Location: Perungudi, Chennai
Experience Required: 5 to 8 years
Open Positions: 5

Key Responsibilities

• Develop complex injectable and sterile dosage forms (e.g., suspensions, emulsions, peptides).
• Special preference for candidates experienced in onco-injectable products (lyo and non-lyo).
• Implement robust formulation development strategies in alignment with regulatory guidelines (e.g., Quality by Design, FDA).
• Ensure end-to-end project completion as per product development timelines.
• Conduct rigorous experimental studies to meet project objectives.
• Collaborate closely with cross-functional teams, including Technical Services, Operations, and Regulatory Affairs.
• Plan and oversee optimization, scale-up batches, and submission batches, including troubleshooting during all activities.
• Prepare, review, and approve development, scale-up, and submission-related documents.
• Lead technology transfer activities effectively.
• Stay up-to-date with FDA and regulatory guidelines.

What We Are Looking For

• Strong technical background in developing sterile and complex injectable products.
• Hands-on experience with regulatory-driven product development.
• Ability to drive projects to timely completion with cross-functional collaboration.

Interested candidates can share their CVs at:
sarveswaran.rt@caplinpoint.net