Parenteral Manufacturing Technician

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Rotating schedule- horario rotativo MAJOR DUTIES AND RESPONSIBILITIES      State the most important activities and accountabilities of this position.  Describe how these activities and accountabilities can influence the achievement of departmental or business goals.  (Attach additional sheets if needed): 1. Execute Parenteral Manufacturing Operations Performs routine and critical operational activities required for the setup, operation, and cleaning of parenteral manufacturing equipment to ensure consistent, efficient, and compliant production processes. •            Conducts equipment setup, changeover, cleaning, and line clearance following approved SOPs and safety procedures. •            Operates formulation, preparation, and filling equipment; performs basic troubleshooting and escalates abnormalities. •            Cleans, sanitizes, and sterilizes classified manufacturing areas and equipment in compliance with aseptic and contamination control standards. •            Operates autoclaves and executes sterilization cycles for manufacturing components and equipment. •            Performs Cleaning-in-Place (CIP) and Sterilization-in-Place (SIP) operations for tanks and systems. •            Executes pre  and post use filter integrity testing. •            Receives, verifies, handles, and weighs excipients and drug substances/active ingredients for formulation steps. •            Executes formulation processes per batch record instructions, including pH adjustment, yield calculations, mixing parameters, in process controls, and volume adjustments. •            Collects required in process samples following aseptic sampling techniques.             Percentage of time •            Interacts with automated and computer controlled equipment, ensuring adherence to data integrity principles. 2. Documentation, Compliance, and Process Control Ensures complete, accurate, and compliant execution of batch records and associated documentation, supporting data integrity and audit readiness across all operations. •            Maintains accurate inventory of components and materials; submits timely requests to support uninterrupted operations. •            Completes all production records and system transactions accurately, legibly, and in real time following Good Documentation Practices (GDP). •            Verifies accuracy and completeness of manufacturing documentation, including computer generated transactions. •            Performs batch record audits, as required. •            Ensures assigned equipment is cleaned, labeled, calibrated, and qualified before use. •            Identifies opportunities to improve procedures and contributes to the development or revision of SOPs. 3. Support Manufacturing and Cross Functional Activities Provides support to quality, validation, operational, and training activities that ensure efficient and compliant manufacturing. •            Initiates and participates in quality investigations, providing technical input and timely documentation. •            Supports onboarding and “on the job” training of new employees. •            Participates in internal, external, and regulatory