NIGHT SHIFT Manager, Cell Therapy Manufacturing in Devens, MA

Devens, MA - USA

Monthly Salary: Not Disclosed

Posted on: 09-11-2025

Vacancies: 1 Vacancy

Job Summary

Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll 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 theres no better place than here at BMS with our Cell Therapy team.

BMS is seeking a Manager of Cell Therapy Manufacturing for a manufacturing facility in Devens MA. The Manager will support the start-up and commercial licensure of the Cell Therapy facility. This manager will be responsible for shifts that cover 24/7 cell therapy operations and will oversee manufacturing associates.

Shifts Available:

Night Shift: 6pm 6am rotating schedule including holidays and weekends

C Shift: Wed - Sat / Th - Sat 6pm - 6am including holidays and weekends

Responsibilities:

Manage the creation implementation and compliance for all documentation procedures and policies
Operate within the requirements of a validated manufacturing systems plan assign and oversee daily operational activities associated with assigned areas of responsibility.
Maintain operating and storage areas that are compliant efficient effective and safe.
Identify strategic and operational issues to prevent deviations and maintain a compliant environment. Lead and manage the development of corrective and preventative actions deviation responses and investigations.
Manage implementation and maintenance of appropriate training curricula
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 coordinate communicate and provide 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
Hire mentor and develop exceptional people: Conduct performance reviews and identify opportunities for career growth for manufacturing associates.
This position will require shift work including holidays and weekends.
This position will require you to work in a clean room environment with exposure to human blood components and in close proximity to strong magnets.

Knowledge and Skills:

Advanced ability to accurately and completely understand follow interpret and apply global regulatory and cGMP requirements.
Demonstrated advanced technical writing skills.
Advanced strategic thinking and problem-solving ability/mentality technically adept and logical.
Ability to work independently in a fast-paced team environment meet deadlines and prioritize work from multiple projects.
Advanced ability to communicate and collaborate effectively with peers senior management and cross-functional peers about task status roadblocks and needs locally and globally.
Advanced mentoring coaching influencing negotiating and personnel interaction skills.

Basic Requirements:

Bachelors in relevant science or engineering discipline or equivalent in work experience.
5 years of experience in cGMP biologics cell culture manufacturing
Experience in the following is highly preferred:
- Cell therapy manufacturing
- Aseptic processing in ISO 5 biosafety cabinets and universal precautions for handling human derived materials in BSL-2 containment areas.
- Cell expansion using incubators and single use bioreactors Cell washing processes Cell separation techniques and cryopreservation processes and equipment.

BMSCART

#LI-ONSITE

GPS2025

Working with UsChallenging. Meaningful. Life-changing. Those arent 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 breakthrou...

Shifts Available:

Night Shift: 6pm 6am rotating schedule including holidays and weekends

C Shift: Wed - Sat / Th - Sat 6pm - 6am including holidays and weekends

Responsibilities:

Manage the creation implementation and compliance for all documentation procedures and policies
Operate within the requirements of a validated manufacturing systems plan assign and oversee daily operational activities associated with assigned areas of responsibility.
Maintain operating and storage areas that are compliant efficient effective and safe.
Identify strategic and operational issues to prevent deviations and maintain a compliant environment. Lead and manage the development of corrective and preventative actions deviation responses and investigations.
Manage implementation and maintenance of appropriate training curricula
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 coordinate communicate and provide 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
Hire mentor and develop exceptional people: Conduct performance reviews and identify opportunities for career growth for manufacturing associates.
This position will require shift work including holidays and weekends.
This position will require you to work in a clean room environment with exposure to human blood components and in close proximity to strong magnets.

Knowledge and Skills:

Advanced ability to accurately and completely understand follow interpret and apply global regulatory and cGMP requirements.
Demonstrated advanced technical writing skills.
Advanced strategic thinking and problem-solving ability/mentality technically adept and logical.
Ability to work independently in a fast-paced team environment meet deadlines and prioritize work from multiple projects.
Advanced ability to communicate and collaborate effectively with peers senior management and cross-functional peers about task status roadblocks and needs locally and globally.
Advanced mentoring coaching influencing negotiating and personnel interaction skills.

Basic Requirements:

Bachelors in relevant science or engineering discipline or equivalent in work experience.
5 years of experience in cGMP biologics cell culture manufacturing
Experience in the following is highly preferred:
- Cell therapy manufacturing
- Aseptic processing in ISO 5 biosafety cabinets and universal precautions for handling human derived materials in BSL-2 containment areas.
- Cell expansion using incubators and single use bioreactors Cell washing processes Cell separation techniques and cryopreservation processes and equipment.

BMSCART

#LI-ONSITE

GPS2025

Key Skills

Restaurant Experience
Kitchen Experience
Inventory Control
Hospitality Experience
Dayforce
Lean Six Sigma
Management Experience
Facilities Management
Warehouse Experience
Supervising Experience
Restaurant Management
Commercial Cleaning

Apply Now

About Company

Bristol Myers Squibb

Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more

View Profile View Profile

AI AutoApply

Apply to 100+ jobs with one click