Facilities Engineer

Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Job Description Summary

The Facilities Management team is responsible for the compliant maintenance and operation of GMP programs in support of manufacturing life-saving medicines (such as the pest control program, the GMP cleaning program, and overall facilities management). This group ensures adherence to SOPs and cGMPs and executes projects to improve the safety, efficiency, reliability, and compliance of these programs. They oversee maintenance and contractor activities, coordinate activities in support of system shutdowns, and lead investigations related to these systems. Members of this team serve as subject matter experts (SMEs) for these programs on project teams, and during regulatory inspections. The members of this team are expected to focus on the GMP systems to ensure compliance and to ensure the overall condition of the facility is maintained in a manner appropriate for GMP manufacturing.

Facilities Engineer (GMP Services)

RESPONSIBILITIES


Responsible for maintaining the facility and GMP facility programs in compliance with local, county, state, and federal regulations.

Identifies and manages projects that meet operational goals in terms of safety, quality, output and cost.

Identifies and resolves issues with preventive maintenance and the repairs of the building envelope, pest control, GMP facility cleaning, electrical, mechanical, HVAC, security systems as well as other related building systems working with third party vendors.

Effectively communicates with clients to support regulatory agencies (FDA, EMEA etc.) and internal project teams for inspection readiness.

Build and sustain strong customer service relationships with internal and external stakeholders to meet site and business requirements.

Ensure compliance of pest control program and GMP cleaning program with GMPs, industry best practices, and BMS directives.

Develop the pest control program into a best-in-class program through continuous innovation, performing data and trend analysis, identifying proactive improvements, performing root cause analysis, and implementing meaningful CAPA.

Serve as a site SME for the site pest control program and the GMP cleaning program and interact with regulatory authorities or internal auditors. Ensure inspection-readiness of key systems. Develop responses and action plans to correct any deficiencies.

Identify continuous improvement, energy conservation, and cost savings opportunities.

Maintain and revise standard operating procedures (SOPs) governing pest control, GMP facility cleaning, and other pertinent systems. Train in-house technicians and contractors as required.


QUALIFICATIONS


Bachelor of Science in Engineering or other related discipline.

Knowledge of pharmaceutical classified environments, building construction, pest control and facility cleaning in a GMP environment, and building systems.

Demonstrated ability to work across organizational boundaries to resolve a range of technical and compliance issues.

Technical knowledge in a focus area such as pest control, facility cleaning, and facilities engineering is desired.

Facility-related (e.g. mechanical, electrical) assessment and troubleshooting skills.

Project management skills (i.e. budget tracking, schedule development and adherence, project reporting, etc.)

Strong analytical and problem solving skills.

Willingness to provide on-call, off-hours support as needed to assist with planned activities or respond to unplanned problems.

Understanding of applicable regulations (GMP, OSHA, DEC, etc.).

Familiarity with quality systems governing GMP facilities (change control, SOPs, investigations, CAPAs).

Technical writing skills and effective presentation skills are required.


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 the resources to pursue their goals, both at work and in their personal lives.

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, disability or protected veteran status.

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