Senior Manager, Global Capital Project Delivery
Bristol-Myers Squibb
Senior Manager, Global Capital Project Delivery
Job Description
Lead the development of capital project scope, objectives, and delivery (from concept to validation and startup process) with emphasis on R&ED Laboratories and Chemical Development Projects in support of the business strategy concerning clients and stakeholders Drive effective project leadership, decision-making, and problem-solving through development of creative solutions as needed throughout lifecycle of projects Lead and promote effective teamwork by engaging both Facilities as well as key cross-functional clients and stakeholders to ensure appropriate internal and external resources are incorporated into the project design and execution Lead the scheduling, planning, control and effective coordination of all the parallel activities related to each project and maintain project schedule through minimal unanticipated schedule challenges Ensure that the construction project and the finished facility are compliant with all applicable safety, regulatory, legal requirements Achieve effective financial control through management of project scope, estimating, effective use of SAP, RPM, SRM, budget control tools, risk management, and project closeout Achieve high customer satisfaction by delivering finished projects on time that are fully commissioned, qualified and ready for startup/occupancy, and meet all requirements of stakeholders Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Bachelor's degree in Engineering (Chemical/Mechanical preferred). PMP certification & EIT/PE License a plus 8-12 years' experience managing pharmaceutical capital projects, especially with API and/or Pilot Plant Facilities Experience managing multiple complex EPCMV projects ($10M - $50M+) using the Stage Gate Process Demonstrated success leading multi-disciplinary and multi-functional teams and demonstrated strength in stakeholder management Experience with Process Hazard Analysis (PHA), Process Safety Management (PSM), and Pre-Startup Safety Review (PSSR) Understanding of financial management as it relates to capital and expense spending and project cash flow forecasting Hands-on experience in the negotiation and management of contracts and agreements with engineering contractors, vendors, regulatory and government agencies Extensive knowledge of working with the unionized workforce Understanding of regulatory, environmental, GMP and OSHA regulations, as well as functional requirements of pharmaceutical facilities, engineering best practices, design guidelines and standards, value engineering, closeout documentation standards, and life cycle costing Interpersonal and collaboration skills necessary to interface with and influence all levels of management Demonstrated Project Management expertise for design, construction, qualification, start-up, and tech transfer involving all areas of Pharmaceutical Manufacturing, Pilot Plants, and Research Facilities Experience interfacing with a variety of customers such as Manufacturing, Chemical Development, and Maintenance Excellent planning, organizing, analysis and problem-solving skills Proficient in Microsoft Excel, Project, PowerPoint, SAP, RPM (Project Capital System), SRM (Purchase Order System)
Key Responsibilities
- Lead the development of capital project scope, objectives, and delivery from concept to validation and startup process
- Drive effective project leadership, decision-making, and problem-solving through development of creative solutions
- Lead and promote effective teamwork by engaging both Facilities and key cross-functional clients and stakeholders
- Ensure appropriate internal and external resources are incorporated into the project design and execution
- Lead the scheduling, planning, control, and effective coordination of all parallel activities related to each project
- Maintain project schedule through minimal unanticipated schedule challenges
- Ensure that the construction project and the finished facility are compliant with all applicable safety, regulatory, legal requirements
- Achieve effective financial control through management of project scope, estimating, effective use of SAP, RPM, SRM, budget control tools, risk management, and project closeout
- Achieve high customer satisfaction by delivering finished projects on time that are fully commissioned, qualified, and ready for startup/occupancy, and meet all requirements of stakeholders
Required Qualifications
- Bachelor's degree in Engineering (Chemical/Mechanical preferred)
- -12 years' experience managing pharmaceutical capital projects, especially with API and/or Pilot Plant Facilities
- Experience managing multiple complex EPCMV projects ($10M - $50M+) using the Stage Gate Process
- Demonstrated success leading multi-disciplinary and multi-functional teams
- Demonstrated strength in stakeholder management
- Experience with Process Hazard Analysis (PHA), Process Safety Management (PSM), and Pre-Startup Safety Review (PSSR)
- Understanding of financial management as it relates to capital and expense spending and project cash flow forecasting
- Hands-on experience in the negotiation and management of contracts and agreements with engineering contractors, vendors, regulatory and government agencies
- Extensive knowledge of working with the unionized workforce
- Understanding of regulatory, environmental, GMP and OSHA regulations
- Understanding of functional requirements of pharmaceutical facilities, engineering best practices, design guidelines and standards, value engineering, closeout documentation standards, and life cycle costing
- Demonstrated Project Management expertise for design, construction, qualification, start-up, and tech transfer involving all areas of Pharmaceutical Manufacturing, Pilot Plants, and Research Facilities
- Experience interfacing with a variety of customers such as Manufacturing, Chemical Development, and Maintenance
Preferred Qualifications
- PMP certification
- EIT/PE License
Skills Required
- Interpersonal and collaboration skills necessary to interface with and influence all levels of management
- Excellent planning, organizing, analysis, and problem-solving skills
- Proficient in Microsoft Excel, Project, PowerPoint, SAP, RPM (Project Capital System), SRM (Purchase Order System)
Benefits & Perks
- Paid national holidays and optional holidays
- Global Shutdown Days between Christmas and New Year's holiday
- Up to 120 hours of paid vacation
- Up to two (2) paid days to volunteer
- Sick time off
- Summer hours flexibility
Locations
- Princeton NJ, United States
Salary
Estimated Salary Rangemedium confidence
150,000 - 250,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Interpersonal and collaboration skills necessary to interface with and influence all levels of managementintermediate
- Excellent planning, organizing, analysis, and problem-solving skillsintermediate
- Proficient in Microsoft Excel, Project, PowerPoint, SAP, RPM (Project Capital System), SRM (Purchase Order System)intermediate
Required Qualifications
- Bachelor's degree in Engineering (Chemical/Mechanical preferred) (experience)
- -12 years' experience managing pharmaceutical capital projects, especially with API and/or Pilot Plant Facilities (experience)
- Experience managing multiple complex EPCMV projects ($10M - $50M+) using the Stage Gate Process (experience)
- Demonstrated success leading multi-disciplinary and multi-functional teams (experience)
- Demonstrated strength in stakeholder management (experience)
- Experience with Process Hazard Analysis (PHA), Process Safety Management (PSM), and Pre-Startup Safety Review (PSSR) (experience)
- Understanding of financial management as it relates to capital and expense spending and project cash flow forecasting (experience)
- Hands-on experience in the negotiation and management of contracts and agreements with engineering contractors, vendors, regulatory and government agencies (experience)
- Extensive knowledge of working with the unionized workforce (experience)
- Understanding of regulatory, environmental, GMP and OSHA regulations (experience)
- Understanding of functional requirements of pharmaceutical facilities, engineering best practices, design guidelines and standards, value engineering, closeout documentation standards, and life cycle costing (experience)
- Demonstrated Project Management expertise for design, construction, qualification, start-up, and tech transfer involving all areas of Pharmaceutical Manufacturing, Pilot Plants, and Research Facilities (experience)
- Experience interfacing with a variety of customers such as Manufacturing, Chemical Development, and Maintenance (experience)
Preferred Qualifications
- PMP certification (experience)
- EIT/PE License (experience)
Responsibilities
- Lead the development of capital project scope, objectives, and delivery from concept to validation and startup process
- Drive effective project leadership, decision-making, and problem-solving through development of creative solutions
- Lead and promote effective teamwork by engaging both Facilities and key cross-functional clients and stakeholders
- Ensure appropriate internal and external resources are incorporated into the project design and execution
- Lead the scheduling, planning, control, and effective coordination of all parallel activities related to each project
- Maintain project schedule through minimal unanticipated schedule challenges
- Ensure that the construction project and the finished facility are compliant with all applicable safety, regulatory, legal requirements
- Achieve effective financial control through management of project scope, estimating, effective use of SAP, RPM, SRM, budget control tools, risk management, and project closeout
- Achieve high customer satisfaction by delivering finished projects on time that are fully commissioned, qualified, and ready for startup/occupancy, and meet all requirements of stakeholders
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
Tags & Categories
Senior Manager, Global Capital Project Delivery
Bristol-Myers Squibb
Senior Manager, Global Capital Project Delivery
Job Description
Lead the development of capital project scope, objectives, and delivery (from concept to validation and startup process) with emphasis on R&ED Laboratories and Chemical Development Projects in support of the business strategy concerning clients and stakeholders Drive effective project leadership, decision-making, and problem-solving through development of creative solutions as needed throughout lifecycle of projects Lead and promote effective teamwork by engaging both Facilities as well as key cross-functional clients and stakeholders to ensure appropriate internal and external resources are incorporated into the project design and execution Lead the scheduling, planning, control and effective coordination of all the parallel activities related to each project and maintain project schedule through minimal unanticipated schedule challenges Ensure that the construction project and the finished facility are compliant with all applicable safety, regulatory, legal requirements Achieve effective financial control through management of project scope, estimating, effective use of SAP, RPM, SRM, budget control tools, risk management, and project closeout Achieve high customer satisfaction by delivering finished projects on time that are fully commissioned, qualified and ready for startup/occupancy, and meet all requirements of stakeholders Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Bachelor's degree in Engineering (Chemical/Mechanical preferred). PMP certification & EIT/PE License a plus 8-12 years' experience managing pharmaceutical capital projects, especially with API and/or Pilot Plant Facilities Experience managing multiple complex EPCMV projects ($10M - $50M+) using the Stage Gate Process Demonstrated success leading multi-disciplinary and multi-functional teams and demonstrated strength in stakeholder management Experience with Process Hazard Analysis (PHA), Process Safety Management (PSM), and Pre-Startup Safety Review (PSSR) Understanding of financial management as it relates to capital and expense spending and project cash flow forecasting Hands-on experience in the negotiation and management of contracts and agreements with engineering contractors, vendors, regulatory and government agencies Extensive knowledge of working with the unionized workforce Understanding of regulatory, environmental, GMP and OSHA regulations, as well as functional requirements of pharmaceutical facilities, engineering best practices, design guidelines and standards, value engineering, closeout documentation standards, and life cycle costing Interpersonal and collaboration skills necessary to interface with and influence all levels of management Demonstrated Project Management expertise for design, construction, qualification, start-up, and tech transfer involving all areas of Pharmaceutical Manufacturing, Pilot Plants, and Research Facilities Experience interfacing with a variety of customers such as Manufacturing, Chemical Development, and Maintenance Excellent planning, organizing, analysis and problem-solving skills Proficient in Microsoft Excel, Project, PowerPoint, SAP, RPM (Project Capital System), SRM (Purchase Order System)
Key Responsibilities
- Lead the development of capital project scope, objectives, and delivery from concept to validation and startup process
- Drive effective project leadership, decision-making, and problem-solving through development of creative solutions
- Lead and promote effective teamwork by engaging both Facilities and key cross-functional clients and stakeholders
- Ensure appropriate internal and external resources are incorporated into the project design and execution
- Lead the scheduling, planning, control, and effective coordination of all parallel activities related to each project
- Maintain project schedule through minimal unanticipated schedule challenges
- Ensure that the construction project and the finished facility are compliant with all applicable safety, regulatory, legal requirements
- Achieve effective financial control through management of project scope, estimating, effective use of SAP, RPM, SRM, budget control tools, risk management, and project closeout
- Achieve high customer satisfaction by delivering finished projects on time that are fully commissioned, qualified, and ready for startup/occupancy, and meet all requirements of stakeholders
Required Qualifications
- Bachelor's degree in Engineering (Chemical/Mechanical preferred)
- -12 years' experience managing pharmaceutical capital projects, especially with API and/or Pilot Plant Facilities
- Experience managing multiple complex EPCMV projects ($10M - $50M+) using the Stage Gate Process
- Demonstrated success leading multi-disciplinary and multi-functional teams
- Demonstrated strength in stakeholder management
- Experience with Process Hazard Analysis (PHA), Process Safety Management (PSM), and Pre-Startup Safety Review (PSSR)
- Understanding of financial management as it relates to capital and expense spending and project cash flow forecasting
- Hands-on experience in the negotiation and management of contracts and agreements with engineering contractors, vendors, regulatory and government agencies
- Extensive knowledge of working with the unionized workforce
- Understanding of regulatory, environmental, GMP and OSHA regulations
- Understanding of functional requirements of pharmaceutical facilities, engineering best practices, design guidelines and standards, value engineering, closeout documentation standards, and life cycle costing
- Demonstrated Project Management expertise for design, construction, qualification, start-up, and tech transfer involving all areas of Pharmaceutical Manufacturing, Pilot Plants, and Research Facilities
- Experience interfacing with a variety of customers such as Manufacturing, Chemical Development, and Maintenance
Preferred Qualifications
- PMP certification
- EIT/PE License
Skills Required
- Interpersonal and collaboration skills necessary to interface with and influence all levels of management
- Excellent planning, organizing, analysis, and problem-solving skills
- Proficient in Microsoft Excel, Project, PowerPoint, SAP, RPM (Project Capital System), SRM (Purchase Order System)
Benefits & Perks
- Paid national holidays and optional holidays
- Global Shutdown Days between Christmas and New Year's holiday
- Up to 120 hours of paid vacation
- Up to two (2) paid days to volunteer
- Sick time off
- Summer hours flexibility
Locations
- Princeton NJ, United States
Salary
Estimated Salary Rangemedium confidence
150,000 - 250,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Interpersonal and collaboration skills necessary to interface with and influence all levels of managementintermediate
- Excellent planning, organizing, analysis, and problem-solving skillsintermediate
- Proficient in Microsoft Excel, Project, PowerPoint, SAP, RPM (Project Capital System), SRM (Purchase Order System)intermediate
Required Qualifications
- Bachelor's degree in Engineering (Chemical/Mechanical preferred) (experience)
- -12 years' experience managing pharmaceutical capital projects, especially with API and/or Pilot Plant Facilities (experience)
- Experience managing multiple complex EPCMV projects ($10M - $50M+) using the Stage Gate Process (experience)
- Demonstrated success leading multi-disciplinary and multi-functional teams (experience)
- Demonstrated strength in stakeholder management (experience)
- Experience with Process Hazard Analysis (PHA), Process Safety Management (PSM), and Pre-Startup Safety Review (PSSR) (experience)
- Understanding of financial management as it relates to capital and expense spending and project cash flow forecasting (experience)
- Hands-on experience in the negotiation and management of contracts and agreements with engineering contractors, vendors, regulatory and government agencies (experience)
- Extensive knowledge of working with the unionized workforce (experience)
- Understanding of regulatory, environmental, GMP and OSHA regulations (experience)
- Understanding of functional requirements of pharmaceutical facilities, engineering best practices, design guidelines and standards, value engineering, closeout documentation standards, and life cycle costing (experience)
- Demonstrated Project Management expertise for design, construction, qualification, start-up, and tech transfer involving all areas of Pharmaceutical Manufacturing, Pilot Plants, and Research Facilities (experience)
- Experience interfacing with a variety of customers such as Manufacturing, Chemical Development, and Maintenance (experience)
Preferred Qualifications
- PMP certification (experience)
- EIT/PE License (experience)
Responsibilities
- Lead the development of capital project scope, objectives, and delivery from concept to validation and startup process
- Drive effective project leadership, decision-making, and problem-solving through development of creative solutions
- Lead and promote effective teamwork by engaging both Facilities and key cross-functional clients and stakeholders
- Ensure appropriate internal and external resources are incorporated into the project design and execution
- Lead the scheduling, planning, control, and effective coordination of all parallel activities related to each project
- Maintain project schedule through minimal unanticipated schedule challenges
- Ensure that the construction project and the finished facility are compliant with all applicable safety, regulatory, legal requirements
- Achieve effective financial control through management of project scope, estimating, effective use of SAP, RPM, SRM, budget control tools, risk management, and project closeout
- Achieve high customer satisfaction by delivering finished projects on time that are fully commissioned, qualified, and ready for startup/occupancy, and meet all requirements of stakeholders
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
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