Manufacturing Associate, CAR-T

Bristol Myers Squibb•Summit, NJ

19h•Onsite

About The Position

Bristol Myers Squibb is reimagining the future of cell therapy and is seeking a Manufacturing Associate, CAR-T to join their team. This role involves manufacturing human blood-derived components in a controlled, cGMP cleanroom environment, adhering to strict regulatory requirements and Standard Operating Procedures. The position is part of a team working on a specific production shift schedule, requiring communication of deviations and assistance with quality investigations. The company emphasizes challenging and meaningful work that transforms patients' lives and offers opportunities for professional growth and development within a supportive culture.

Requirements

Knowledge of cGMP/FDA regulated industry
Basic mathematical skills
General understanding of cGMPs
Technical writing capability
Proficient in MS Office applications
Inventory control and/or management
Background to include an understanding of biology, chemistry, medical or clinical practices
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.

Responsibilities

Create inclusive culture that builds relationships with support groups
Execute operations as outlined in Source Governing Documents (including but not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms)
Executes transactions and process in all electronic systems and adheres to business continuity processes
Prioritizes safety of self and others
Reports safety events within 24 hours
Immediately escalates any/all issues that may impact compliance or safety of self and/or others
Complete documentation required by Source Governing Documents contemporaneously
Perform all tasks in a manner consistent with the safety policies, SOPs, quality systems, and GMP requirements including ALCOA+
Complete training assignments prior to assigned due date to ensure necessary technical skills and knowledge
Train for proficiency in process systems and some supporting business systems
Execute the daily unit operations schedule, that includes people, product, and material flow across multiple shifts
Work within a control cleanroom environment and execute aseptic processing procedures (as assigned)
Maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements
Continues to refine and improve manufacturing process technique to improve individual operational times
Verifies training completion prior to performing any GxP tasks
Author Manufacturing operating procedures that are technically sound, promote effective and efficient operations and comply with cGMP requirements

Benefits

Medical, pharmacy, dental, and vision care.
BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)) for US Exempt Employees.
160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays for Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees.
Unlimited paid sick time
Up to 2 paid volunteer days per year
Summer hours flexibility
Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs
Annual Global Shutdown between Christmas and New Years Day.