Bristol Myers Squibb
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Senior Manager, GMP Facilities
role at
Bristol Myers Squibb
4 days ago Be among the first 25 applicants
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: careers.bms.com/working-with-us.
At 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.
Shift Available Monday - Friday, Onsite Day Shift, 7:30 a.m. - 4 p.m.
Responsibilities
Member of the Site Safety Committee.
Champions safety and compliance as a leader within the Facilities & Engineering Department. Set expectations and ensure adherence to Safety and Environmental regulations, Good Manufacturing Practices, Governing Building Codes, and other applicable industry regulations related to the manufacture of pharmaceutical products. Ensure that the right support structure is in place to facilitate compliance with those requirements. Supports the development of related procedures and programs, implement and monitor performance. Identifies areas of opportunity and prepares specific action plans to increase awareness and to maintain compliance.
Set short- and long-term strategies for the team that aligns with Facilities & Engineering and Summit West Cell Therapy objectives. Communicate a clear vision for the team aligned with the Summit West and overall business objectives.
Develop and manage the team through hiring, talent development, coaching, and performance management in a manner that creates an inclusive and supportive work environment.
Develop and implement systems and processes that minimize inconsistencies or defects in equipment that could lead to variability in equipment/system output.
Implement and track best in class maintenance and reliability KPI's and ensure the appropriate review process is in place so actions are being taken to address performance issues.
In collaboration with Reliability, define and implement strategies to ensure that equipment is operating reliably and per design specifications.
Identify opportunities to implement and utilize predictive analytics (including machine learning where applicable) to improve equipment uptime and availability.
Implement and maintain inspection readiness programs to ensure that the critical utilities and facilities are always inspection-ready and maintained to the highest standards.
Maintain a collaborative and positive working relationship with our Integrated Facilities Management service provider and direct managed third-party providers to deliver best in class facilities support services.
Champion Safety by partnering with site and corporate EHS to develop and implement processes, procedures, and strategies to ensure that we are creating an environment and culture to keep our employees safe.
Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while maintaining highly compliant facilities.
Broad knowledge of Good Manufacturing Practices, Building Codes, OSHA regulations, and Industry Regulations related to the manufacture of pharmaceutical products.
Develops relationships with diverse groups across the client base at the Summit West site. Work within a team environment with other Site Engineering functions, including Plant Engineering in a matrix organization.
Ability to build and sustain strong relationships with internal and external stakeholders including Manufacturing, Quality, EHS, and local community and regulatory agencies to meet site and business requirements.
Develops and monitors key performance indicators for utility operations. Drives appropriate actions to mitigate performance issues.
Knowledge & Skills
Experience managing the operations and maintenance of critical utilities supporting a manufacturing operation.
Experience with Quality Management Systems, specifically Change Control.
Experience interacting with regulatory agencies and local government officials.
Mastery of a technical function such as metrology or automation as well as pharmaceutical processes such as building systems, manufacturing operations, etc.
Specific knowledge of equipment reliability principles and processes as related to maintenance best practices.
Knowledge and experience in supporting cell therapy processes.
Knowledge and experience in the maintenance and operation of clean utilities such as clean room HVAC systems and Building Management Systems within a GMP manufacturing facility.
Working knowledge and experience with regulatory inspections preferably as an SME lead.
Fundamental understanding of the maintenance principles and requirements for electrical, HVAC, process heating and cooling utilities.
Experience leading a large team of multi-skilled trades within a regulated manufacturing environment.
Experience managing OPEX and/or CAPEX budgets.
Ability to manage or be an active team member of cross-functional project teams.
Must have a BA degree in Facilities Management, Engineering, OR equivalent experience.
Knowledge of BMS business objectives, strategies, and the pharmaceutical industry.
Understanding of regulatory, environmental, GMP, GLP and OSHA regulations.
Minimum Requirements
Bachelor's degree in a technical field, preferably Engineering. An equivalent amount of education, certifications and experience to be considered.
Minimum 10 years pharmaceutical industry experience with specific expertise in facilities type role responsible for the critical utilities systems supporting pharmaceutical or biotech manufacturing operations.
Minimum of 3 years' experience leading an Engineering and/or Facilities Team.
