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 Team leader, you will be involved in leading work teams within your division, including the technical and financial resources of the team. Thanks to your technical skills, you will coach your direct reports on day to day activities. You will be relied on to solve complex problems within your area of expertise.
It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
As a Sr Utilities Engineer (Clean Utilities), you will provide cross-functional support to operational teams for site GMP utilities. You will be setting priorities, forecasting, and allocating resources needed to complete all preventive and corrective maintenance tasks as well as providing areas of improvement for products, processes, or services. Through your comprehensive knowledge of principles, concepts, and theories of the discipline, you will also work towards advancing new concepts and methodologies.
This role is the site Subject Matter Expert (SME) for site GMP Clean Utilities infrastructure and systems (PW, WFI, Clean Steam, Pharmaceutical/Oil-Free Compressed Air, Process Gases, HVAC, etc.) and applications in aseptic manufacturing. In addition, the ancillary systems associated within their facilities. It has specific responsibility to participate over cross functional site improvements (design, construction, commissioning, qualification and start-up) of all GMP Utilities.
The Sr Utilities Engineer (Clean Utilities)will be responsible for effective, reliable, and cost-effective operation of the site’s GMP Utilities and ancillary systems associated within their facilities, maintaining all these systems in a state of compliance, in-control, and fit for use, capable of meeting all site needs. This role will also drive continuous improvement initiatives, cost saving and other department initiatives.
It is your dedication and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
Responsibilities may include:
Strong technical skills, be the Subject Matter Expert (SME) from equipment Utilities-HVAC systems. Deep technical expertise in all systems under his/her responsibility (GMP Utilities and ancillary systems associated within their facilities) and understanding their applications in pharmaceutical aseptic manufacturing.
You will provide technical SME support for mechanical, electrical, and pneumatic improvements or changes that impact utilities or utilities maintenance.
Promote, participate, and supervise the implementation and maintenance of the relevant safety programs in engineering department.
Support clean-black utilities equipment installation, qualification, start-up, PMs and coordinate vendors support as required.
Develop and modify procedures as needed to support clean-black utilities and HVAC systems.
Participate in clean utilities validation activities during project life cycle.
You will lead or support overall compliance requirements for the Utilities areas, including SOPs, change control, quality investigations and CAPAs.
To liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining, trouble shooting and installing / commissioning and service equipment.
Support the Production Operations in ensuring that utilities equipment is maintained to meet GMP requirements.
Support utilities areas in Regulatory / FDA inspections ensuring successful outcomes.
Cross functional collaboration with QC Micro, Operations, QA, Reliability, and other Engineering functional areas.
Ensure that all work is performed in accordance with standard operating procedures (SOPs), Current Good Manufacturing Practices (cGMP), safety procedures, quality standards, Occupational Safety and Health Administration (OSHA) standards, other regulatory agency standards, and good maintenance practices.
Support facilities, utilities, and infrastructure asset life-cycle replacement strategies and capital investment plans.
Support to develop andwrite equipment specifications, user requirement specifications, performance requirements, cost analysis, capital projects, change controls, and proposal for integrating new machinery-utilities into the site.
Schedules and coordinates adequate coverage for the department, depending on the business needs. Responsible to maintain an adequate inventory of spare parts of all critical utilities and facilities maintenance.
RM site operates 24/7, and the incumbent may be required to provide engineering support to Plant operations 24/7 as needed (overall facilities, utilities, equipment, etc.) and lead clean utilities shutdowns.
This is a key position, a technical advisor for the Engineering Department through teamwork and the formation of key alliances will drive, support, and implement key Plant projects and initiatives.
Ensures adherence to company safety standards, policies, and procedures. Ensures maintenance staff and contractors correctly wears and uses safety equipment, as required.
Also, ensures that all safety inspections are completed as required and ensures adherence to company EHS policies.
Qualifications
Must-Have
- Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience OR an associate's degree with 6 years of experience OR a bachelors with at least 3 years of experience OR Masters with more than 1 year of experience.
- Engineering experience in a Facilities, Utilities, Maintenance, Project, or Plant Engineering roles.
- Self-starter and have a proven track record in pharmaceutical facilities, clean-black utilities, equipment maintenance and troubleshooting.
- Experience in large facility and campus facility management and maintenance of buildings, building equipment and infrastructure.
- Hands-on experience in equipment upgrades and integration of new technology to improve plant facilities / central utilities operations.
- Required a thorough understanding of the operational processes of an organization and have a truly multidisciplinary role, working closely with colleagues across several functions in the site, including operations, maintenance, instrumentation, reliability, procurement, quality, technical services, validation, and project engineering.
- Demonstrated ability to interact effectively with contract service partners.
- Effective written and verbal communication skills.
Nice-to-Have
- Experience in WFI and HVAC systems, clean and black utilities.
- Excellent interpersonal, written, and verbal communication skills
- Demonstrated high level of understanding of engineering concepts, principles, and engineering functional standards.
- Technical aptitude and ability to train and mentor others.
- Engineering experience in the Pharmaceutical, Biotech or Medical Device industries.
- Experience with maintenance, reliability, and computerized maintenance management systems EAMS (CMMS)
- Strong Computer Skills:MS Project software applications, maintains up to date plant drawings.
PHYSICAL/MENTAL REQUIREMENTS
The work environment ranges from office to anywhere in the plant, on campus and frequently outdoors. Colleague is frequently exposed to airborne particles and must work near moving mechanical parts. Colleague will be expected to access multiple levels of the facility areas which entail use of stairways and ladders. The noise level in some of the work environments is 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
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
This role could require the support activities on-site that occur on evenings and weekends
Relocation support available
Work Location Assignment: On Premise
Last Day to Apply: November 25, 2024
The annual base salary for this position ranges from $78,000.00 to $130,000.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.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.
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