Bristol Myers Squibb
Specialist, Associate Operations Engineer, Cell Therapy in Devens, MA
Bristol Myers Squibb, Harvard, Massachusetts, us, 01451
Specialist, Associate Operations Engineer, Cell Therapy
Location: Devens, MA
Working with Us
Challenging. Meaningful. Life‑changing. Working at Bristol Myers Squibb is anything but typical. Here, uniquely interesting work happens every day, from optimizing a production line to breakthroughs in cell therapy. The culture supports growth and recognizes the impact we have on patients’ lives. We offer competitive benefits and a flexible work environment designed to support both professional and personal goals.
Associate Operations Process Engineer, Cell Therapy
The associate provides technical support to the Devens Cell Therapy Facility manufacturing processes in a GMP environment. Responsibilities include troubleshooting process and equipment issues, collaborating with manufacturing and quality teams, implementing corrective actions, supporting process transfer and change control, and driving continuous improvement.
Shifts Available
Day Shift: 6 am – 6 pm (rotating schedule, including holidays and weekends)
Night Shift: 6 pm – 6 am (rotating schedule, including holidays and weekends)
Responsibilities
Provide on‑floor and on‑site troubleshooting and technical support for manufacturing and patient increase campaigns across variable shifts.
Facilitate deviation prevention and closure through site quality systems.
Analyze and summarize manufacturing data to support impact assessments and investigations.
Own change controls for routine process and procedure changes.
Own CAPA for manufacturing improvements.
Author and revise manufacturing SOPs and provide technical content for electronic batch records.
Participate in technology transfer for new processes and product implementation.
Train GMP operators on new procedures, processes, and changes.
Apply continuous improvement tools to identify and close procedural and compliance gaps.
Identify opportunities for process improvements and operational efficiencies and lead implementation efforts.
Interface with functions such as Scheduling, Global MSAT, Supply Chain, Quality, and Facilities & Engineering.
Support equipment and systems validation activities, including review of qualification documents, drafting user requirements, and participating in impact assessments.
Perform gowning activities and enter the manufacturing plant; exposure to strong magnetic fields is common.
Basic Requirements
BSc and/or MSc degree in Science or Chemical/Biological Engineering.
Minimum of 1 year of industry experience; cGMP and/or cell therapy manufacturing experience preferred.
Compensation Overview Devens, MA – $43.84 to $53.12 per hour. Additional incentive cash and stock options may be available.
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Working with Us
Challenging. Meaningful. Life‑changing. Working at Bristol Myers Squibb is anything but typical. Here, uniquely interesting work happens every day, from optimizing a production line to breakthroughs in cell therapy. The culture supports growth and recognizes the impact we have on patients’ lives. We offer competitive benefits and a flexible work environment designed to support both professional and personal goals.
Associate Operations Process Engineer, Cell Therapy
The associate provides technical support to the Devens Cell Therapy Facility manufacturing processes in a GMP environment. Responsibilities include troubleshooting process and equipment issues, collaborating with manufacturing and quality teams, implementing corrective actions, supporting process transfer and change control, and driving continuous improvement.
Shifts Available
Day Shift: 6 am – 6 pm (rotating schedule, including holidays and weekends)
Night Shift: 6 pm – 6 am (rotating schedule, including holidays and weekends)
Responsibilities
Provide on‑floor and on‑site troubleshooting and technical support for manufacturing and patient increase campaigns across variable shifts.
Facilitate deviation prevention and closure through site quality systems.
Analyze and summarize manufacturing data to support impact assessments and investigations.
Own change controls for routine process and procedure changes.
Own CAPA for manufacturing improvements.
Author and revise manufacturing SOPs and provide technical content for electronic batch records.
Participate in technology transfer for new processes and product implementation.
Train GMP operators on new procedures, processes, and changes.
Apply continuous improvement tools to identify and close procedural and compliance gaps.
Identify opportunities for process improvements and operational efficiencies and lead implementation efforts.
Interface with functions such as Scheduling, Global MSAT, Supply Chain, Quality, and Facilities & Engineering.
Support equipment and systems validation activities, including review of qualification documents, drafting user requirements, and participating in impact assessments.
Perform gowning activities and enter the manufacturing plant; exposure to strong magnetic fields is common.
Basic Requirements
BSc and/or MSc degree in Science or Chemical/Biological Engineering.
Minimum of 1 year of industry experience; cGMP and/or cell therapy manufacturing experience preferred.
Compensation Overview Devens, MA – $43.84 to $53.12 per hour. Additional incentive cash and stock options may be available.
#J-18808-Ljbffr