×
Register Here to Apply for Jobs or Post Jobs. X

Manager, Cell Therapy Manufacturing in Devens, MA Devens - MA - US R1601453 Posted ago

Job in Springfield, Hampden County, Massachusetts, 01119, USA
Listing for: Bristol-Myers Squibb
Part Time position
Listed on 2026-07-05
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 104975 - 127205 USD Yearly USD 104975.00 127205.00 YEAR
Job Description & How to Apply Below
Position: Manager, Cell Therapy Manufacturing in Devens, MA Devens - MA - US R1601453 Posted 21 hours ago
## Manager, Cell Therapy Manufacturing in Devens, MADevens - 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
** Manager, Cell Therapy Manufacturing
** supports the commercial operations  of the facility. The Manager will be responsible for the people manufacturing  both clinical and commercial product with oversight of shifts that cover 24/7 cell therapy manufacturing unit operations such as media preparation, cell  selection, cell processing, or product fill, all of which are executed in  accordance with Current Good Manufacturing Practices (cGMP’s).
** Shifts Available:
** TBD
* * Responsibilities:
*** Supporting the development, implementation and compliance of manufacturing documentation, procedures, & policies.
* Operating within the requirements of a validated manufacturing systems, plan, assign and oversee daily operational activities associated with assigned areas of responsibility.
* Maintaining operating and storage areas that are compliant, efficient, effective and safe.
* Identifying strategic and operational issues to prevent deviations and maintain a compliant environment. Leading and managing the development of corrective and preventative actions, deviation responses and investigations.
* Create an environment of teamwork, open communication, and a sense of urgency. Foster a culture of safety and compliance that embraces safety in the work environment and the safety of the patients by compliance with company procedures and policies, and cGMP requirements.
* Efficiently coordinating, communicating, and providing Operations project information and activities status to Planning, Manufacturing, Quality Assurance / Operations, Global Supply and other associated functions in a timely manner in accordance to schedules and defined implementation timelines
* Oversee operators on daily basis as they:  + Perform unit operations and support operations described in standard operating procedures and batch records in a safe and GMP compliant manner.  + Complete documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.  + Maintain training assignments to ensure the necessary technical skills and knowledge.  + Assist in the setup of manufacturing areas and equipment/fixtures and perform facility and equipment commissioning, qualification and validation activities.  

+ Writing manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements
* Hiring, mentoring and developing exceptional people
* Conducting performance reviews and identifying opportunities for career growth for manufacturing associates.
*
* Working Conditions:

*** This position will require shift work, including holidays and weekends
* This position will require you to work in a clean room…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary