Sr. Manager- FD-ROW- Ophthalmic

Roles & Responsibilities:
• Lead formulation development activities for ophthalmic products for ROW markets
• Plan, execute, and review product development in line with ROW regulatory requirements
• Oversee scale-up, technology transfer, and commercialization activities
• Coordinate with Analytical R&D, QA, Regulatory Affairs, Production, and Packaging teams
• Ensure timely delivery of development milestones and regulatory submissions
• Handle troubleshooting during development, scale-up, and validation stages
• Review and approve development reports, protocols, and technical documentation
• Support regulatory queries, variations, and lifecycle management activities
• Ensure compliance with cGMP, ICH guidelines, and internal quality standards
• Mentor and guide team members to achieve functional and project goals

Qualification:
• M.Pharm (Master's of Pharmacy)

Experience:
• 14+ years of experience in ophthalmic formulation development

Key Skills:
• Strong expertise in ophthalmic dosage forms and sterile formulations
• In-depth knowledge of ROW regulatory guidelines
• Leadership and cross-functional coordination skills
• Strong problem-solving and project management abilities

About the Company:
Ajanta Pharma Ltd is a globally recognized pharmaceutical company with strong R&D capabilities, focused on developing high-quality, differentiated formulations, including ophthalmic products, for regulated and emerging markets.