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Scientist

K3-Innovations · Irvine, CA

CONTRACT Posted Sep 9, 2026

Job Description

Scientist – Sterile Liquid Formulation & Process Development

Schedule: Monday–Friday, 8:00 AM–5:00 PM

Experience: 2–5+ years of relevant industry experience





Position Summary

We are seeking a Scientist with hands-on experience in
pharmaceutical formulation and manufacturing process development, with a focus on
sterile liquid drug products such as solutions, emulsions, and suspensions.

The ideal candidate will have experience with sterile processing and sterilization techniques, analytical characterization of liquid formulations, and hands-on laboratory experience with
HPLC/UPLC. This role requires strong experimental skills, scientific problem-solving, accurate documentation, and the ability to independently plan and execute laboratory studies.





Key Responsibilities


- Plan and execute laboratory experiments supporting sterile liquid formulation and manufacturing process development.
- Develop and characterize sterile liquid dosage forms, including solutions, emulsions, and suspensions.
- Perform analytical and characterization studies to generate accurate, scientifically sound data.
- Evaluate formulation and process parameters and interpret experimental results.
- Apply scientific problem-solving and statistical approaches to support formulation and process development.
- Perform characterization using techniques such as pH, osmolality, viscosity/rheology, turbidity, particle size, and physical appearance.
- Perform hands-on HPLC/UPLC analysis using detectors such as UV, PDA, and RI.
- Independently plan, execute, analyze, and interpret laboratory experiments as required.
- Maintain accurate and timely documentation in electronic laboratory notebooks (ELNs) while ensuring data integrity.
- Prepare technical reports and communicate experimental results, conclusions, and recommendations.
- Present data and participate in project and team meetings.
- Maintain laboratory equipment and instrumentation to ensure operational readiness.
- Follow all applicable company, safety, quality, and regulatory requirements.






Required Qualifications


- Bachelor's degree in Chemistry, Chemical Engineering, Pharmacy, or a related scientific discipline with
3–5 years of relevant industry experience, OR
- Master's degree in Chemistry, Chemical Engineering, Pharmacy, or a related scientific discipline with
2+ years of relevant industry experience.
- Hands-on experience in pharmaceutical formulation and/or process development.
- Experience with sterile liquid drug products preferred.
- Strong laboratory experimentation and data analysis skills.
- Strong technical writing and verbal/written communication skills.
- Proficiency with Microsoft Word and Excel.
- Ability to work independently while effectively collaborating with cross-functional teams.






Preferred Qualifications


- Experience with sterile liquid solutions, emulsions, or suspensions.
- Experience with filtration and/or autoclave sterilization.
- Hands-on HPLC/UPLC experience, including UV, PDA, or RI detectors.
- Experience with formulation characterization including:
- pH
- Osmolality
- Viscosity/Rheology
- Turbidity
- Particle Size
- Physical Appearance
- Experience with statistical analysis and statistical software.
- Experience analyzing experimental data and preparing technical reports.
- Experience working in a GMP/pharmaceutical development environment.






Core Skills

Sterile Liquid Formulation Pharmaceutical Formulation Process Development Sterile Manufacturing Filtration Autoclaving HPLC UPLC pH Osmolality Viscosity/Rheology Turbidity Particle Size Data Analysis Technical Documentation GMP Statistical Analysis

Additional Details

City
Irvine
State
California
Country
US
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