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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 .

To supervise the daily job assignments in support of building utilities ensuring compliance with company policy and appropriate regulatory standards on day shift.

Key Responsibilities :

• Role will support of the following operations at the BMS Devens campus: Biologics Large Scale Commercial Manufacturing, Biologics Clinical Manufacturing, Biologics Cell Bank Manufacturing, Biologics Development and Laboratory operations, and CAR-T (Cell Therapy) Manufacturing

• Assures completion of all production maintenance activities (e.g., pm's, pdm's, work orders, safety inspection, area projects, day-to-day equipment and systems support) for the site by coordinating maintenance services with other operations leaders and planning personnel.

• Develops new systems, practices and procedures to enhance the performance of the business.

• Troubleshoots routine and unusual technical / administrative problems. Manages the use and application of all Maintenance Tools.

• Develops and/or approves SOPs and other technical documentation required for Operations and Maintenance.

• Works with the Spare Parts group to ensure proper materials and parts are identified and available to sustain Corrective activities.

• Provides support to other departments in the investigations and resolutions of Maintenance related Quality Events.

• Support basic risk mitigations options and advanced troubleshooting to identify root cause and appropriate corrective actions for equipment system problems.

• Provides a clear vision, defining specific and timely objectives and monitoring team activities, providing specific feedback to motivate, build competencies and enhance performance.

• Maintains a thorough knowledge of short and long range business priorities and objectives through regular communication with site management adjusting Maintenance execution to ensure alignment with strategy and goals.

• Ensures field personnel are current in their training; maintains current status of the training curricula of direct reports.

• Develop personnel and manages performance. Develops and implements Key Performance Indicators (KPIs) and establish goals to accomplish World-Class Maintenance performance.

• Active member of all Reliability Centered Maintenance (RCM) initiatives by participating in and/or providing resources to improve the reliability of our systems, equipment and operations.

• Identifies areas of opportunities to optimize equipment and systems using Maintenance Programs data, evaluating the impact on policies and regulations, allocating Capital or expenses required, developing action plans and implementing.

• Ensures Job Plans are current and in order to apply the proper Preventive, Predictive Maintenance procedures.

• Establishes specific expectations and objectives to ensure compliance with EHS guidelines, cGMP regulations, Company policies and other external agency regulations.

• Supports the development of related procedures and programs, implement and monitor performance.

• Identifies areas of opportunity and prepare specific action plans to increase awareness and to maintain compliance.

• Processes QE's, CAPA's and Audit responses according to established due dates.

• Troubleshoot customer service calls.

• Individual will partner with subject matter experts (SME) & Reliability services to trouble operational issues.

• Ensures that all appropriate R&M data (e.g., material costs, contract labor costs, effort) is captured on a work order.

• Responsible for the effective uninterrupted support of Facilities operational activities for BMS Devens.

• Cross train and / or back up, as appropriate to the advanced level. Maintain up to date and complete system documentation in a central resource location for all repairs or changes to the system.

• Analyze the operation of various systems, determine the cause of any problems/malfunctions and take corrective action as required.

• Comply with departmental policy for the safe storage, usage, and disposal of hazardous materials. Maintain a clean and safe workplace. Conduct immediate clean-up of work area, returning tools to workshop, and unused supplies to store room.

• Report any equipment problems, impending supply or material shortages to the Operations Manager.

• Maintains tools and orders supplies as required for installation and repairs.

• Complies with departmental policy for the safe storage, usage and disposal of hazardous materials.

Education & Experience :

• Knowledge of Maintenance, Operations and Engineering generally attained through studies resulting in a B.S., in engineering, or related discipline.

• A minimum of 5 years of experience in Maintenance, Operations of Clean Utilities and/or Biologic Process Manufacturing and Manufacturing equipment support.

• Ability to provide support during external and internal regulatory audits (FDA, EMEA, etc.).

• Previous lead experience which demonstrates proficiency in selection, motivating and retaining a superior team, effectively managing personnel issues and planning and administering financial resources.

• Knowledge of Maximo or other CMMS applications required.

• Managing personnel issues and planning and administering financial resources.

• Demonstrated aptitude for engineering principles and building and/or manufacturing automation systems.

• Knowledge of Maximo or other CMMS applications required.

• Experience in working in an environment governed by SOPs and cGMPs and the know-how to work and manage within a regulatory oversight.

• Adaptable to a fast paced, complex and ever changing business environment.

• Strong analytical and communication skills are critical.

#LI-Onsite #BMSBLDMA #DVNENGINEER

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: R1584887

Updated: 2024-09-15 02:43:01.796 UTC

Location: Devens-MA

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.