Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Position Summary

Senior Technician within Clinical Trials Packaging and Labelling operations, working to a high standard with increased independence to deliver safe, compliant, right-first-time execution of clinical supply activities.

• Demonstrate strong working knowledge of approved SOPs, Work Instructions, batch records, electronic systems and GMP requirements, supporting timely completion of process orders and escalation of issues
• Act as an experienced operational contributor by supporting problem solving, process discipline, continuous improvement, and the development of less experienced technicians.

Key Responsibilities

• Maintain high standards of cGMP, safety, documentation, data integrity and good housekeeping practices, actively identifying and escalating risks or abnormal conditions.
• Completion of Primary and Secondary production operations in accordance with approved procedures.
• Operate GMP equipment to support production, including set-up, in-process checks, basic troubleshooting, post-operation strip down and cleaning.
• Complete electronic batch records, equipment logbooks and associated production documentation accurately and in a timely manner, including relevant SAP transactions.
• Demonstrate the ability to work independently or as part of a team across general production operations and supporting tasks
• Monitor production processes and equipment performance, resolve routine issues within training and authority, and escalate non-routine issues appropriately.
• Apply a good working understanding of regulatory, GMP, safety and quality requirements relevant to clinical trial packaging and labelling, including when to stop, challenge or escalate work.
• Support investigations, deviation assessment, root cause analysis, corrective actions and change control activities where required, providing accurate operational input and evidence.
• Participate in internal audits, inspections, readiness activities, equipment validation or system user acceptance testing
• Support continuous improvement by identifying opportunities to improve workflow, compliance, safety, quality, material flow or operational efficiency.
• Support training, coaching and mentoring of technicians by sharing technical knowledge, reinforcing procedural discipline and helping embed good GMP behaviours.
• Contribute to a respectful, inclusive and collaborative team environment, modelling accountability, clear communication and patient-focused decision making.
• Demonstrate a patient-focused mindset by recognising the importance of clinical supply activities to trial delivery, product quality and patient outcomes.