Specialist, Car-t Production Planning and Scheduling - Summit, United States - Bristol-Myers Squibb

Bristol-Myers Squibb

Verified Company

Summit, United States

1 week ago

Posted by:

Mark Lane

beBee recruiter

Description

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.

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.

Shifts Available:

5am 3:30pm Sunday to Wednesday
OR
12pm 10:30pm Wednesday to Saturday
Hours flexible and/or may change.

Responsibilities:

Create and maintain detailed site plans for operations including apheresis/PBMC receipt, material kitting, process intermediates, manufacturing, and drug product shipments
Point of contact for the Manufacturing Operations team to provide support, facilitating operational continuity and addressing issues as they arise.
Monitor and report KPI's to department leadership
Work with the Systems and Technology, Manufacturing Sciences and Technology team on system implementations and continuous improvement projects.
Collaborate with IT Business Partners in support of modeling and scheduling simulation implementations
Support the S&OP process by providing site level manufacturing capacities and operational capabilities
Maintain and update site procedures for CAR-T material management functions.
Performs other tasks as assigned.

Knowledge & Skills:

Understanding of cell culture, cryopreservation, purification, and aseptic processing or lab techniques.
Knowledge of cGMP/Pharmaceutical regulations.
Understanding of capacity planning, ERP systems and analytics/reporting tools.
Proficient written and verbal communication skills.
Proficient presentation development and delivery skills.
Technical writing capability.
Ability to work independently for extended periods of time.
Ability to work as part of a team.
Ability to develop and provide training on various functions.
Ability to creatively solve both routine and complex problems.
Ability to provide oncall support in case of emergent issues.
Ability to travel < 10% of time.

Basic Requirements:

Bachelor's degree required.
3+ years relevant work experience required, preferably in a regulated pharmaceutical manufacturing environment.

Preferred Requirements:

1+ years of experience supporting ERP systems (preferably Oracle EBS).
An equivalent combination of education, experience and training may substitute.

Working Conditions:

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.

Intermittent walking and sitting to perform job functions; however, ability to sit or stand for extended periods of time may be necessary.
Physical dexterity sufficient to use computers and documentation.
Sufficient vision and hearing capability to work in job environment.
Ability to lift up to 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.
Designated areas may prohibit food, any outside materials such as cell phones, tablets, at a minimum.

BMSCART

VETERAN
LI-ONSITE

Uniquely Interesting Work, Life-changing Careers

On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes