Bristol Myers Squibb Director of Global Capital Project Engineering in Cambridge, Massachusetts
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
Principle Objective of Position
The Director, Global Capital Project Engineering supports Global Engineering & Facilities (GEF) capital construction projects across either a dedicated site or multiple sites within Global Product Development & Supply (GPS) and Research & Early Development (R & ED). This leader will directly manage a portfolio of site-specific capital projects and lifecycle execution of these capital projects with project controls methodologies in accordance with the Global Engineering Governance model and standards. This role will directly manage and provide guidance to both full time employees and contracted resources at their site and apply their knowledge (industry information, internal best practices and standards) to deliver the portfolio of capital projects on schedule and within budget. The capital project portfolio per site ranges from a few million dollars to an overall aggregate budget of several hundred million. This position will be directly responsible for a large ($300M - $400M) state of the art life science capital project.
Major Duties and Responsibilities
Strong significant pharmaceutical construction project management skills and proven experience in managing a portfolio of capital projects with emphasis on R&ED Laboratories and Chemical Development Projects, as well as site utility and infrastructure upgrades.
Ensure compliance with Bristol-Myers Squibb Global Engineering Governance model, standards and finance requirements.
Provide experienced project controls oversight of capital projects through regular review of change requests, schedule, accurate cost and cash flow projections, risk management, project monthly reporting and financial audit preparation.
Routinely work with Global Engineering, Finance and sites to develop and analyze capital project cash flow forecasts and suggest risk adjustments, as required.
Mentor, drive and lead network learning, and best practice sharing to build an efficient and productive department.
Provide leadership in the management of relationships between Global Engineering, Facilities, Procurement and all additional enabling functions to deliver all capital projects to all our end users.
Experience with Process Hazard Analysis (PHA), Process Safety Management (PSM), and Pre-Startup Safety Review (PSSR). Background in the use of the Stage Gate Process. Understanding of financial management as it relates to capital and expense spending and project cash flow forecasting. Understanding of regulatory, environmental, GMP and OSHA regulations.
Familiar with the use of RPM (Project Capital System) and SRM (Purchase Order System). Pro-active in solving challenging project issues with the ability to develop creative solutions.
Experience in total project delivery (from concept to validation / commissioning and startup process). Leads the development of the capital project scope and objectives in support of the business strategy concerning clients and stakeholders.
Exhibits strong project leadership and effective decision making throughout each project. Manages and promotes effective teamwork by engaging both Facilities as well as including key clients and stakeholders.
Leads the scheduling, planning, control and effective coordination of all the parallel activities related to each project and maintains project schedule through minimal unanticipated schedule challenges.
Possesses broad knowledge of the functional requirements of pharmaceutical facilities and engineering best practices, while ensuring that appropriate internal and external resources are incorporated into the project design and execution.
Achieves a cost-effective, functional outcome with the use of design guidelines and standards, value engineering, life cycle costing and engineering best practices.
Assures that the construction project and the finished facility are compliant with all applicable safety, regulatory, legal requirements.
Achieves effective financial control through management of project scope, estimating, effective use of SAP, RPM, SRM, budget control tools, risk management, and project closeout.
Achieves high customer satisfaction by delivering finished projects that are fully commissioned, qualified and ready for startup/occupancy and meets all requirements of stakeholders and stays within a predetermined schedule.
Strong understanding of construction terminology and legal content of construction contracts and documents.
Extremely proficient with closeout documentation standards.
Bachelor’s degree in Engineering (preferred in Chemical or Mechanical). EIT/PE License a plus.
Minimum 10-15 years’ experience managing pharmaceutical projects, especially with API and/or Pilot Plant Facilities.
Experience managing both individuals as well as teams overseeing multiple complex EPCMV projects ($100,000,000 - $400,000,000).
Demonstrated success leading multi-disciplinary and multi-functional teams and demonstrated strength in stakeholder management.
Excellent planning, organizing, analysis and problem-solving skills
Strong seasoned background and understanding in the planning, design, procurement, scheduling, execution and closure of projects
Demonstrated project controls skills in budgeting, project change management, reporting and forecasting, scheduling, claims and management
Demonstrated business acumen
Ability to participate in change event analysis and estimating
Ability to use discretion with sensitive/confidential information
Proficient in Microsoft Excel, Project, PowerPoint and SAP
Excellent interpersonal, verbal, written and presentation communication skill
Extensive knowledge of working with the unionized workforce.
Interpersonal / facilitation skills necessary to interface with and influence all levels of management.
Experiences in technical transfer of technology and concepts.
Demonstrated Project Management expertise for design, construction, qualification and start-up involving all areas of Pharmaceutical Manufacturing, Pilot Plants, and Research Facilities.
Hands on experience in the negotiation and management of contracts and agreements with engineering contractors, vendors, regulatory and government agencies.
Previous seasoned interactions with a variety of customers, such as manufacturing, Chem Development, and maintenance.
Physical / Mental Demands
Occasional stooping, bending, stretching, pushing, pulling, reaching and/or light lifting may be required
Ability to sit, stand, walk and move within workspace for extended periods
Ability to perform repetitive tasks including hand to finger manipulations, grasping, pushing and pulling.
Ability to climb ladders and work in elevated areas.
Minimal travel in North America and possibly abroad
Environment may include working in office or in a laboratory / manufacturing area.
Ability to work safely in an environment with hazardous, radioactive, and infectious materials and waste.
Ability to work safely in an environment with exposure to high temperature / pressure steam, and other fluids, compressed gasses, odors, various noise levels, moving parts, vibration, wet / slippery areas and high voltage energy supplies
Environment may include working at heights, in cold temperatures, and/or constricted spaces
Ability to work safely when working alone or working with others.
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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.
Company: Bristol Myers Squibb
Req Number: R1529081-en-us
Updated: 2020-10-25 23:09:37.556 UTC
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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