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 .

　　Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today. With therapies only in their infancy and BMS’s continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible.

　　Manufacture cell culture media preparation in support of S12 CAR T manufacturing per Standard Operating Procedures (SOPs) in a controlled, cleanroom environment.

　　Shifts Available:

　　This position is for Quad 1 Sunday to Tuesday, with every other Wednesday, from 6:00 am to 6:30 pmResponsibilities:

　　Perform set-up and operation of equipment to support production of media and solution preparation to support cell culture processes.

　　Aseptic technique is required for most activities: welding, connections, and transfers, at minimum. Aseptic qualification and gowning is required.

　　Perform activities in biological safety cabinets.

　　Support deviation investigations and write ups as needed. Support on time closure of any assigned CAPAs within the designated shift.

　　Weighs, calculates, and measures in-process materials to ensure proper quantities are added/removed.

　　Adheres to the production schedule ensuring on-time, internal production logistics.

　　Records production data and information in a clear and concise format according to proper GDPs, adhering to ALCOA+ principles.

　　Perform all tasks in a manner consistent with site safety policies, quality systems, and GMP requirements.

　　Works in a team based, cross-functional environment to complete production tasks required by shift schedule.

　　Motivated, team consciousness individuals are needed to fulfill job requirements.

　　Become a SME and qualified trainer within a designated function of manufacturing. Supervision will be managed by the shift Supervisor or designated Team Lead.

　　Maintain on time completion of training assignments to maintain the necessary technical skills and process knowledge.

　　Performs other tasks as assigned: continuous improvement projects, inspection readiness, right first-time initiatives, etc.

　　Knowledge & Skills:

　　Understanding of media and buffer preparation requirements for cell culture, and aseptic processing or lab techniques.

　　Familiarity with cGMP/FDA regulated industry.

　　Basic mathematical skills.

　　Ability to read, execute and document steps in a GMP batch record.

　　Proficient in MS Office applications.

　　Background to include a basic understanding of biology, chemistry, or pharmaceutical processing.

　　Pre-requisites: Prior experience in Manufacturing and/or scientific/engineering education

　　Basic Requirements:

　　Bachelor Degree

　　OR Associate / Medical Technical degree and 2 years of Manufacturing or Operations experience

　　OR HS Diploma / GED and 3 years of Manufacturing or Operations experience

　　Working Conditions:

　　Intermittent walking and sitting to perform job functions; however, ability to sit or stand for extended periods of time may be necessary.

　　Must be comfortable working with contained human blood components.

　　Physical dexterity sufficient to use computers and documentation.

　　Sufficient vision and hearing capability to work in job environment.

　　Ability to lift 25 pounds.

　　Must have the ability to work around laboratories and controlled, enclosed, restricted areas.

　　Cleanroom garments and personal protective equipment will be required in designated areas which cover head, parts of the face, core body, and legs/feet.

　　Makeup, gum, nail polish, or other potential microbial sources are prohibited in restricted areas.

　　Flexibility to don clean room garments and personal protective equipment (PPE).

　　Clean room environment is an enclosed, restricted space, with assigned pressure and temperature conditions. Reagents, chemicals, and exposure to sanitization agents are expected.

　　Routine exposure to human blood components. Exposure to strong magnets is likely.

　　Designated areas may prohibit food, any outside materials such as cell phones, tablets, at a minimum.

　　This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

　　This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

　　If you want to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here with our Cell Therapy team. Full of incredible and dedicated team members, those working on CAR-T and other forms of Cell Therapy are transforming patients’ lives through science. From studying individualized cell lines to making brand new discoveries, this bold and personal discipline allows you to grow your career while making a lasting impact on the field of medicine. Join us today.

　　BMSCART

　　#LI-ONSITE

　　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/ (https://careers.bms.com/eeo-accessibility) 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.

　　Company: Bristol Myers Squibb

　　Req Number: R1577784

　　Updated: 2024-01-18 23:06:31.013 UTC

　　Location: Summit,New Jersey

　　Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.