The Full-Time Pharmacist supports Medivant’s sterile injectable manufacturing operations by ensuring all compounding, labeling, and documentation processes comply with FDA regulations, USP <797>/<800>, and internal SOPs. This role involves verifying batch records, supervising compounding operations, ensuring quality assurance compliance, and overseeing controlled substance handling as required. This is a full-time position offering long-term career growth, stability, and the opportunity to work in a highly regulated cGMP manufacturing environment.
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
1-10 employees