About this role
Required Competencies
- Strong understanding of formulation and process development of sterile injectable dosage forms for regulated markets.
- Hands-on experience and/or exposure to complex injectable systems, including microspheres, liposomes, and polymer-based formulations.
- Good understanding of pharmaceutical development documentation, technology transfer, and regulatory expectations.
- Working knowledge of Quality by Design (QbD) principles and their application throughout product development.
- Effective cross-functional collaboration, communication, and project coordination skills.
- Ability to work in a highly regulated GMP environment with strong focus on compliance, quality, and attention to detail.
- Experience in formulation optimization, characterization, and troubleshooting of injectable drug products.
- Knowledge of scale-up activities, process validation concepts, and technology transfer requirements is preferred.
Education:
- M. Pharm M. Pharma - Required
- Ph. D. Ph. D. - Preferred
Experience:
- 10 years or more in 10 - 12 Years
Specialized Knowledge: Licenses: