**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 rich in diversity. 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 . **Position:** Maintenance Specialist **Location** : Manatí PR **Key Responsibilities** 1. Ensure Asset Criticality ranking is performed to all area assets and define its maintenance strategy based in the asset criticality. 2. Ensures all critical systems/assets meet customer needs. Implement or propose alterations, modifications, or replacement of existing equipment to reduce maintenance costs, equipment downtime or improve reliability. 3. Responsible and accountable for job plans used for execution of Maintenance in a Biopharmaceutical manufacturing plant. This includes review andapproval of all changes to job plans as a result of Feedback to Planner, change control, equipment modification, etc, and ensuring material and task lists are accurate for right first-time execution of maintenance activities. 4. Provide support to all maintenance technicians to assist with troubleshooting, act as Subject matter expert for technical questions, and ensure job plans are accurate and able to be safely executed. Ensure vendor completed work meets the necessary maintenance standards and is handed over appropriately. Prepare troubleshooting guides as required by the asset and/or system. 5. Ensure equipment is accessible to all maintenance technicians to ensure safe execution of work. Work with maintenance and EHS teams to develop/revise Job Hazard Analysis (JHA) for PMs and troubleshooting guides. Update both as needed as a result of changes or continuous improvement. 6. Ensures sustainable business process for changes related to job plans, LOTO, and JHA as needed. 7. Own and drive/support operational excellence regarding Maintenance execution, including cost benefit analysis, review and/or creation of metrics and KPI related to maintenance execution. This may also include working with project engineering to support development of small capital projects to support changes to equipment configuration to support configuration. 8. Develops new systems, practices, policies, and procedures pertaining to maintenance and operations activities to enhance the performance of the business. 9. Ensures the application of mechanical and electrical technology, best practices, business trends and how to gain access and implement to maintain level of continuous improvement. 10. Prepares and manages maintenance capital projects for new equipment installations and major equipment overhauls including project scope development, design, procurement, project management up to commissioning and qualification activities. 11. Seeks clear communication with clients to develop the scope, cost and schedule for capital projects as well as develops justification and completes documents required to obtain project approval and to understand specific customer and stakeholder requirements and works across organizational and functional boundaries to assure that customers, peers, and support groups have an understanding of the scope and deliverables for all projects. 12. Fosters the understanding of the client/customer needs and integrates the operational support in meeting their requirements. 13. Provides user training and continuous support to assure proper use of the equipment following established operational procedures and manufacturing specifications and sound problem solving techniques to resolve issues and qualification problems. 14. Generates, evaluates, and closes change control documentation assuring the validation and compliance state of the equipment. 15. Provides project status using project plans and perform best efforts to achieve projects milestones within the pre-established due dates. 16. Provides alternatives and problem-solving initiatives during possible project delays or possible showstoppers. 17. Prepares procedures and defines standards for equipment performance optimization. 18. Contact equipment vendors (if applicable) to report problems. Coordinate and implement vendor recommendations when approved or accepted by the area Supervisors or Manager. 19. Understands spare parts needed for routine maintenance and ensures spare parts are available for run to failure equipment. Manage along with STORES the process for replacement of the obsolete parts and storage conditions. 20. For new equipment introduction, works with System Owner, Functional User, project engineering and design engineer or vendor, as needed, to develop necessary training for maintenance technicians, and to develop new maintenance strategy and job plans. This includes that appropriate materials, parts, tools, and skill sets are available to accomplish the work safely. May require travel to attend factory acceptance testing (FAT). 21. Works with management on development of sustainable business process for new equipment introduction. 22. Support training of maintenance staff on Techniques, new practices, and technologies. This may include review and approval of documents such as work instructions, procedures, and training guidelines used to support work execution and technician training. 23. Works closely with Reliability team to embed Reliability Centered Maintenance (RCM) initiatives to improve the reliability of our systems, equipment, and operations Identify areas of opportunities to optimize equipment and systems using Maintenance Program historical data. Assist with implementation of Predictive Maintenance, and introduction of new technology to support the program and participate in review of failure tracking and trending for executed work. 24. Ensure program meets necessary compliance requirements. This may include providing evaluation of the Maintenance Program against impacting policies and regulations, support of compliance investigations, CAPA, and change control impact assessments and support of health authority or internal audits. 25. Ensure compliance with EHS guidelines, cGMP regulations, Company policies and other external agency regulations. 26. Support the development of related procedures and programs related to Condition Based Monitoring or maintenance best practices such as Lubrication, precision maintenance and operator driven reliability. 27. Works closely with management on the development of departmental budget. 28. Works closely with Planning and Scheduling to develop standards for major maintenance overhauls and outages, specifically for Shutdown periods. 29. Participate in and lead Root Cause Analysis, Failure Mode, and Effects Analysis (FMEA) exercises in conjunction with Reliability Engineer, System Owners, Maintenance Technicians and Manufacturing Operators. **Qualifications & Experience** • BS in Engineering (Electrical, Computer, Mechanical, or related fields). • Six (6) years of experience in manufacturing operations in parenteral pharmaceutical environment. Knowledge of maintenance, operations and engineering generally attained through studies resulting in a B.S., in engineering, related discipline, or its equivalent experience. • A minimum of 6 years of experience in maintenance, engineering or operations of biologic process manufacturing and manufacturing equipment support or equivalent. • Knowledge of Maximo or other CMMS applications required. • Demonstrated aptitude for engineering principles and building and/or manufacturing automation systems. • Experience in working in an environment governed by SOPs and cGMPs and the know-how to work and manage within a regulated environment. • Adaptable to a fast paced, complex, and ever-changing business environment. • Ability to collaborate and work in a team environment; lead small projects and development of maintenance strategies. • Strong analytical and communication skills are critical. • Willing to provide on call support to a 24/7 manufacturing site, and work nights or weekends when needed to support emergent issue resolution or project implementation. • Experience in maintenance and or Technical Services, bio pharmaceutical equipment is preferred • In-depth knowledge of the science and physics involved in the implementation of computerized systems and automation as applied to pharmaceutical production environment. • Ability to provide support during external and internal regulatory audits (FDA, EMEA, Otsuka, Sanofi, etc.) • Excellent knowledge of electrical controls theory and electronic circuitry. • Ability to communicate, collaborate and interact effectively with people with a variety of levels and disciplines including internal and external customers, vendors, contractors, and operations staff. • Ability to exercise good judgment • Able to read, interprets, and understands electrical/mechanical drawings. • Ability to analyze equipment design opportunities and to identify and develop technical solutions. • Technical writing skills. • Ability to plan and prioritize multiple complex activities simultaneously by using sound Project Management Skills. • Ability to review SOPs and work instructions. • Flexible and responsible. • Significant ability and aptitude analyzing data to detecting inconsistencies, determining relative importance and to solve complex technical situations based on data. • Bilingual English/Spanish, both written and verbal are required • Willing to work irregular hours, shifts, weekends, and holidays. 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. **\#LI-Onsite** **BMSBL** 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. **Uniquely Interesting Work, Life-changing Careers** With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. **On-site Protocol** BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. 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/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. **Company:** Bristol-Myers Squibb **Req Number:** R1586907 **Updated:** 2024-11-10 02:20:21.003 UTC **Location:** Manati-PR 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.