Associate Scientist - Pharmaceutical Development

### Overview
The Associate Scientist contributes to research and development projects by designing and executing experiments, analyzing data, and supporting the development of drug products

CORE RESPONSIBILITIES
- Design and conduct experiments under guidance to develop formulations and analytical methods for drug candidates.
- Prepare tablet and capsule dosage form prototypes using granulators, dryers, and tablet presses.
- Prepare samples, perform assays, and operate laboratory equipment such as dissolution apparatus, DSC, and TGA.
- Analyze data, interpret results, and document findings in laboratory notebooks and technical reports.
- Assist in drafting protocols, standard operating procedures (SOPs), and study reports.
- Contribute to laboratory maintenance, equipment calibration, and inventory management.
- Present data in project meetings and collaborate with cross-functional teams to advance programs.
- Ensure compliance with safety, GLP, and GMP regulations in all laboratory activities.
- Participate in troubleshooting and optimization of experimental procedures to improve data quality and efficiency.
- Draft Master Batch Records and development methods.
- Interface with clients prior to and during development batches.
- Other duties as assigned.

TECHNICAL COMPETENCIES

- Knowledge of pharmaceutical sciences, analytical techniques, and formulation principles, especially those related to solid oral dosage forms containing small molecule drugs.
- Ability to operate common laboratory instruments and perform calculations accurately.
- Ability to interpret data, such as dissolution rate, disintegration time, hardness, etc., related to solid dosage for quality and performance.
- Knowledge of material science attributes, such as polymorphism, particle size, etc., affecting solid oral dosage form quality and performance.
- Familiarity with data analysis software and basic statistical methods.
- Understanding of regulatory and quality requirements for preclinical and clinical development.
- Technical writing skills for documentation, including protocols and reports.

SKILLS AND ABILITIES

- Strong analytical and problem-solving abilities to interpret data and troubleshoot.
- Effective communication and interpersonal skills within cross-functional teams.
- Works collaboratively in team-oriented settings while managing individual tasks.
- Manages time efficiently and adapts to evolving project demands.
- Demonstrates curiosity, adaptability, and commitment to scientific excellence.

EDUCATION AND EXPERIENCE

- Requires Bachelor’s degree in Chemistry, Pharmaceutics, or related field.
- 0–2 years of laboratory experience in pharmaceutical or related industry.
Internship or academic research experience is beneficial