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Job Details

Sr. Manufacturing Associate CAR T

Location
Summit, NJ, United States

Posted on
Jun 16, 2020

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Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

PURPOSE AND SCOPE OF POSITION:

Manufactures human blood derived components per Standard Operating Procedures (SOPs) 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. This position is for the Weekend Shift Friday, Saturday, Sunday. Weekend Day shift coverage is 7 am to 7:30 pm, Weekend night Shift Coverage is from 7 pm to 7:30 am. Start and end times are subject to change based on business demands.

This position is a member of the Manufacturing Operations organization.

DUTIES AND RESPONSIBILITIES:


Production of blood component lots through cell culture, harvest, and cryopreservation.
Aseptic technique and operations connections, tubing welding, transfers may be performed in a Biological Safety Cabinet (
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.
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.
Leads a team within a designated function of manufacturing, however, supervision will be managed by the shift Supervisor.
No direct reports will be assigned to this job role.
Performs other tasks as assigned.


REQUIRED COMPETENCIES:

Knowledge, Skills, and Abilities:


Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique
Aseptic technique is required for tube most activities: welding, connections, and transfers, at minimum.
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
Sufficient vision and hearing capability to work in job environment.
Entry- Level


Education and Experience:

Bachelor's degree

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

or High School diploma/GED and 4 years of Manufacturing or Operations experience.

WORKING CONDITIONS (US Only):


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.
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.


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 the resources to pursue their goals, both at work and in their personal lives.

Company: Bristol-Myers Squibb

Req Number: R1526521_EN

Updated: 2020-06-15 00:00:00.000 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.

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