Manufacturing Associate II

Role: Manufacturing Associate II in DP Operations supporting biologics manufacturing within a cGMP environment. Responsibilities: perform routine unit operations such as formulation, sterile filtration, aseptic filling, visual inspection, equipment checks, material staging, and facility cleaning; ensure accurate documentation, support deviation investigations, and participate in SOP updates and continuous improvement; collaborate with QA, QC, and cross-functional teams to maintain compliance and operational efficiency. Requirements: associate or bachelor’s degree in a scientific field or equivalent experience; 2-4 years GMP manufacturing experience preferred, with training available for entry-level candidates; ability to work in cleanrooms, lift up to 35 lbs, and stand for extended periods; proficiency with basic computer systems; vision acuity confirmed via testing. Work setup: 100% onsite role requiring 12-hour night shifts (6:00 PM - 6:00 AM), with flexibility for overtime, weekends, and holidays. High-value biopharma specifics: biologics manufacturing, aseptic processing, cleanroom environment, adherence to cGMP, and cross-functional collaboration. The role emphasizes compliance, operational excellence, and team-based support in a fast-paced manufacturing setting.