Job Description

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.

Purpose and Scope of Position

The Principal Plant Engineer is responsible for the management of multi-discipline projects, the creation/revision of engineering documentation, as well as management of external engineers and/or architects as required by each assignment.  Projects range from small scale facility modifications/independent equipment to large scale, multi-discipline, complex equipment/system installations and/or major facility modifications, as well as site improvements. Also performing investigations and developing reports/responses.

The Principal Plant Engineer is responsible for running cross-functional internal project teams of customer processes from initiation through project closeout and will be the primary internal and external contact regarding the day-to-day execution of the project.

Required Competencies:  Knowledge, Skills, and Abilities

• Advanced knowledge of mechanical, utility and plant systems, as well as the ability to read construction and process drawings.
• Advanced knowledge of quality control systems, cGMP engineering design practices, facility and construction processes/equipment, manufacturing equipment project management, OSHA regulations as well as any other regulatory agencies the facility adheres to.
• Intermediate knowledge of Lean Manufacturing principles.
• Flexibility and ability to multi-task.
• Advanced organizational and time management skills.
• Advanced teamwork and facilitation skills.
• Ability to solve complex problems.
• Advanced critical reasoning and decision-making skills.
• Advanced written and verbal communication skills and the ability to interpret / write general business documents.
• Advanced knowledge of MS Word, Outlook, Excel, MS Project, PowerPoint, and AutoCAD.
• Basic knowledge of the Pharmaceutical Industry as related to cGMP, regulatory standards, quality systems and Biotech processes.

Duties and Responsibilities

• Primarily responsible for manufacturing utility systems including WFI, Pure Air, Pure Steam, Natural Gas, Nitrogen, HVAC, and others.
• Manage engineering projects to improve plant utility systems. Seek out and apply novel engineering approaches.
• Coordinate projects and maintenance activities with operations in order to minimize disruption.
• Provide technical guidance for maintenance technicians, outside service providers, and operations users.
• Engage with Facilities, Maintenance, Global Engineering, and external resources to engineer solutions.
• Review and approve drawings and other technical documentation to ensure that it remains current.
• Ensure compliance of GMP critical utilities with GMPs, industry best practices, and BMS directives.
• Investigate adverse trends and implement corrective actions.
• Create or contribute to quality plans that ensure orderly service interruptions and smooth return to service.
• Collaborate with other functions, such as quality assurance or EHS, to resolve compliance issues.
• Remain informed about the current industry practices and guidelines for critical utilities.
• Respond to unplanned outages in order to minimize disruption to manufacturing operations.
• Issue or contribute to safety permits and job hazard analyses (JHAs) to ensure the safe execution of projects or maintenance activities.
• Serve as a site SME for critical utility systems and interact with regulatory authorities or internal auditors. Ensure inspection-readiness of key systems. Develop responses or action plans to correct any deficiencies.
• Leverage appropriate resources from our site facilities and maintenance departments
• Identify continuous improvement, energy conservation, and cost savings opportunities.
• Apply modern reliability concepts to ensure effective maintenance and prevent failures.
• Maintain and revise standard operating procedures (SOPs) governing system operation and maintenance. Train in-house technicians and contractors as required.
• Perform other tasks as assigned.

Education and Experience

• Bachelor’s degree preferred, preferably in Engineering or related science.
• Advanced degree preferred.
• 7 years’ relevant work experience required, preferably in a pharmaceutical or engineering environment.
• Project management experience preferred.
• Aseptic Manufacturing experience preferred.
• An equivalent combination of education, experience and training may substitute.

Working Conditions

• The incumbent may be required to climb ladders or walk on catwalks at elevations above the floor to include walking on the roof.
• The incumbent may be exposed to areas where noise levels are elevated.  May require hearing protection during these times.
• The incumbent may be required to walk outside for short periods of time.
• The incumbent may be exposed to conditions that require safety glasses and hairnets.
• The incumbent may be exposed to noise, gases, odors, and wet/slippery conditions.
• The incumbent may be required to travel <10% (Domestic and International).
• Must be able to work at least 8 hours per day or longer during shutdown periods.
• Requires the ability to concentrate during lengthy technical discussions.

VETERAN

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. 

Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.

To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation.  Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment.  This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.