Director, Asset Management & Facilities, Biologics - Massachusetts, Ayer

The announced job offer is made public by the firm: Bristol Myers Squibb and it was included in jobs list the date of: 2022-10-22 in the website greenenergyjobsonline.com.

It is announced that they have a job offer at the category of Engineering and the jobs location is in the state of Massachusetts at the city Ayer, in the country US - at this current ZipCode: 01434

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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.

MAJOR DUTIES & RESPONSIBILITIES:

Biologics Global Manufacturing Operations Business Unit:

• Biologics Large Scale Cell Culture: Lead Asset Engineering (Maintenance & Metrology, P&S and MRO) and Building/Facilities maintenance operations in support of the Biologics Large Scale Cell Culture (LSCC) Commercial Manufacturing Operations. Biologics LSCC is a large commercial manufacturing operation producing Orencia and Empliciti within Biologics Global Manufacturing Operations business unit.
• Biologics Single Use Facility (SUF): Lead Asset Engineering (Maintenance & Metrology, P&S and MRO), and Building/Facilities maintenance operations in support of the Biologics Single Use Facility (SUF). Biologics SUF is a clinical and commercial small-scale manufacturing facility within Biologics Global Manufacturing Operations business unit.
• Biologics Network Cell Bank Operations: Lead Asset Engineering (Maintenance & Metrology, P&S and MRO), and Building/Facilities maintenance operations in support of the Biologics Cell Bank Operations. Biologics Cell Banking is a cell bank manufacturing and storage facility within Biologics Global Manufacturing Operations business unit.

Devens Site Support areas:

• Lead Asset Management (Maintenance & Metrology, P&S and MRO), operations in support of Warehouse and Laboratory Operations.
• Supports both Biologics and Cell Therapy manufacturing operations with Asset Information Management (CMMS - Maximo).
• Owns the asset management training program for both Biologics and Cell Therapy business units.
• Own the operation and maintenance of clean utilities (WFI and Clean Steam production)

Support business units, as follows:

• Is a senior member of the Site Engineering organization senior leadership team. As such, takes part in key decisions for the organization.
• Manages an overall budget of about $15MM, including service contracts in the range of $2-$4MM.
• Develop and implement state-of-the-art asset management (maintenance & metrology) systems to assure a high level of support for the Devens site.
• Support the development and implement processes that minimize inconsistencies or defects in equipment that could lead to variability in equipment/system output.
• In collaboration with the Systems Lifecycle Engineering organization, set and implement strategies to ensure that equipment is operating within specifications (i.e. process capability) that will produce high level of quality output, going beyond just preventing break downs, leveraging data and predictive analytics (including machine learning where applicable).
• In collaboration with the Site Facilities group, ensure that the manufacturing facility is always in inspection-ready state. In addition, establish relationship with our Integrated Facilities Management service provider to deliver facilities services within manufacturing building boundaries.
• Develop and implement strategies to keep our employees safe and to develop them into a high performing organization.
• Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while maintaining highly compliant facilities.
• Provide Leadership and overall management of the maintenance operations at the Devens site including all on-site and subcontracted trades to maintain a fully functional GMP process development and manufacturing facility.
• Maintenance Operations include the daily activities as well as regularly scheduled activities such as preventative maintenance and area shutdown activities to limit manufacturing disruption, maintenance planning & scheduling, reliability centered maintenance (RCM), MRO and all mechanical, electrical and instrumentation services.
• Ability to communicate a clear vision aligned with Site and Overall Business objectives.
• Broad knowledge of Good Manufacturing Practices, Governing Building Codes, OSHA regulations, and Industry Regulations related to the manufacture of Pharmaceutical products.
• Develop and implement performance targets for Maintenance that creates a commitment to superior quality and safety from the staff.
• Develops relationships with diverse groups across the client base at the Devens site. Work within a team environment with other Site Engineering functions, including Engineering and Plant Engineering in a matrix organization.
• As a member of the Site Engineering Maintenance team, will initiate projects together with other functional groups and review engineering drawings, specifications, and major maintenance operations.
• Customer Service is paramount, therefore must build and sustain strong relationships with internal and external stakeholders including Manufacturing, Quality, EHS, and local community and regulatory agencies to meet site and Business requirements.
• Periodically will assess with the customer that expected service level is being attained and must strive to exceed such expectations. Will interface with regulatory bodies and be accountable for non-conformance investigation thoroughness with appropriate and timely CAPA implementation. Ensure compliance with plant safety regulations and environmental regulatory requirements.

KNOWLEDGE AND SKILLS:

• Knowledge of maintenance, utility operations and engineering generally attained through studies resulting in a Bachelor of Science degree in Mechanical Engineering, Electrical, Chemical Engineering, related discipline, or its equivalent is required
• Minimum 12 years pharmaceutical industry experience related to Engineering and or Maintenance activities and operations.
• Mastery of an engineering field and pharmaceutical processes such as building systems, manufacturing operations, etc.
• Understanding of building maintenance activities and functions.
• Specific knowledge of equipment reliability principles and processes as related to maintenance practices.
• Exposure to upstream cell culture and downstream purification processes a plus.
• Knowledge of clean utilities water for injection, pure steam and clean room technology and maintenance of a cGMP facility.
• Working knowledge of FDA regulations, fundamental principles, and operating implementation for electrical, HVAC, process heating and cooling utilities.
• Ability to manage or be an active team member of cross-functional project teams.
• Must have a BA degree in engineering or equivalent experience.
• Knowledge of BMS business objectives, strategies, and the pharmaceutical industry. Understanding of regulatory, environmental, GMP GLP and OSHA regulations.

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 . Visit to access our complete Equal Employment Opportunity statement.
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