Manager, Compliance Facility Utility and General Maintenance

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. 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 . Schedule- 8am-430pm. MAJOR DUTIES AND RESPONSIBILITIES:    1. Initiates, documents, and supports deviation records and supplemental reports to investigate atypical events within the Engineering organization, including leading investigations and deviation supplementals as required. 2. Acknowledge and conducts investigations and deviations supplementals for facilities, utilities and/or maintenance deviations and supplementals. Accountable for Corrective Actions and Preventive Actions (CAPA) or actions related to regulatory observations, internal audits or deviations within the engineering department. 3. Supports readiness of the facility for regulatory inspection. Represents the maintenance department during regulatory agency inspections such as FDA / EMEA and/or during internal company audits. 4. Support maintenance and calibrations quality agreements discussion and approvals. 5. Collaborates with cross‑functional partners, including Quality, EHS, Manufacturing Technology, Production, and Planning and Scheduling, to ensure alignment of objectives and compliance with site and organizational goals. 6. Develops, reviews, approves, and implements departmental procedures and forms to ensure alignment with current practices, evolving GMP expectations, and established periodic review requirements. 7. Ensures site compliance with corporate systems through the evaluation, implementation, and enforcement of company policies, standards, and guidelines. 8. Supports the site Quality Risk Management program through participation in multidisciplinary teams and risk‑based decision‑making activities. 9. Develops and documents impact assessments related to the implementation of corporate policies and directives, and ensures timely execution in accordance with established implementation schedules. 10. Supports the site Inspection Readiness Program to ensure continuous preparedness for regulatory and internal audits. 11. Provides compliance support to site‑level projects, ensuring alignment with applicable quality systems, regulatory requirements, and engineering standards. 12. Provides compliance oversight and verifying compliance with BMS and WWQ&C Policies and Guidelines and site cGMP compliance policies and procedures are addressed. 13. Supports regulatory inspections and compliance initiatives, including preparation, execution support, and follow‑up activities. 14. Supports the Engineering Department Records Retention Program in accordance with corporate policies and regulatory requirements. 15. Initiates, evaluates, reviews, approves, and follows up on change controls for the Manatí site, including coordination and alignment with corporate support functions. 16. Applies and reinforces critical and analytical thinking throughout the change control and deviation management processes to ensure compliant, risk‑based decisions. 17. Participates in tiered governance meetings, departmental staff meetings, planning forums, and change control board meetings as required. 18. Maintains effective communication with internal and external