Pharmaceutical Development Senior Associate Scientist Ii
Catalent, Inc.
San Diego, California, US
Pharmaceutical principles
Laboratory documentation
Cgmp compliance
The Senior Associate Scientist II supports formulation design and development of oral solid drug products and trains others in clinical trial manufacturing operations using sound pharmaceutical principles
Job Summary
The Senior Associate Scientist II supports formulation design and development of oral solid drug products and trains others in clinical trial manufacturing operations using sound pharmaceutical principles.
Ensure all work is carried out in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs), maintaining high quality laboratory documentation.
Catalent offers competitive medical benefits and 401K, 152 hours PTO + 8 Paid Holidays, and a dynamic, fast-paced work environment with opportunities to work on Continuous Improvement Processes.
Matching Summary
The Senior Associate Scientist II supports formulation design and development of oral solid drug products and trains others in clinical trial manufacturing operations using sound pharmaceutical principles.
Skills & Requirements
Must-have
Pharmaceutical principles
Laboratory documentation
cGMP compliance
SOP adherence
Technical document drafting
Execute procedures and methods
Nice-to-have
Continuous Improvement Processes
Personal initiative
Dynamic pace
Meaningful work
Key Requirements
Bachelor's degree with 4+ years related work experience
Master's degree with 2+ years related work experience