Manufacturing Associate, CAR T Media and Solution Preparation, Manufacturing Operations

Bristol-Myers Squibb; Summit (NJ); On-site; USD 40,000 - 80,000; Full time

Job summary

An innovative company is seeking a Manufacturing Associate to join their Cell Therapy team. This role involves working in a cleanroom environment to manufacture human blood-derived components, ensuring adherence to strict regulatory standards. You'll play a critical part in transforming patient lives through advanced cell therapy techniques. The position offers a unique opportunity for growth and development within a supportive team, where your contributions directly impact the future of healthcare. If you're passionate about science and eager to make a difference, this is the perfect opportunity for you.

Benefits

Competitive benefits

Flexible work environment

Opportunities for growth

Support for work-life balance

Qualifications

• Understanding of cell culture and aseptic processing techniques.
• Knowledge of cGMP/FDA regulations and quality systems.

Responsibilities

• Set up and operate equipment for blood component production.
• Support deviation investigations and maintain production logs.

Skills

Cell culture

Cryopreservation

Aseptic processing

Technical writing

Basic mathematics

MS Office proficiency

Education

Bachelor’s degree

Associate/Medical Technical degree

High School diploma/GED

Job description

Manufacturing Associate, CAR T Media and Solution Preparation, Manufacturing Operations

Apply locations Summit West - NJ - US | time type Full time | posted on Posted 3 Days Ago | job requisition id R1590883

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.

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.

Role Description

Our Manufacturing Associate, Cell Therapy team manufactures human blood derived components per Batch Record and Standard Operating Procedures in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable.

Shift Details

• Quad 4: Wednesday - Saturday (with e/o Wednesday off), Onsite Overnight Shift, 5 p.m. - 5:30 a.m.

*Start and end times are subject to change based on business demands.

Responsibilities

• Perform set-up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.
• Support deviation investigations and write ups as needed. Support on time closure of any assigned CAPAs within the designated shift.
• Aseptic technique is required for tube most activities: welding, connections, and transfers, at minimum. Aseptic qualification is required.
• Weighs 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, concise, format according to proper GDPs.
• 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-conscious 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.
• Perform other tasks as assigned: continuous improvement projects, inspection readiness, right first-time initiatives, etc.

Knowledge & Skills

• Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique.
• Knowledge of cGMP/FDA regulated industry.
• Basic mathematical skills.
• General understanding of cGMPs.
• Technical writing capability.
• Proficient in MS Office applications.
• Background to include an understanding of biology, chemistry, medical or clinical practices.

Basic Requirements

• Bachelor’s degree and no prior Manufacturing Operations experience.
• Or Associate/ Medical Technical degree and 2 years of Manufacturing Operations experience.
• Or High School diploma/GED and 4 years of Manufacturing or Operations experience.

Working Conditions

• Intermittent walking, standing and sitting to perform job functions; ability to stand for extended periods 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 the environment.
• Ability to lift 25 pounds.
• Must work in laboratories and controlled, enclosed, restricted areas.
• Cleanroom garments and PPE are required in designated areas.
• Prohibited items in restricted areas include makeup, gum, nail polish, perfume/cologne, and other potential microbial sources.
• Flexibility to don clean room garments and PPE.
• Work in a cleanroom environment with specific pressure and temperature conditions.
• Exposure to reagents, chemicals, sanitization agents, and human blood components.
• Restricted areas prohibit food and outside materials like cell phones and tablets.

BMSCART, #LI-Onsite

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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.

Our Culture and Additional Information

With a vision to “Transforming patients’ lives through science,” every BMS employee plays an integral role in work that goes far beyond ordinary. We promote a culture of passion, innovation, urgency, accountability, inclusion, and integrity. Our occupancy structure includes site-essential, site-by-design, field-based, and remote jobs, with specific requirements for onsite presence. We support accessibility and reasonable accommodations for applicants with disabilities. We encourage vaccination against Covid-19 and boosters. Qualified applicants with arrest and conviction records will be considered. For residents of Los Angeles County, additional info is available at https://careers.bms.com/california-residents/.