Manufacturing Associate I-OSD 3rd Shift

Role: Manufacturing Associate in a GMP environment supporting pharmaceutical production, with responsibilities including bulk drug formulation, packaging, equipment cleaning, and facility maintenance. The position involves adhering to cGMPs and GDPs, documenting work, and assisting with validations and environmental monitoring. Requirements: High School diploma or equivalent; 0-5 years of experience in pharmaceutical manufacturing, with higher levels favoring relevant science/technical degrees and experience in OSD production. Skills include basic knowledge of GMPs, chemistry, biology, safety regulations, mechanical aptitude, and proficiency with computer systems (e.g., Microsoft, SAP). Preferred qualifications include familiarity with Master Batch Records, good documentation, teamwork, and adaptability. High-value specifics: Entry to senior-level roles with exposure to oral solid dose (OSD) manufacturing, working in a GMP setting, possibly involving potent compounds requiring specialized gowning and safety procedures. Work setup: shift-based, with physical requirements such as lifting, equipment operation, and gowning, in a manufacturing environment.