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. Schedule-5pm-5am- rotating days- dias rotativos 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. Interacts with automated and computer‑controlled equipment, ensuring adherence to data integrity principles. Documentation, Compliance, and Process Control 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. Interacts with automated and computer‑controlled equipment, ensuring adherence to data integrity principles. 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. 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 inspections. Supports validation and qualification activities within the manufacturing area. Ensures timely execution of Environmental Monitoring sampling responsibilities. Supports annual requalification programs and area readiness activities. Provides assistance to other manufacturing areas as operational needs arise. Communicates status of documentation, activities, and pending actions to supervision and partner departments. Ensure Safety, Environmental, and GMP Compliance Executes all activities with a strong focus on employee safety, environmental protection, contamination control, and compliance with cGMP standards. Maintains housekeeping and aseptic conditions within controlled environments in alignment with contamination‑control practices. Handles hazardous and non‑hazardous waste according to Environmental, Health & Safety (EHS) procedures. Completes required training for cGMP, EHS, aseptic practices, and company policies. Actively identifies and reports safety risks, participating in initiatives to promote a safe and compliant work environment. Requires steady attention to detail during routine manufacturing tasks such as equipment setup, monitoring processes, and completing documentation. Must maintain awareness of process conditions, noticing alarms, unusual readings, or equipment irregularities and escalating them promptly. Requires regular use of digital systems and control screens, needing accurate visual checks and basic interpretation of displayed information. Must stay focused during repetitive tasks and when working inside controlled areas or around production equipment. Requires the ability to remain calm and attentive when unexpected situations arise, such as abnormal process conditions or minor deviations. Identify and promptly report inconsistencies, atypical conditions, or potential violations of company procedures, quality requirements, or safety policies to supervision. Plans and organize work activities with a sense of urgency, adjusting priorities to meet operational deadlines in a dynamic and rapidly changing manufacturing environment. Applies sound judgment to resolve routine operational issues, escalating when appropriate to ensure safe and compliant operations. Proposes alternatives and evaluates risks and benefits when supporting process decisions, aligning personal and team activities with departmental objectives, business priorities, and BMS values. #BMSBL We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. C