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.
Reporting to the Shift Manager, Production Engineer/Scientist 1 of the Single Use Facility is responsible for advancing the biologics pipeline according to established work instructions and in accordance with current Good Manufacturing Practices (cGMPs). The role is based in a state of the art facility utilizing single-use technology.
The Production Engineer/Scientist 1 is responsible for mastering all routine manufacturing assignments/processes, providing daily technical oversight of execution of manufacturing processes, provide in depth training, maintaining a culture of compliance, and innovation within the downstream team. The Production Engineer/Scientist 1 is required to guide the shift personnel with technical knowledge to lead troubleshooting activities, provide investigation support, analyze process/equipment data, and identify and implement process improvements.
Key Responsibilities:
Master and work on routine manufacturing assignments as well as assignments that are complex in nature where action and a high degree of initiative are required in resolving problems and making recommendations
Provide in depth training
In adherence to Good Manufacturing Practices and standard operating procedures effectively use and possesses mastery of various production equipment, process automation, and supporting business systems to support biologics production within the downstream operations
Ensure less experienced manufacturing personnel comply with Standard Operating Procedures (SOPs) and work instructions and work with individual team members to ensure training is completed on time
Under direction of area management, lead the coordination and implementation of special projects such as validation or support routine process investigations
Actively participate in tech transfers
Revise and create process documents
Champion areas specific initiatives associated with work safety and operational improvements
Engage in and support culture of continuous improvement through ownership of improvement for work processes, equipment and safe work environment
Advise Shift manager on improvements which may optimize work processes
Qualifications & Experience:
Bachelor’s degree in Engineering (Chemical, Mechanical, Industrial, Biomedical Engineering) or Life Sciences (Chemistry, Biochemistry, Microbiology) with 0+ years’ experience
Knowledge of science generally attained through a degree in the STEM fields
Strong academic performance
Passion for science and a strong interest in manufacturing operations as a career
Fast learner with strong scientific curiosity, good interpersonal skills, and attention to detail
Previous internships/co-op in pharma and/or research experience at university
Excellent and oral communication skills
Demonstrated leadership in professional, school, or community settings
Demonstrated proficiency in common computer tools and web based applications
Prior experience successfully participating on work teams where personal accountability, attention to detail, collaboration, and results were expected
#LI-Onsite #BMSBLDMA
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
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 [email protected]. 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.
