Associate I, Manufacturing

Role: Manufacturing Associate on night shift in biopharma production, focused on biologics. Objectives: execute sterile manufacturing processes safely, efficiently, and in compliance with cGMP standards. Responsibilities: operate and maintain production equipment, perform cleaning, sterilization, setup, and disassembly; document activities per SOPs and BPRs; handle hazardous biologics and chemicals; interface with automation and business systems (e.g., PAS, BAS, LIMS, SAP); support qualification and validation activities; identify and communicate process issues; contribute to root cause investigations and CAPAs; promote team collaboration aligned with company values. Requirements: high school diploma/GED or associate’s degree with 1+ years’ transferable skills, or bachelor’s degree with no experience; experience in pharmaceutical, biotech, or sterile manufacturing preferred; knowledge of cGMP, SOPs, and documentation processes preferred; basic mechanical or electronic skills advantageous. High-Value: biologics manufacturing, sterile process, cGMP compliance, process automation systems, validation support, shift: night (6PM-6AM, 2-2-3 schedule). Work setup: night shift in manufacturing environment, with responsibilities supporting high-quality biologic production.