Associate Scientist - Pharmaceutical Development
AustinPx
With an account: save jobs, track applications, build tailored resumesAlready have an account? Log in
- Location
- Georgetown, TX
- Posted
- Oct 30
- Today
Build resumeBuild cover letterGenerate interview prepBuild resumeBuild cover letterGenerate interview prep
Career path
See where this role leads
Jigup maps the next three moves from a job like this one, with the titles and the skills each step asks for.
About the company
AustinPx
Pharmaceuticals · 51 to 200 employees
What you'll do
- 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.
What you need
- 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: a bachelor's degree
Key skills
Pharmaceutical sciencesAnalytical techniquesFormulation principlesSolid oral dosage formsLaboratory instrumentsData analysis softwareBasic statistical methodsTechnical writingAnalytical and problem-solving abilitiesCommunication and interpersonal skills
Keywords for your resumePro
The words this employer's screening is likely to look for.
This job lists resume keywords
The terms this posting uses, pulled out so you can mirror them in your resume. Jigup Pro members see the list on the job board.
See full description on company page, apply now
Read the full posting here
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