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 Summary:
Join the Cell Therapy Technical Operations (CTTO) division and be a part of the team building leading cell therapy platforms to serve our patients with novel cellular immunotherapies. The Viral Vector Commercial Network Manufacturing Science and Technology (MS&T) group plays a critical role in technology transfers, process validation, CMC life cycle management, technical oversight of external manufacturing partners, process engineering and establishing manufacturing standards to enable a robust and scalable global cell therapy manufacturing network.
We are looking for a Senior/Principal Engineer to join our Viral Vector Commercial Network MS&T group. The key function of this role will be to provide commercial manufacturing support of our CMO GMP manufacturing facilities. Additionally, this position will be part of a team responsible for transferring commercial manufacturing processes and will play a key role in product lifecycle management including strategic development, validation, and approval of viral vector products. This person will collaborate cross-functionally to ensure project advancement, solutioning around challenges/opportunities, and rapid and best in class execution.
Key Responsibilities:
- Support all Manufacturing Sciences & Technologies (MSAT) activities at CMOs to ensure uninterrupted clinical/commercial vector manufacturing and supply
- Provide technical process support for routine clinical/commercial batches and assist QA with on time closure of all quality system records such as deviations, CAPAs and change controls
- Develop and manage tools/templates to monitor vector manufacturing process performance and enable understanding of process capability
- Implement and support the execution of process control strategies including execution of process risk assessments and CPV
- Ensure the manufacturing process is in a state of control through an understanding of CPV data
- Support production related investigations, determining the root cause and ensuring compliance with internal standards and regulatory requirements
- Support regulatory inspections and permanent inspection readiness
- Write technical reports in support of manufacturing process changes, deviation investigations and regulatory filings
- Develop and execute manufacturing process improvement activities in accordance with the overall life cycle plan for the product
- Share operational best practices and process learning with the rest of the manufacturing network
Qualifications & Experience:
- Biochemical, Chemical, Biomedical Engineering or Cell Biology/Immunology discipline with either a B.S. with a minimum of 6 years of relevant experience, a M.S with a minimum of 4 years of relevant experience, or a Ph.D. with a minimum of 2 years of relevant experience (Note: experience level will determine position title and enterprise grade level)
- Experience with technical support of a cGMP manufacturing facility, including strong knowledge and engineering leadership for viral vector manufacturing and processing equipment, manufacturing support, and technology transfer
- Flexibility to work within manufacturing schedules and ability to travel frequently (50%)
- Experience with cellular therapies is preferred
- Ability to work in a self-driven, performance/results oriented, fast-paced matrix environment
- Demonstrated strong written and verbal communication, interpersonal skills, presentation skills, time management skills, sense of urgency, attention to detail, teamwork, and cross-functional collaboration
- Proficiency utilizing MS Office products and working knowledge of statistical software (R, JMP, Minitab) strongly preferred
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 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.
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