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Associate Scientist - Pharmaceutical Development

Job in Georgetown, Williamson County, Texas, 78628, USA
Listing for: AustinPx Pharmaceutics and Manufacturing
Full Time position
Listed on 2026-11-01
Job specializations:
  • Research/Development
    Pharmaceutical Science/ Research, Research Scientist, Clinical Research
Salary/Wage Range or Industry Benchmark: 65000 - 85000 USD Yearly USD 65000.00 85000.00 YEAR
Job Description & How to Apply Below
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

Position Requirements
10+ Years work experience
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