Pfizer
Manager, Reliability Engineering
The Manager, Reliability Engineering functions as part of an integrated team to provide Maintenance and Engineering support to on-going sterile injectable operation areas of the Rochester, MI plant. This position works directly with the area Maintenance Team Leader and is integrated with the team of craftsmen and enablers who support that same operating area of responsibility. General responsibilities are to provide the technical program leadership and implementation activities to maximize the maintenance-related uptime and operating efficiencies of equipment and facility assets. The Manager, Reliability Engineering is also responsible for optimizing Preventative Maintenance (PM) strategies and updating the associated planning and tracking systems. This position interacts extensively with the Operations Area in a business partner arrangement to achieve mutual production and uptime goals. The Manager, Reliability Engineering also functions as an integral team member and Subject Matter Expert to support Master Planning & Capital Project upgrades in the area of responsibility. The Rochester site is a penicillin manufacturing facility. Candidates must not be allergic to penicillin. What You Will Achieve In this role, you will: Work closely with Production and Project Engineering to target maintainability issues, lower maintenance costs, and implement improvements. Establish the initial preventive maintenance and calibration activities for equipment / instruments that are in accordance with the guidelines and specifications for that particular equipment / instrument class. Extend, deactivate, and/or update PM and Calibration activities through utilization of the PM / Calibration Optimization and Rationalization Program processes. Select the initial Maintenance Strategy for new equipment and provides updates to keep the strategy current. Implement equipment reliability plans by ensuring job plans and tasks are established for Preventative Maintenance (PM), Predictive Maintenance (PdM), Calibrations, etc. Update equipment reliability plans based upon Root Cause Failure Analysis results to further reduce the number of failures and minimize the effects of failures that do occur. Perform root cause failure analysis of equipment deficiencies, develops, changes, and/or initiates maintenance activities such as PM, Condition Based Monitoring (CBM), lubrication programs, calibration, training, and spare parts strategies to improve performance and equipment availability. Based on investigation results, develop design modification projects to improve performance and initiates work orders or capital projects to complete. Provide input and oversight to equipment engineering standards. Provide maintenance engineering input to Capital Project Engineering through equipment selection review, PM / Calibration activity development, spare parts needs, and training requirements. Develop and implement plant safety improvements. Here Is What You Need (Minimum Requirements) Education: Degree in Engineering (Bachelor's or Master's) from an accredited institution Experience: 4+ years relevant experience with a BS degree in Engineering or 2+ years of relevant experience with an MS In Engineering. Language Skills: Excellent English reading, writing, speaking and communication skills required Relevant pharmaceutical experience, preferably in a sterile manufacturing facility Demonstrated time management skills, ability to work on multiple projects at a time Excellent interpersonal and communication skills with stakeholders, plant partners, engineers and maintenance technicians Demonstrated ability to effectively lead and build teams across functions and levels in the organization Bonus Points If You Have (Preferred Requirements): Certificates, Licenses or Registrations: Certified Maintenance and Reliability Professional (CMRP) (or equivalent) Proficiency in Computerized Maintenance Management Systems, preferably EAMS Solid background in Project Management Experience with regulatory compliance and quality standards in a pharmaceutical environment Strong analytical skills and attention to detail Ability to adapt to changing priorities and manage multiple tasks simultaneously Physical/Mental Requirements Frequent sitting, standing, walking required. Ability to perform mathematical calculations and perform complex data analysis required. The work environment ranges from office, to plant, to Maintenance shop. Colleague is frequently exposed to airborne particles and must work near moving mechanical parts. The noise level in the work environment is usually loud. Use of hearing, eye, hand and foot protection is required. Personal Protective Equipment applicable to the task must be worn at all times and is a condition of employment. Candidates must not be allergic to penicillin. Non-Standard Work Schedule, Travel or Environment Requirements Occasional travel may be required ( Other Details: Relocation support available Work Location Assignment: On Premise
