
Manufacturing and Supply
Wo Wunder der Wissenschaft
für Patient*innen Realität werden
Clean Utilities Engineer
Auf einen Blick:
Unsere Teams produzieren und liefern jedes Jahr über 4 Milliarden Einheiten an Medikamenten und Impfstoffen und sorgen dafür, dass jede Innovation die Menschen erreicht, die sie am dringendsten benötigen. Unsere hochmodernen Produktionsstätten, KI-gestützten Smart Factories und wegweisenden Automatisierungstechnologien setzen neue Maßstäbe – damit Behandlungen Patient*innen schneller, sicherer und nachhaltiger als je zuvor erreichen. Hier kannst Du mit Deinen Fähigkeiten, Deinen Ambitionen und Deiner Leidenschaft die Zukunft des Gesundheitswesens mitgestalten.
Job title: Clean Utilities Engineer
Location: Swiftwater, PA
Note: Candidates must be available 40 hours per week, Monday-Friday
About the Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Our Team/ Overview
The Clean Utilities Engineer will be responsible for leading design and managing clean and site utility Tier III projects at the SWR site, along with routine M&S process support. This position will be responsible for working with other Engineering and Project Management teams as a Subject Matter Expert (SME) for Clean utilities.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Accountabilities:
The Clean Utilities Engineer is responsible for successful delivery of Clean and Plant Utilities portions of Tier III and Infrastructure projects (approx. $0M to $5M value), helping to manage contractors and set site design standards in accordance with Sanofi Global standards and Swiftwater site norms. Additionally, responsibilities include troubleshooting issues of concern with GMP and Plant Utility Systems and associated equipment. Efforts include walkdowns of equipment and piping systems (GEMBA) and assistance with deviations and change controls as required. The Clean Utilities engineer will be responsible for managing design, cost, schedule, construction, safety, quality, commissioning, qualification and validation activities on both projects and site process support for applicable scope in an effective manner in accordance with Sanofi Project Management policies & procedures to meet committed project objectives. Scope includes projects involving both new, and modifications to existing equipment, process, utilities, buildings and infrastructure systems, site audit support, and a key input to Site Master Planning.
Main Responsibilities:
Provide input and engineering to support decision making processes with site leadership team and central process function.
Establish strategic relationships with key stakeholders. Support Site Leadership Team (SLT) and the Compelling Business Needs (CBNs) by ensuring alignment of workloads with company priorities. Frequent collaboration/presentation with senior level SWR and Global Sanofi Management is required. Act as the liaison into regional project execution programs and support with resourcing and expertise when requested.
Advising on strategies to ensure all utilities engineering activities comply with industry regulations and standards
Implementing process improvements to enhance efficiency, safety, and quality within the engineering and maintenance groups
Emphasis on implementation of projects in a safe and GMP compliant manner. Meet all HSE training requirements, and implement HSE procedures (Safe Plan of Actions, Permits, Pre-Startup Safety Review, HSE checklist, etc.) on all projects. Assure compliance with Quality requirements as defined by applicable Sanofi Quality Standards, site procedures, and by Change Control requirements.
Provide input for selection and management of external contractors and suppliers to ensure they meet the company’s standards and requirements.
The Clean Utilities Engineer will be expected to understand and use key Sanofi systems including electronic document management tools, Qualipso, Bluecielo, etc., and must have experience supervising engineering design, conducting structured project reviews, supervising construction activities, managing cost and schedule, tracking Progress, planning and coordinating C&Q activities, coordinating with maintenance for calibration and turnover activities, managing CAD and technical documentation turnover, and coordinating with other stakeholders and functions during execution.
The Clean Utilities Engineer must be comfortable working in GMP Process and industrial settings. Providing “hands-on” inspections of equipment and piping systems and providing engineering insight into the operations and design of these systems.
The Clean Utilities Engineer will be responsible for working with contractors and other team members to assure that all systems, in the scope of responsibility, are constructed in accordance with relevant specifications and Sanofi standards, and that all relevant turnover documentation is supplied in a compliant and timely manner. Startup and commissioning of new or modified systems is essential as well as working with the C&Q team members to assure that systems can be qualified per Sanofi and cGMP standards.
Related KPIs & Metrics:
HSE performance (Injury Rates, Near Misses, Potential Serious Injuries (PSI))
On time, on budget delivery of representative systems while adhering to strict quality and regulatory standards and specifications.
Represent Clean Utilities systems during inspections and audits.
Impact on Business Outcomes of M&S
About You
Education & Experience & Certifications:
Excellent leadership, communication, and cross-functional collaboration skills
Technical Expertise (In-depth knowledge of engineering & maintenance principles on pharmaceutical manufacturing processes)
Technical knowledge of process equipment, understanding of automated mechanical systems and the ability to create and interpret technical documentation.
Regulatory Knowledge (Familiarity with pharmaceutical industry regulations, including GMP, FDA, & ISO standards)
Problem-Solving (Excellent analytical and problem-solving skills to address technical issues.)
Minimum B.S., Engineering Degree and/or Equivalent Science/Technical Degree with experience relevant to life sciences and/or vaccines manufacturing.
Minimum 5-10 years’ experience in engineering & maintenance of Clean Utilities systems, supporting small to medium capital projects. Demonstrated experience with GMP requirements, engineering design, construction, project controls (including cost control and scheduling), commissioning, qualification and validation activities.
Physical Requirements & Special Working Conditions:
N/A
Key Involvement in Decision-Making Process:
Key Roles (D,A,I)
Capital Project Approvals (A)
Project < 5M€ (D) and Project > 5M€ (A)
Regulatory Compliance Strategies (A)
Process Improvement Initiatives (A)
Vendor Selection and Management (D)
Local specificities
Additional Accountabilities:
N/A
Disclaimer
The above information was designed to indicate the general nature and level of work performed by employees with this job description. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Requirements are subject to possible modification to reasonably accommodate qualified individuals with disabilities. This document does not create an employment contract, implied or otherwise, other than an “at will” employment relationship.
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants
will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic
partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability
for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or
any other characteristic protected by law.
#GD-SP
#LI-SP
#vhd
#LI-Onsite
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Strebe nach Fortschritt. Entdecke Einzigartiges.
Werde Teil von Sanofi und starte mit uns in eine neue Ära der Wissenschaft – wo dein persönliches Wachstum genauso wegweisend ist wie unsere Arbeit. Wir investieren in dich, damit du weiterkommst, schneller denkst und Dinge möglich machst, die vorher undenkbar waren. Du wirst Grenzen verschieben, Gewohntes hinterfragen und smarte Lösungen entwickeln, die direkt bei den Menschen ankommen, für die wir da sind. Bereit, die Wunder der Wissenschaft zu jagen und Leben zu verbessern? Dann lass uns gemeinsam Großes bewegen – und das Außergewöhnliche entdecken.
Bei Sanofi stehen allen die gleichen Chancen offen – unabhängig von Herkunft, Hautfarbe, Religion, Geschlecht, Nationalität, sexueller Orientierung, Alter, Staatsangehörigkeit, Familienstand, Behinderung, Geschlechtsidentität, Veteranenstatus oder anderen gesetzlich geschützten Merkmalen.