Compensation Overview Summit West - NJ - US: $125,740 - $152,368
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Supports People With Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Additional Information If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Senior Manager, GMP Facilities
role at
Bristol Myers Squibb
4 days ago Be among the first 25 applicants
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: careers.bms.com/working-with-us.
At 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.
Shift Available Monday - Friday, Onsite Day Shift, 7:30 a.m. - 4 p.m.
Responsibilities
Member of the Site Safety Committee.
Champions safety and compliance as a leader within the Facilities & Engineering Department. Set expectations and ensure adherence to Safety and Environmental regulations, Good Manufacturing Practices, Governing Building Codes, and other applicable industry regulations related to the manufacture of pharmaceutical products. Ensure that the right support structure is in place to facilitate compliance with those requirements. Supports the development of related procedures and programs, implement and monitor performance. Identifies areas of opportunity and prepares specific action plans to increase awareness and to maintain compliance.
Set short- and long-term strategies for the team that aligns with Facilities & Engineering and Summit West Cell Therapy objectives. Communicate a clear vision for the team aligned with the Summit West and overall business objectives.
Develop and manage the team through hiring, talent development, coaching, and performance management in a manner that creates an inclusive and supportive work environment.
Develop and implement systems and processes that minimize inconsistencies or defects in equipment that could lead to variability in equipment/system output.
Implement and track best in class maintenance and reliability KPI's and ensure the appropriate review process is in place so actions are being taken to address performance issues.
In collaboration with Reliability, define and implement strategies to ensure that equipment is operating reliably and per design specifications.
Identify opportunities to implement and utilize predictive analytics (including machine learning where applicable) to improve equipment uptime and availability.
Implement and maintain inspection readiness programs to ensure that the critical utilities and facilities are always inspection-ready and maintained to the highest standards.
Maintain a collaborative and positive working relationship with our Integrated Facilities Management service provider and direct managed third-party providers to deliver best in class facilities support services.
Champion Safety by partnering with site and corporate EHS to develop and implement processes, procedures, and strategies to ensure that we are creating an environment and culture to keep our employees safe.
Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while maintaining highly compliant facilities.
Broad knowledge of Good Manufacturing Practices, Building Codes, OSHA regulations, and Industry Regulations related to the manufacture of pharmaceutical products.
Develops relationships with diverse groups across the client base at the Summit West site. Work within a team environment with other Site Engineering functions, including Plant Engineering in a matrix organization.
Ability to build and sustain strong relationships with internal and external stakeholders including Manufacturing, Quality, EHS, and local community and regulatory agencies to meet site and business requirements.
Develops and monitors key performance indicators for utility operations. Drives appropriate actions to mitigate performance issues.
Knowledge & Skills
Experience managing the operations and maintenance of critical utilities supporting a manufacturing operation.
Experience with Quality Management Systems, specifically Change Control.
Experience interacting with regulatory agencies and local government officials.
Mastery of a technical function such as metrology or automation as well as pharmaceutical processes such as building systems, manufacturing operations, etc.
Specific knowledge of equipment reliability principles and processes as related to maintenance best practices.
Knowledge and experience in supporting cell therapy processes.
Knowledge and experience in the maintenance and operation of clean utilities such as clean room HVAC systems and Building Management Systems within a GMP manufacturing facility.
Working knowledge and experience with regulatory inspections preferably as an SME lead.
Fundamental understanding of the maintenance principles and requirements for electrical, HVAC, process heating and cooling utilities.
Experience leading a large team of multi-skilled trades within a regulated manufacturing environment.
Experience managing OPEX and/or CAPEX budgets.
Ability to manage or be an active team member of cross-functional project teams.
Must have a BA degree in Facilities Management, Engineering, OR equivalent experience.
Knowledge of BMS business objectives, strategies, and the pharmaceutical industry.
Understanding of regulatory, environmental, GMP, GLP and OSHA regulations.
Minimum Requirements
Bachelor's degree in a technical field, preferably Engineering. An equivalent amount of education, certifications and experience to be considered.
Minimum 10 years pharmaceutical industry experience with specific expertise in facilities type role responsible for the critical utilities systems supporting pharmaceutical or biotech manufacturing operations.
Minimum of 3 years' experience leading an Engineering and/or Facilities Team.
Compensation Overview Summit West - NJ - US: $125,740 - $152,368
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Supports People With Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Additional Information If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr