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.

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'll 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'll have the opportunity collaborate on projects, fostering innovation and excellence in everything you do.

Key Responsibilities

Start-up, execute, cleaning and completion clinical trial packaging operations in accordance with appropriate Standard Operating Procedures.Primary packaging (bottle filling) of oral dosage forms using a range of equipmentLabelling and assembly of clinical trials supplies, including automated labelling and walleting equipmentWorking independently and as part of a team, on equipment or process projectsControl 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 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 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.

Required Skills and Qualifications

Typically educated to A level standard, preferably in subjects relating to sciences or ITProblem-solving skills and ability to work effectively with colleagues to resolve problemsCommunication and interpersonal skillsAbility to work accurately to deadlinesComputer literateAbility to develop and share knowledge

Required Knowledge and Experience

Experience of packaging and labelling environment in a GMP environment, preferably within clinical trials.Working knowledge in SAPBasic 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.

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 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.

On-site Protocol
BMS has an 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 adastaffingsupport@bms.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