Manufacturing Associate-2nd Shift-Bulk

Role: Manufacturing Associate supporting sterile pharmaceutical production in a cGMP environment, primarily on 2nd shift (2:00pm-12:30am). Objectives include performing equipment cleaning, setup, automation operation, batch processing, sample collection, process monitoring, minor equipment maintenance, and documentation compliance. Responsibilities encompass following SOPs, maintaining detailed records, executing tasks with precision, ensuring safety, and supporting development and validation activities. Requirements: High school diploma or equivalent; 0-5 years in pharmaceutical manufacturing, with preferred experience in sterile operations. Skills needed include mechanical aptitude, knowledge of cGMP and safety regulations, computer proficiency, and aseptic gowning. Qualifications vary by experience level, with higher preferred experience and technical discipline degrees. High-value specifics: sterile biopharma manufacturing, cGMP compliance, shift-based work, physical demands including lifting and standing, and potential for weekend shifts. The role involves independent work with team collaboration, adhering to safety and SOP standards.