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

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