Mehr Informationen über diesen Standort

Warum bei uns arbeiten?
- Wir stellen nicht nur Medikamente her – wir bewirken etwas. Unser globales Netzwerk modernster Produktionsstätten sorgt dafür, dass Patient*innen die Behandlungen erhalten, die sie brauchen – genau zur richtigen Zeit.
- Innovation treibt uns an. Von KI-gestützter Fertigung bis hin zu weltweit führenden Produktionsmethoden setzen wir neue Maßstäbe in Effizienz und Leistung.
- Hier wachsen Karrieren. Ob in der Produktion, Qualitätssicherung, Ingenieurtechnik oder in der Supply Chain– arbeitest Du mit erstklassigen Talenten zusammen, entwickelst Deine Fähigkeiten weiter und gestaltest die Zukunft der Pharmaindustrie mit.
- Wir tun, was richtig ist. Sicherheit, Nachhaltigkeit, Vielfalt, Gleichberechtigung und Inklusion stehen im Mittelpunkt unseres Handelns – für ein Arbeitsumfeld, in dem alle erfolgreich sein können.
All-In für Vielfalt
Bei Sanofi führen unterschiedliche Perspektiven zu den besten Lösungen für Patient*innen. Erfahre von Monique Vessey, unserer Leiterin der Supply Chain -Transformation, wie ihre persönliche Geschichte ihre Arbeit bei der Bereitstellung lebenswichtiger Medikamente prägt.

"Manufacturing & Supply bildet die Brücke zwischen der Wissenschaft in unseren Forschungslaboren und den Menschen und Gemeinschaften, die wir versorgen."

Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
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