Sr. Supervisor, Manufacturing (Night shift)

Role: Senior Supervisor overseeing GMP manufacturing operations during the Red Night shift for clinical and commercial parenteral products. Responsibilities: supervise manufacturing associates, schedule and direct daily activities, ensure GMP compliance and safety, review batch documentation, coordinate with cross-functional departments (quality, validation, engineering), and oversee validation and troubleshooting efforts. Requirements: Bachelor's degree in STEM plus 4 years of GMP manufacturing experience, or associates with 6 years, or high school diploma with 8 years. Skills: strong leadership, organization, accountability, and GMP knowledge; technical experience in drug product/parenteral filling preferred. High-Value: manufacturing of injectable biological or small molecule therapeutics, GMP compliance, validation oversight, cGMP documentation, safety protocols, and experience with electronic systems (e.g., Oracle, Trackwise). Shift work on a 12-hour rotation with some coordination with other departments necessary. This role is critical to product quality and compliance in a regulated biopharma environment.