Genz. Therap Product LP Posted November 5, 2026

Utilities Engineer

Framingham, United States Full time
Notify me about similar jobs

Genz. Therap Product LP 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 : Utilities Engineer

Location: Framingham, MA

About The Job:

The Utilities Engineer serves as technical owner and subject-matter expert for critical utility and facility systems supporting the MA BioCampus. Systems may include HVAC, high-purity water, clean and plant steam, compressed air and gases, chilled and heating water, building automation interfaces, and related campus infrastructure.

Working with limited supervision, you will ensure assigned systems remain safe, compliant, reliable, capable, and in a validated state of control. You will support manufacturing operations, maintenance, investigations, capital projects, shutdowns, commissioning, qualification, and regulatory inspections.

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 people’s lives.

Main Responsibilities:

Own the technical performance, capacity, reliability, compliance, and lifecycle strategy for assigned utility systems.

Monitor system performance, alarms, trends, sampling results, energy consumption, maintenance history, and emerging risks.

Lead complex troubleshooting and provide evidence-based assessments for failures, excursions, deviations, recurring alarms, and manufacturing interruptions.

Perform or review engineering calculations, equipment sizing, capacity evaluations, design reviews, and technical risk assessments.

Define maintenance requirements, acceptance criteria, post-maintenance testing, condition-monitoring activities, and critical-spare strategies.

Develop lifecycle plans and recommendations addressing equipment condition, obsolescence, redundancy, vendor support, and business-continuity risks.

Lead or support utility projects and modifications from requirements and design through implementation, testing, qualification, and turnover.

Own or support deviations, CAPAs, change controls, investigations, and effectiveness checks.

Maintain accurate, current, and inspection-ready drawings, specifications, calculations, system descriptions, and lifecycle records.

Support planned shutdowns, utility outages, start-ups, emergency response, restoration, and system return-to-service.

Identify opportunities to improve system reliability, energy efficiency, water consumption, sustainability, and lifecycle cost.

Manage technical vendors and provide guidance and mentoring to engineers and technical personnel.

Key Accountabilities:

Health, capacity, reliability, compliance, and lifecycle management of assigned systems

Manufacturing downtime attributable to the assigned equipment portfolio

Timely technical troubleshooting, risk assessment, and escalation

Successful delivery and turnover of assigned modifications and projects

Accurate deviation assessments, change controls, CAPAs, and technical documentation

Effective shutdown, contingency, restoration, and return-to-service planning

About You:

Basic Qualifications:

Bachelor’s degree in mechanical, chemical, electrical, environmental, or a related engineering discipline.

At least 3 years of engineering experience supporting utility, facility, manufacturing, or process systems.

Experience working in a regulated environment with knowledge of cGMP, OSHA, environmental, and engineering requirements.

Demonstrated expertise in one or more utility areas, such as HVAC, high-purity water, clean steam, compressed gases, plant steam, chilled water, or heating water.

Experience with engineering calculations, equipment sizing, troubleshooting, design reviews, project execution, and equipment lifecycle management.

Working knowledge of deviations, CAPAs, change control, commissioning, qualification, and maintenance strategies.

Strong problem-solving, technical-writing, project-management, collaboration, and communication skills.

Preferred Qualifications:

Three -Five or more years supporting pharmaceutical, biopharmaceutical, or similarly regulated manufacturing.

Experience with campus utilities, classified-space HVAC, high-purity water and steam, energy management, or business-continuity planning.

Familiarity with BMS, EMS, DCS/PLC interfaces, CMMS, data historians, and engineering drawing systems.

Knowledge of applicable ASME, NFPA, OSHA, EPA, ISPE, ASHRAE, and Good Engineering Practice standards.

Professional Engineer, Certified Energy Manager, PMP, Lean Six Sigma, or comparable certification.

Working Conditions:

Ability to access manufacturing, controlled, mechanical, utility, roof, and interstitial areas in accordance with safety and gowning requirements.

Availability to support a 24/7 manufacturing operation, including planned shutdowns, outages, start-ups, emergencies, and restoration activities as needed.

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 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-SG

#LI-GZ

#vhd

#LI-Onsite

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:

$100,500.00 - $145,166.66

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
Framingham, 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 $100,500/yr – $145,167/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
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Manufacturing & CMC job in the United States, and choose locations and companies.

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
40%
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.