Reliability Engineer

Job Description Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com. The Reliability Engineer supports equipment, utilities, and manufacturing systems within Agilent's pharmaceutical API manufacturing sites. This role executes and advances equipment reliability strategies, conducts failure analysis, drives preventive and predictive maintenance programs, and develops asset lifecycle plans to ensure maximum equipment availability and cGMP compliance. Responsibilities include authoring and approving reliability documentation, supporting investigations, developing risk mitigation strategies, and providing technical guidance to cross‑functional teams. All duties require strict adherence to cGMP and regulatory expectations.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Develops and maintains reliability programs, including preventive and predictive maintenance strategies for manufacturing and facility equipment. Authors and approves reliability-related documentation, including maintenance plans, equipment lifecycle assessments, and reliability studies. Performs root cause analysis (RCA), statistical analysis, and failure mode and effects analysis (FMEA) to reduce equipment downtime and improve system performance. Supports investigations, deviations, and CAPAs related to equipment failures, maintenance issues, or reliability events. Partners with Engineering, Maintenance, Facilities, Manufacturing, and Quality Assurance to ensure reliability strategies align with site and corporate objectives. Implements data‑driven improvements for equipment performance, availability, and maintainability. Identifies and leads continuous improvement initiatives targeting uptime, cost reduction, and asset optimization. Provides subject-matter expertise on reliability engineering methodologies, tools, and industry best practices. Ensures all maintenance and reliability programs comply with cGMP guidelines and applicable regulatory requirements. Supports the introduction of new equipment, including reliability risk assessments, maintenance planning, spare parts strategies, and training. Represents the reliability program during internal and external audits. Develops technical reports, maintenance plans, and documentation aligned with corporate engineering and industry standards. Evaluates issues from diverse perspectives (safety, compliance, process, equipment, and human factors) to implement durable corrective actions. Maintains alignment with internal stakeholders on reliability goals, KPI metrics, and implementation of engineering standards. Assists with risk assessments, equipment criticality assessments, and reliability planning activities for new or existing manufacturing systems. Assists with facility master planning, including asset lifecycle assessments and asset re-capitalization plan. Qualifications Bachelor's or Master's Degree in Engineering (Mechanical, Chemical, Electrical, Industrial), Science, or related field—or equivalent education and experience. 4+ years practical experience, with at least 3+ years in reliability engineering, maintenance engineering, or related field. Requires in‑depth knowledge and experience and the ability to work independently. Ability to perform essential duties satisfactorily and meet quality and safety requirements. Strong ability to analyze and interpret engineering data, technical documents, and scientific publications. Proficient in reliability engineering tools such as RCA, FMEA, Weibull analysis, failure diagnostics, or condition-based monitoring. Strong writing and communication skills, with the ability to convey technical information to cross‑functional audiences. Working knowledge of pharmaceutical manufacturing processes, reliability best practices, and quality system requirements. Ability to apply engineering principles to solve complex problems, collect and interpret data, and draw valid conclusions. Experience with maintenance management systems (e.g., CMMS), reliability software, or statistical tools preferred. Ability to manage multiple priorities, meet deadlines, and balance long‑term reliability initiatives with immediate operational needs. Knowledge of cGMP guidelines and international regulations related to API or drug product manufacturing. Demonstrated technical competence and ongoing engagement in the field of reliability engineering. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least April 17, 2026 or until the job is no longer posted. The full-time equivalent pay range for this position is $103,200.00 - $161,250.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.

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Manufacturing Graduate and Student Career Site Visit our career site and learn more about Agilent Watch our video playlist to get a glimpse of life at Agilent! As a global leader in laboratory and clinical technologies, we are passionate about bringing great science to life. Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. Leveraging more than 50 years of expertise, we create advanced instruments, software, and consumables supported by teams of highly skilled and knowledgeable people. With 18,000 employees around the world, our global reach and comprehensive solutions provide the most reliable and accurate results, as well as optimal scientific, economic, and operational outcomes. We work collaboratively with our customers on their journey to make a real difference in human lives. Our culture is founded on trust, respect, and uncompromising integrity, and we pride ourselves on being a dynamic and inclusive workplace that celebrates diversity and fosters innovation. We can't wait for you to join us as we continue our mission to improve the world around us. Information about Agilent is available at Agilent.com.