-In Drive by Macleods Pharmaceuticals offers an excellent opportunity for experienced pharmacy professionals to join its R&D team in Mumbai. Candidates with M.Pharm and M.Sc. qualifications and relevant Regulatory Affairs or Pharmaceutical Development experience are invited to attend the Walk-In Drive on 04th July 2026. Check the complete eligibility criteria, interview details, registration process, and venue below.
- Position: Officer/Executive
- Department: Regulatory Affairs (USA Market)
- Location: R&D-Plot 60 Mumbai
About the Company
Macleods Pharmaceuticals is one of India’s leading pharmaceutical companies with a strong global presence across regulated and emerging markets. The company is well known for its research-driven approach, high-quality manufacturing facilities, and continuous innovation in pharmaceutical development. Macleods offers excellent career opportunities for professionals looking to build their careers in Research & Development and Regulatory Affairs.
Job Description
Macleods Pharmaceuticals is conducting a Walk-In Drive for experienced professionals to join its R&D Centre in Mumbai. The company is hiring for Regulatory Affairs (USA Market) positions. Candidates with M.Pharm or M.Sc. qualifications and relevant experience in pharmaceutical regulatory affairs, ANDA submissions, formulation & development, and regulated markets are invited to attend the walk-in interview.
Key Responsibilities
- Prepare, review, and submit regulatory documents to the US FDA in compliance with current guidelines.
- Compile and manage original ANDA submission modules and supporting documentation.
- Ensure regulatory submissions meet changing FDA requirements and industry standards.
- Coordinate with cross-functional teams to gather technical and scientific data for submissions.
- Review product dossiers for solid oral dosage forms, injectables, and MDI (Metered Dose Inhalers).
- Maintain regulatory records and ensure timely responses to health authority queries.
- Monitor updates in US regulatory guidelines and implement necessary compliance changes.
- Support lifecycle management activities, including post-approval submissions and regulatory variations.
- Ensure all regulatory documentation is accurate, complete, and submitted within project timelines.
- Collaborate with R&D, Quality Assurance, and Manufacturing teams to support successful product registrations.
Qualification
- M. Pharm/M.Sc.
Experience
- 2-8 Years of experience in Pharmaceutical Regulatory Affairs
Interview Details
- Interview Date: 04th July 2026 (Saturday)
- Interview Time: 09:30 AM onwards
- Interview Venue: Plot 60, Street No 14, MIDC Phase II, Andheri East, Mumbai-400093
Documents to Carry
Candidates are requested to carry:
- Updated CV
- Salary Structure (CTC Break-up)
- Aadhaar Card
Contact Information
- Contact number: 8291331272/7208877803/8291054728
Registration Link
Interested candidates need to register through the QR code or link (works best on Google Chrome) given: LINK