The Manager, Reliability Engineering functions as part of an integrated team to provide Maintenance and Engineering support to on-going sterile injectable operation areas of the Rochester, MI plant. This position works directly with the area Maintenance Team Leader and is integrated with the team of craftsmen and enablers who support that same operating area of responsibility. General responsibilities are to provide the technical program leadership and implementation activities to maximize the maintenance-related uptime and operating efficiencies of equipment and facility assets. The Manager, Reliability Engineering is also responsible for optimizing Preventative Maintenance (PM) strategies and updating the associated planning and tracking systems. This position interacts extensively with the Operations Area in a business partner arrangement to achieve mutual production and uptime goals. The Manager, Reliability Engineering also functions as an integral team member and Subject Matter Expert to support Master Planning & Capital Project upgrades in the area of responsibility. The Rochester site is a penicillin manufacturing facility. Candidates must not be allergic to penicillin. What You Will Achieve In this role, you will: Work closely with Production and Project Engineering to target maintainability issues, lower maintenance costs, and implement improvements. Establish the initial preventive maintenance and calibration activities for equipment / instruments that are in accordance with the guidelines and specifications for that particular equipment / instrument class. Extend, deactivate, and/or update PM and Calibration activities through utilization of the PM / Calibration Optimization and Rationalization Program processes. Select the initial Maintenance Strategy for new equipment and provides updates to keep the strategy current. Implement equipment reliability plans by ensuring job plans and tasks are established for Preventative Maintenance (PM), Predictive Maintenance (PdM), Calibrations, etc. Update equipment reliability plans based upon Root Cause Failure Analysis results to further reduce the number of failures and minimize the effects of failures that do occur. Perform root cause failure analysis of equipment deficiencies, develops, changes, and/or initiates maintenance activities such as PM, Condition Based Monitoring (CBM), lubrication programs, calibration, training, and spare parts strategies to improve performance and equipment availability. Based on investigation results, develop design modification projects to improve performance and initiates work orders or capital projects to complete. Provide input and oversight to equipment engineering standards. Provide maintenance engineering input to Capital Project Engineering through equipment selection review, PM / Calibration activity development, spare parts needs, and training requirements. Develop and implement plant safety improvements. Here Is What You Need (Minimum Requirements) Education: Degree in Engineering (Bachelor's or Master's) from an accredited institution Experience: 4+ years relevant experience with a BS degree in Engineering or 2+ years of relevant experience with an MS In Engineering. Language Skills: Excellent English reading, writing, speaking and communication skills required Relevant pharmaceutical experience, preferably in a sterile manufacturing facility Demonstrated time management skills, ability to work on multiple projects at a time Excellent interpersonal and communication skills with stakeholders, plant partners, engineers and maintenance technicians Demonstrated ability to effectively lead and build teams across functions and levels in the organization Bonus Points If You Have (Preferred Requirements): Certificates, Licenses or Registrations: Certified Maintenance and Reliability Professional (CMRP) (or equivalent) Proficiency in Computerized Maintenance Management Systems, preferably EAMS Solid background in Project Management Experience with regulatory compliance and quality standards in a pharmaceutical environment Strong analytical skills and attention to detail Ability to adapt to changing priorities and manage multiple tasks simultaneously Physical/Mental Requirements Frequent sitting, standing, walking required. Ability to perform mathematical calculations and perform complex data analysis required. The work environment ranges from office, to plant, to Maintenance shop. Colleague is frequently exposed to airborne particles and must work near moving mechanical parts. The noise level in the work environment is usually loud. Use of hearing, eye, hand and foot protection is required. Personal Protective Equipment applicable to the task must be worn at all times and is a condition of employment. Candidates must not be allergic to penicillin. Non-Standard Work Schedule, Travel or Environment Requirements Occasional travel may be required ( Other Details: Relocation support available Work Location Assignment: On Premise