Pharmaceutical Development Senior Associate Scientist II

Catalent

Catalent seeks a Pharmaceutical Development Senior Associate Scientist II to support oral solid drug product formulation and development at its Kansas City facility. The role involves laboratory execution, technical documentation, training, and GMP compliance with a 12pm-10:30pm shift schedule.

Responsibilities

Execute laboratory work plans and schedules with supervisory input
Draft technical documents including batch records, reports, and standard operating procedures
Train others on laboratory procedures and techniques
Perform physical testing including density analysis, flow analysis, and sieve analysis
Conduct manufacturing documentation review and quality verification for regulatory compliance

Requirements

Bachelor's degree in life or physical science with 4+ years related experience, or Master's degree with 2+ years experience
Strong knowledge of pharmaceutics principles and concepts
Ability to apply mathematical and scientific reasoning to pharmaceutical problems
Advanced understanding of equipment operation and instrument troubleshooting across multiple techniques
Excellent written and verbal communication with internal and external stakeholders
Understanding of current Good Manufacturing Practices and GMP workspace operations

Apply

Vacancy posted 5 days ago

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