Sanofi Vaccines US Inc. Posted November 6, 2026

Reliability & Methods Engineer

Swiftwater, United States Full time
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Sanofi Vaccines US Inc. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Title: Reliability & Methods Engineer

Location: Swiftwater, PA

About the Job

The Reliability Engineer is a critical technical role under the Reliability & Engineering Manager pillar, responsible for ensuring the reliability, availability, and compliance of equipment across our manufacturing operations. You will serve as a technical expert in reliability engineering, driving data-driven maintenance strategies, root cause investigations, and continuous improvement initiatives that enable our teams to deliver high-quality medicines to patients without interruption.

Join a global network that powers how Sanofi delivers, seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve lives.

Main Responsibilities

In this role, you will take ownership of the reliability performance of production equipment and systems across the site. You will develop and execute reliability-centered maintenance (RCM) strategies, optimize preventive and predictive maintenance programs, and lead failure analysis efforts (RCA, FMEA) to reduce unplanned downtime, minimize product loss, and improve overall equipment effectiveness (OEE).

You will use SAP (PM/EAM) data, equipment performance metrics, and maintenance history to identify trends, quantify losses, and prioritize improvement opportunities. You will partner closely with Manufacturing, Maintenance, Quality, Validation, and Engineering to implement sustainable fixes, support equipment changeovers and modifications, and ensure that all changes are executed in compliance with GMP and change control requirements.

You will also manage OEM and vendor technical relationships, support spare parts strategy and criticality assessments, and contribute to capital projects and equipment upgrades. As a key contributor to Sanofi's operational excellence and digital transformation initiatives, you will help ensure our manufacturing operations are robust, compliant, and ready for the future.

Reliability Engineer

Position Overview: Reliability Engineer responsible for the performance, availability, and lifecycle management of production equipment and systems, ensuring compliance with GMP and quality standards.

Key Responsibilities:

Develop, implement, and continuously improve reliability strategies, including RCM, FMEA, criticality assessments, and equipment strategy optimization.

Lead root cause analysis (RCA) for equipment failures, deviations, and chronic losses; define and track corrective and preventive actions (CAPA).

Optimize preventive and predictive maintenance programs and PM task lists in SAP to improve MTBF, MTTR, and OEE.

Analyze equipment performance data (downtime, minor stops, changeover, rejects) to identify improvement opportunities and quantify business impact.

Partner with Maintenance, Manufacturing, Quality, and Validation teams to support startups, changeovers, equipment modifications, and qualification activities.

Manage OEM and vendor technical relationships, including service support, upgrades, obsolescence planning, and technical troubleshooting.

Define and manage critical spare parts strategy, including min/max levels, criticality, and obsolescence risk.

Author and review technical documentation, including SOPs, work instructions, change controls, deviations, and engineering reports.

Support capital projects, equipment upgrades, and technology transfers.

Interface with site leadership, Finance, and Procurement on maintenance budgeting, cost tracking, and spend justification.

About You

Basic Qualifications

Bachelor's degree.

3+ years of experience in engineering and maintenance of production equipment in a GMP-regulated environment.

Proven experience with reliability engineering methodologies (RCA, RCM, FMEA, failure analysis, OEE).

Experience with SAP (PM/EAM) and maintenance data analysis.

In-depth knowledge of engineering and maintenance principles in pharmaceutical manufacturing processes, including technical knowledge of process equipment and automated mechanical systems.

Ability to read, create, and interpret mechanical drawings, P&IDs, electrical schematics, technical documentation, and PLC/HMI documentation.

Familiarity with pharmaceutical regulations, including cGMP, FDA, EU Annex 1, and ISO standards.

Excellent analytical and problem-solving skills to address complex technical issues.

Excellence in cross-functional collaboration, leadership, and technical communication.

Financial acumen related to maintenance budgeting, cost tracking, and procurement.

Desired Skills:

Hands-on experience with Inova/ Optima filling equipment (operation, maintenance, troubleshooting, or engineering support).

Familiarity with aseptic processing equipment, isolator/RABS technology, and aseptic intervention principles.

Knowledge of predictive maintenance and condition monitoring technologies (vibration, thermography, data analytics).

Experience with CMMS/EAM, data visualization tools (Power BI, Spotfire), and Lean/Six Sigma methodologies.

Understanding of spare parts management and procurement workflows.

Project management experience, including capital project execution.

Experience with SAP S/4HANA and Fiori applications.

Preferred Certifications: CMRP, CRE, Six Sigma Green/Black Belt, or equivalent.

Core Competencies:

Technical expertise in production equipment and reliability engineering

Quality- and compliance-focused mindset

Analytical and structured problem solving

Process improvement orientation

Strong communication and influencing skills

Training and knowledge-sharing capabilities

Change management proficiency

This position plays a crucial role in ensuring the reliability and compliance of our manufacturing operations, directly supporting Sanofi's commitment to supply continuity and operational excellence for patients worldwide.

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.

Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.

Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale

Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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.

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Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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.

North America Applicants Only

The salary range for this position is:

$85,500.00 - $123,500.00

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.

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Swiftwater, United States
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3428 comparable Manufacturing & CMC roles across 175 biopharma companies.

3428Comparable roles tracked
3174Currently active
175Companies hiring similar roles
61Countries represented

Salary context

812 of 3428 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject $85,500/yr – $123,500/yr
Lowest disclosed · Operator – Plant Utilities · Lilly $13/hr – $28/hr (≈ $26,998–$58,302/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $42,650 – $381,150 (median $127,500)

Where these roles are based

Top locations among the 3428 comparable roles

United States1570
Germany211
India155
France149
Ireland129
China125

+ 55 more countries

Seniority mix

1516 of 3428 peers have a known seniority level

Senior408
Manager359
Intern/Fellow/Postdoc208
Associate149
Principal129
Associate Director105
Director104
Senior Director48
Executive/VP6

Therapeutic area mix

22 of 3428 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease13
Rare Disease3
Dermatology & Aesthetics2
Oncology2
Immunology1
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
40%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same country
40%similar
Merck West Point, Pennsylvania, United States of America Principal
Same function Same country
40%similar
Merck West Point, Pennsylvania, United States Intern/Fellow/Postdoc
Same function Same country
40%similar
AbbVie North Chicago, IL Associate Director
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Notify me about similar jobs

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Director, Global Regulatory Affairs – Chemistry, Manufacturing and Controls (CMC), Platform Innovation – Synthetic Peptides and Oligonucleotides
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Associate Principal Scientist/Engineer, Medical Device and Combination Products, Analytical
Merck · West Point, Pennsylvania, United States of America · Principal
Function Therapeutic area Seniority Country
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Senior Scientist II - Biologics Drug Product Development
AbbVie · North Chicago, IL · Senior
Function Therapeutic area Seniority Country
40%
Senior Scientist, II Biologics & Genetic Medicine - LCMS Characterization & Bioanalysis
AbbVie · North Chicago, IL · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.