CSO Technician

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. Bristol Myers Squibb recognises the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programmes that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Join our dynamic team as a Clinical Supplies Technician, where your passion for quality, attention to detail and customer service will drive the advancement of critical healthcare solutions. In this pivotal role, you will be working in a team to produce clinical trial kits within a GMP-regulated environment, ensuring precision and compliance in clinical trial packaging. As a vital team member, you will have the opportunity to collaborate on projects, fostering innovation and excellence in everything you do.

• Start-up, execute, cleaning and completion of clinical trial packaging operations in accordance with appropriate Standard Operating Procedures.
• Primary packaging (bottle filling) of oral dosage forms using a range of equipment.
• Labelling and assembly of clinical trials supplies, including automated labelling and walleting equipment.
• Working independently and as part of a team, on equipment or process projects.
• Control and monitor production process and equipment; resolve problems or correct abnormal conditions, conduct basic troubleshooting, and escalate problems appropriately.
• Develop and apply a working knowledge of relevant electronic systems, including SAP.
• Complete electronic batch documentation, equipment logbooks and other documentation relevant to all stages of production.
• Understand and follow GMP requirements and defined procedures to maintain the requirements of quality standards in the packaging environment.
• Work safely in the packaging environment, understanding personal responsibility for Health, Safety and the Environment and principles of risk management.
• Understand and comply with procedures relevant to COSHH.
• Participate in internal audits.
• Passionate about quality and customer service.
• Participate in continuous process improvement.

• Typically educated to A level standard, preferably in subjects relating to sciences or IT.
• Problem-solving skills and ability to work effectively with colleagues to resolve problems.
• Communication and interpersonal skills.
• Ability to work accurately to deadlines.
• Computer literate.
• Ability to develop and share knowledge.

• Experience of packaging and labelling environment in a GMP environment, preferably within clinical trials.
• Working knowledge in SAP.
• Basic knowledge of clinical trial operations.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

With a single vision as inspiring as “Transforming patients’ lives through science™”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.