Manager, Maintenance Engineer
Job Description
Why Patients Need You
Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what’s possible and taking action.
What You Will Achieve
Working with Pfizer’s dynamic engineering team, you will play a critical part in managing the maintenance and reliability engineering activities involving the redesign, maintenance, and repair of utilities systems, buildings, and production/non-production equipment.
As a Manager you will be responsible for providing technical and engineering expertise to maximize site equipment availability, reliability and reduce maintenance costs through system and process continuous improvement, i.e., LEAN principles and Continuous Improvement methodology. Develop and implement strategies and methods that improve preventive maintenance processes and procedures resulting in enhanced equipment performance. Technically support all aspects of maintenance operations while ensuring compliance with SOPs, cGMPs, safety procedures, quality standards, OSHA standards, other regulatory agency standards, good maintenance practices, and corporate initiatives. The successful candidate will be responsible for supporting the manufacturing processes and equipment at the Rochester site.
How You Will Achieve It:
A summary of responsibilities are following;
Work closely with manufacturing personnel/other departments to resolve manufacturing issues and implement process improvements.
Act as a liaison between manufacturing personnel and maintenance for corrective work and utilities support.
Support implementation of process equipment upgrades and optimization.
Capital projects for new bioprocess equipment purchase, installation and facility integration.
Trouble shooting issues with utility support of process equipment.
Coordination with other engineers, validation and automation colleagues in support of manufacturing operations.
Foster a Safety Culture
Fully Accountable for all assigned area Infrastructure Assets.
Plan and Forecast work required for assigned area Infrastructure Assets.
Provide development opportunities, cross-functional training, mentoring and diversity within Site Engineering & Maintenance
Provide good judgment and innovation by utilizing and adapting a broad knowledge of engineering principles and practices acquired through progressive experience.
Remain current in requirements of the ever changing business environment inclusive of site/network plan of record, capital budgeting and total cost of ownership including reliability.
Preparation of Capital Investment requirements to maintain assigned area’s Asset Reliability and Plan of Record.
Actively participate in or lead Site & Corporate initiatives such as Engineering Without Borders, Communities of Practice, Limited
Duration Teams, VPP, and Conformance Standards.
Perform equipment evaluations to determine and justify new equipment, equipment replacement and incorporate into capital plan. Equipment replacement should be identified as part of a site or facility Master Plan.
Review equipment for condition, performance, and maintenance history; assessing the liability caused by marginal equipment performance; assessing the cost and value of overhauling or upgrading to the cost of replacement; and creating justifications for capital replacements.
Equipment evaluations should include risk assessments to determine if adequate redundancy exists to support operations in the event of catastrophic equipment failure.
Recommends and presents capital equipment purchases to facilitate campus growth and to maximize equipment reliability.
Provide technical expertise to site investigations around Equipment/Utility Issues.
Provide subject matter expertise for PM task-list development and revisions. Assists RCM analysis team to determine PM and part strategies. Based on expertise, history, and RCM analysis results. Perform PM reviews, PM modifications, CMMS data mining to investigate equipment trends, failure defense identification and planning, work process improvements, and setup of maintenance metrics.
Programs and systems should be supported with procedures and training while ensuring compliance with all regulatory and company requirements.
Qualifications
Must-Have:
Applicant must have a HS Diploma (or Equivalent) with 10 years relevant experience, Or an Associate’s degree with 8 years’ experience; or a Bachelor’s degree with at least 5 years’ experience; or a Master’s degree with more than 3 years’ experience; or a PhD with 0-2 years’ experience.
Experience in any of the following disciplines: Construction Management, Biotechnology, Chemical Engineering, Mechanical Engineering, or equivalent science or engineering related discipline.
Nice-to-Have:
Direct knowledge and experience in project management within a biopharmaceutical or pharmaceutical cGMP environment.
Experience with FDA and EU licensing and inspection.
Familiarity with manufacturing and/or utilities equipment and operations.
Experience in both Global Engineering and site level engineering is strongly preferred.
Knowledge of Process Safety Management elements, especially Change of Design and Quality Assurance/Mechanical Integrity
Demonstrated skills in using a wide range of computer systems and software such as Microsoft Office Suite, reliability analysis software, and computerized maintenance management systems
Physical/Mental Requirements:
Leadership, organizational, and interpersonal skills.
Project management skills
Ability to communicate effectively across functions and levels in the organization. Oral and written communication skills.
Ability to shift priorities according to changes in departmental/facility needs.
Be highly motivated, show initiative, and work well independently or in a team environment.
Demonstrated ability to analyze equipment failures using personal knowledge and internal and external resources.
Prioritizing multiple commitments and technical problem-solving ability.
Non-Standard Work Schedule, Travel, or Environment Requirements:
Schedule is primarily day shift (M-F, 8 hrs), but at times it will be some off-shift support needed when issues arise.
Limited Travel
Other Job Details:
Last day to Apply: October 10th, 2024
Eligible for Relocation Assistance: Yes
Work Location Assignment:On Premise (On-site)
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.
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