Scientist, Research Scientist, Pharmaceutical Science​/ Research

The Scientist1 designs and executes experiments, analyzes data, and contributes to the development and optimization of pharmaceutical formulations and processes.

• Plan and perform experiments to develop drug formulations, processing methods, and analytical assays.

• Generate and interpret data; adjust experimental plans based on findings and scientific rationale.

• Contribute to scale‑up and technology transfer activities by supporting engineering studies and data analysis.

• Write technical documents such as protocols, study reports, and CMC sections for regulatory submissions.

• Ensure proper calibration and maintenance of laboratory equipment and instruments.

• Collaborate with cross‑functional teams including analytical, manufacturing, and quality to advance projects.

• Present results at project meetings and provide scientific input to guide project direction.

• Ensure adherence to GLP/GMP and safety requirements in all experimental activities.

• Draft Master Batch Records and development methods.

• Interface with clients prior to and during development batches.

• Other duties as assigned.

• Competence in pharmaceutical sciences, including formulation development and analytical methods, with emphasis on solid oral dosage forms containing small molecule drugs.

• Ability to design experiments, execute the preparation of prototypes, and apply statistical tools for data analysis and interpretation, including evaluation of dissolution, disintegration, hardness, friability, and related performance metrics.

• Familiarity with formulation principles and process development specific to solid oral dosage manufacturing (e.g., blending, granulation, compression, encapsulation, coating).

• Understanding of material science attributes—such as particle size, morphology, hygroscopicity, and polymorphism—and their impact on solid oral dosage form quality and performance.

• Proficient in technical writing and documentation for scientific and regulatory purposes, including protocols, reports, and development summaries.

• Knowledge of regulatory guidelines for early‑phase development and CMC documentation, particularly as they relate to solid oral dosage forms.

• Analytical thinker who works independently and collaboratively as part of a team.

• Communicates scientific information clearly to colleagues and stakeholders.

• Adaptable and responsive to project changes and evolving priorities.

• Demonstrates initiative and curiosity in exploring new ideas and approaches.

• Manages multiple tasks and meets project deadlines effectively.

• Bachelor’s or Master’s degree in Chemistry, Pharmaceutics, or related field.

• 2–5 years of experience in pharmaceutical research or development.

• Experience in formulation and process development is advantageous.