Associate Scientist - Pharmaceutical Development

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. Knowledge of pharmaceutical sciences, analytical techniques, and formulation principles, especially those related to solid oral dosage forms containing small molecule drugs.

Overview

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

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