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Innova Solutions is immediately hiring for a Facility & Reliability Engineer Position type: Full-time Contract Duration: 12 Months Location: Summit, NJ 07901 (Onsite) As a Facility & Reliability Engineer, you will: The purpose of the Facility and Reliability Engineer is to development and implement a Reliability Centered Maintenance (RCM) strategy to support Summit West Cell Therapy Operations and to maintain a qualified and compliant facility operation status. Their main responsibility will be the execution of the reliability program. The Facility & Reliability Engineer will also support the successful operation of facility, laboratory, and business functions at multi-use GMP West Cell Therapy Operations, through interaction with internal customers and external service providers. The role is expected to be able to identify issues or unmet needs and initiate projects or programs to address them. This individual works collaboratively to complete assignments and oversees the successful completion of tasks. Using solid analytical skills, the incumbent can recognize problems of moderate scope and complexity and independently develop potential solutions and courses of action. This individual represents the work group on multi-disciplinary and cross-functional teams and uses established relationships to influence and lead teams and stakeholders with fact-based, business value knowledge. Knowledge, Skills, And Abilities: * Strong understanding of building systems including life-safety, lighting, mechanical, electrical, plumbing, and HVAC * Strong knowledge of critical utility systems such as compressed gas, vacuum, waste * Strong knowledge of and understanding of Computerized Maintenance Management Systems (CMMS) * Maintains a high level of multi-tasking ability in conjunction with proven organizational skills Ability to prioritize assigned tasks in a high paced GMP environment and concurrently monitor tasks with others that may impact timely completion * Knowledge of FDA / EU / PDMA / IGJ, GxP environments, ISO, and associated compliance regulations * Adept in Microsoft Office Suite - Word, PowerPoint, MS Project, Excel, Outlook, and Visio with the ability to learn new software, such as enterprise business, building management, and security * Proficient at writing well-formulated emails and notifications. Ability to effectively communicate with employees, contractors, and vendors. Ability to follow oral and written instructions, read, interpret and update engineering manuals/drawings relevant to the trade or the assigned task. * Self-starter who can work independently without direct supervision and in a cross-functional team environment * Knowledge of IBC/IFC building codes, OSHA, NFP, FM, LPDS and UL Core Competencies: * Technical knowledge of Reliability Engineering * Technical Writing * Problem Solving / Troubleshooting * Team Player * Customer Focused * Action Oriented Preferred: Bachelor's degree in mechanical or industrial engineering 3+ years of reliability engineering 3+ years working in GxP environments. Lean six sigma knowledge. Required: 3+ years working in engineering or facilities. 3+ years working in manufacturing environments. Duties And Responsibilities: Facility Asset Management * Provides technical expertise, troubleshooting and improved equipment maintenance/reliability strategies to optimize safe, compliant, and efficient operations of all facility and utility equipment and instrumentation. * Prepares asset files including equipment data sheets, impact assessments, P&ID & drawings, factory O&Ms, factory maintenance recommendations, maintenance work plans and procedures. * Assist in the development and management of a facility document management program to track facility drawings, and project turnover packages * Lead on facility workstream to support large-scale project asset and maintenance plan management. Project will require the ability to identify and manage contract support to execute according to project schedule. * Manage logbook strategies for facility equipment owned and maintained by GMP Facilities. * Preventative Maintenance Work Plans * Establishes effective preventative and predictive maintenance plans for GMP Pharmaceutical facility & process utility equipment according to OEM recommendations, industry standards and process application * Generates SOPs and Work Practices within Celgene's Document Management System and electronic work plan template and measurement data templates to establish the Use, Maintenance and Calibration plans for GMP equipment * Works with vendors to define vendor requirements to support maintenance or calibration plans and contracts * Initiates deviations for maintenance work orders that are out of coTo view the full job description, click here