Supply Chain Operator, Cell Therapy Devens - MA - US R1603186 Posted

Position: Supply Chain Operator, Cell Therapy Devens - MA - US R1603186 Posted a day ago
## Supply Chain Operator, Cell Therapy Devens - MA - USFind out how well you match with this job
** 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:  
** 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.

The
** Supply Chain Operator, Cell Therapy
** brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The incumbent must be enthusiastic, innovative, goal-oriented, flexible, able to work efficiently with safety and quality in mind, and understand good manufacturing practices to support routine patient and/or healthy donor samples received, finished goods product labeling and packaging manufacturing operations, and finished goods product shipment for Cell Therapy.
** Shifts Available:
** Day

Shift: 6am - 6pm, rotational schedule including holidays and weekends
** Responsibilities will include, but are not limited to the following:
*** Performs cGMP functions associated with packaging operations, including visual inspection, labeling, and cartoning to support operations described in standard operating procedures and batch records.
* Performs receiving transitions for patient and/or healthy donor samples and shipments for finished goods product.
* Performs room sanitization activities to maintain controlled environment compliance.
* Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.
* Performing tasks consistently with the safety policies, quality systems, and GMP requirements.
* Completing training assignments to ensure the necessary technical skills and knowledge.
* Assisting in setting up packaging manufacturing areas and equipment/fixtures. Perform facility and equipment commissioning activities.
* Train others on SOPs, Work Instructions to successfully complete product packaging operations.
* Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts.
* Additional duties, tasks, and responsibilities as assigned by the Supply Chain department.
** Knowledge, Skills & Abilities:
*** Experience in electronic batch records preferred.
* Driven and motivated individual to learn and execute Final Product Packaging operations.
* Must have the ability to work assigned shift (Day or Night).
* Must have the ability to work flexible hours, including weekends and/or Holidays, to complete work activities.
* Must be able to work in a clean room environment and perform Final Product Packaging.
* Must be comfortable being exposed to human blood components.
* Must be able to work with temperature-controlled products.
* Receiving and Shipping experience a plus.
* Knowledge of inventory systems preferred.
* The ability to read, write and verbally communicate in English.
* Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is preferred.
*
* Minimum Requirements:

*** High school diploma and or GED…