Designing and executing formulation studies to optimize drug product performance, stability, and manufacturability.

Developing robust analytical methods for drug product characterization and quality control.

Conducting pre-formulation studies to assess drug substance properties and compatibility with excipients.

Troubleshooting formulation and process-related issues during development and scale-up.

Preparing technical reports, documentation, and presentations to communicate research findings.

Staying updated with the latest advancements in formulation technologies and regulatory guidelines.

Designing robust and stable formulations, considering factors like solubility, bioavailability, and stability.

Conducting analytical tests to ensure the quality, purity, and stability of drug formulations.

Optimizing manufacturing processes to improve efficiency, reduce costs, and maintain product quality.

Performing stability studies to determine the shelf life and storage conditions of pharmaceutical products.

Ensuring compliance with regulatory requirements, such as those set by FDA or similar agencies.

Transferring formulation and manufacturing knowledge to production teams for scale-up and commercialization.

Identifying and resolving formulation and manufacturing issues during development and production.

Maintaining detailed records of formulation development, testing, and manufacturing processes.

Staying updated with the latest scientific literature and advancements in formulation technology.

Collaborating with cross-functional teams, including research, manufacturing, and marketing, to achieve project goals.

Participating in scale-up activities to transition formulations from lab scale to commercial production.