Associate Scientist - Pharmaceutical Development

AustinPx Pharmaceutics and Manufacturing•Georgetown, TX

About The Position

The Associate Scientist contributes to pharmaceutical research and development projects by designing and executing experiments, analyzing data, and supporting the development of drug products. The role focuses on formulations and analytical methods for drug candidates, particularly solid oral dosage forms containing small-molecule drugs. The Associate Scientist prepares dosage-form prototypes, performs laboratory assays, documents results, and supports development programs in collaboration with cross-functional teams and clients. Laboratory work must comply with safety, GLP, and GMP requirements.

Requirements

  • Bachelor’s degree in Chemistry, Pharmaceutics, or a related field.
  • 0–2 years of laboratory experience in the pharmaceutical or a related industry.
  • Knowledge of pharmaceutical sciences, analytical techniques, and formulation principles, especially for solid oral dosage forms containing small-molecule drugs.
  • Ability to operate common laboratory instruments and perform calculations accurately.
  • Ability to interpret solid-dosage data, including dissolution rate, disintegration time, and hardness, in relation to quality and performance.
  • Knowledge of material-science attributes, such as polymorphism and particle size, that affect 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.
  • Strong analytical and problem-solving abilities to interpret data and troubleshoot.
  • Effective communication and interpersonal skills within cross-functional teams.
  • Ability to collaborate in team-oriented settings while managing individual tasks.
  • Ability to manage time efficiently and adapt to evolving project demands.
  • Curiosity, adaptability, and commitment to scientific excellence.

Nice To Haves

  • Internship or academic research experience.

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.
  • Perform other duties as assigned.
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