Associate Director, Maintenance and Reliability

Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
One shared journey is moving us forward at Bristol-Myers Squibb.
Around the world, we are passionate about making an impact on the lives of patients with serious disease.
Empowered to apply our individual talents and ideas so that we can learn and grow together.
And driven to make a difference, from innovative research to hands-on community support.
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 has announced plans for an expansion of its large-scale biologics manufacturing facility in Devens, Massachusetts.
The expansion will create a mammalian cell biologics center of excellence through the introduction of biologics development and clinical trial manufacturing capabilities to the site.
Both represent new capabilities for Devens, a site that in its early years has focused solely on large-scale, bulk biologics manufacturing.
The Associate Director, Maintenance and Reliability develops and implements state-of-the-art reliability and maintenance systems to assure a high level of support for the Devens site.
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.
Responsibilities include but are not limited to:
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.
Maintenance operations include the daily activities as well as regularly scheduled activities such as preventative maintenance and shutdown activities to limit manufacturing disruption, maintenance planning & scheduling, reliability centered maintenance (RCM), MRO and all mechanical, electrical and instrumentation services.
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 Technical Services functions, including Engineering and Plant Engineering in a matrix organization.
As a member of the Technical Services 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.
Qualifications BS in Engineering or equivalent experience 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 within BioPharma industry is preferred.
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.
Bristol-Myers Squibb is an equal opportunity employer - Vet/Disability - 1501337

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