Manufacturing Associate II / III, Visual Inspections and Packaging (Days)

Role: Visual Inspection Manufacturing Associate in biopharma drug product manufacturing, primarily responsible for manual and automated visual inspection of sterile parenteral containers to ensure GMP compliance. Core responsibilities include performing inspections, supporting automated equipment, executing packaging activities, documenting GMP data, and maintaining a clean, compliant environment. Qualifications: For Associate II, a Bachelor's, BioWorks Certificate, or high school diploma with relevant experience; for Associate III, similar education with 1+ years of GxP experience, strong documentation skills, and GMP knowledge. Preferred skills include prior parenteral filling experience and familiarity with systems like TrackWise, DeltaV, and LIMS. Experience in sterile, GMP, and cleanroom environments is essential. Work setup involves 10-hour shifts on a 2-2-3 schedule in RTP, with a focus on sterile drug product processes within the drug development and manufacturing stages. The role emphasizes teamwork, compliance, and operational excellence, with a focus on delivering quality therapies to patients.