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 rich in diversity. 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 Overview We are seeking a dynamic Supervisor to lead our experienced team in the packaging and labelling of clinical supplies. This role involves overseeing GMP, safety, and procedural aspects within a cGMP production area. If you have prior experience in the pharmaceutical industry, especially in clinical trials packaging, we want to hear from you Key Responsibilities Technical Expertise : Demonstrate a thorough understanding of cGMPs related to clinical supply packaging and labelling. Production Management : Review the master production schedule, establish priorities, and adjust schedules as needed to meet production order specifications. Team Supervision : Oversee staff in all aspects of packaging and labelling, and maintain employee records (attendance, vacation, etc.). Compliance Assurance : Ensure all production orders are executed in accordance with cGMPs and SOPs, utilizing SAP for accurate technical documentation. Continuous Improvement : Foster a work environment that supports continuous improvements aligned with the Company’s Quality Systems and procedures. Technical Writing : Generate COSHH, safety risk assessments, Data Integrity Risk Assessments, Quality Risk management Risk Assessments, procedures, and guidelines. Cross-Functional Interaction : Liaise with team members from Packaging & Labelling, Quality, Logistics, and Quality Control. Training Oversight : Conduct and oversee training for new and existing employees, ensuring training is up-to-date and documented. Health and Safety : Ensure adherence to health and safety guidelines. Problem Solving : Lead root cause investigations for process deviations and assign corrective/preventative actions. Key Skills Required Leadership Experience : Prior supervision of production staff or a leadership role within a production operation, with demonstrated ability in scheduling, organizing, and team building. Regulatory Knowledge : Working knowledge of cGMPs and regulatory requirements (MHRA, FDA, EU CTR, etc.) within a clinical packaging and labelling environment. Attention to Detail : Strong record of attention to detail and strict adherence to procedures and regulations. Pharmaceutical Knowledge : Good understanding of the pharmaceutical development process and associated scientific principles Packaging and labelling : solid understanding of both manual and automated packaging operations. Communication Skills : Ability to communicate effectively with various support groups and lead in a team environment. Adaptability : Effectively manage competing priorities, adapt to change, and accept additional responsibilities. Technical Proficiency : Working knowledge of MS Office, MS Outlook, and business software systems commonly used in the pharmaceutical industry (e.g., SAP, Veeva). Scheduling Ability : Demonstrated ability to effectively schedule multiple jobs/orders. Education and Experience Required Bachelor of Science or Mechanical Engineering Degree. Industry Experience : Demonstrated experience in the pharmaceutical industry. Preferred Experience : Experience in pharmaceutical manufacturing with a focus on the production of Clinical Trial Supplies. Leadership Experience : Extensive experience in progressive leadership or supervisory roles in the pharmaceutical industry. 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. Uniquely Interesting Work, Life-changing Careers 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 an inclusive culture, promoting diversity 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. On-site Protocol BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupportbms.com. Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Bristol Myers Squibb is Disability Confident – Employer A UK Government scheme