Protein Sciences Corp Posted November 6, 2026

Clean Utility Specialist / HSE Champion

Pearl River, United States Full time
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About this opportunity

Job Title: Clean Utility Specialist / HSE Champion

Location: Pearl River, NY

About The Job:

The Utilities Specialist - HSE Champion is responsible for Managing the Utilities operations and supporting the Health, Safety, and Environmental (HSE) initiatives at the Pearl River site. This role ensures compliance with regulatory and internal standards, supports critical utility systems, and fosters a strong culture of safety across all levels of the organization.

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:

Utilities Specialist Responsibilities

Provide technical and subject matter expert (SME) support for utility operations, including equipment troubleshooting and process issue resolution. Ensure systems operate in compliance with internal procedures and cGMP requirements.

Perform detailed root cause investigations for utility system and equipment failures. Define corrective actions and oversee implementation.

Develop and implement efficiency and reliability improvements.

Design, review, and maintain critical GMP documentation.

Create and modify preventive maintenance (PM) programs to ensure alignment with cGMP requirements.

Submit and manage work orders.

Submit and approve Safety Work Permits.

Monitor critical utility systems daily to ensure reliability and compliance.

Participate in after hours on call rotation

Provide logistics support as required.

HSE Champion Responsibilities

HSE Communications & Culture

Cascade monthly HSE updates, KPIs, audit results, and program changes.

Share best practices and lessons learned across departments.

Facilitate area-specific risk assessments and Job Hazard Analyses (JHAs).

Support site programs related to industrial hygiene, biosafety, fire and life safety, occupational safety, process safety, and environmental compliance.

Attend and actively participate in monthly HSE meetings.

Safety Program Management

Maintain and update JHAs and annual risk maps.

Coordinate product stewardship activities, including SDS updates and chemical inventory management.

Ensure compliance with medical surveillance requirements and task-based risk assessments.

Support regulatory compliance programs, including hazardous waste management, spill response, Aboveground Storage Tanks (ASTs), Lockout/Tagout (LOTO), and contractor safety.

Incident & Compliance Management

Initiate and manage accident and incident investigations within Qualipso.

Perform root cause analyses and ensure timely implementation of corrective and preventive actions (CAPAs).

Own and track action plans and ensure incidents are linked to relevant risk profiles.

Conduct internal audits and inspections to ensure compliance with applicable regulatory and corporate requirements.

Shop Floor Engagement

Lead Gemba walks and support Managing for Safety & Value (MSV) initiatives.

Support coactivity planning, permit-to-work processes, and emergency response drills, including fire, spill, MERT, and biohazard exercises.

Deliver onboarding and safety training for non-GMP areas.

Maintain and update safety maps and visual management tools.

Escalation & Continuous Improvement

Act as a liaison between area managers, HSE, and maintenance teams for escalations and issue resolution.

Identify, recommend, and escalate continuous improvement opportunities.

Monitor and trend key safety and performance metrics, including SRR, MSV, injury rates, and incident performance.

About You:

Basic Qualifications:

Education & Experience*

Bachelor's degree in Life Sciences, Pharmaceutical Sciences, Engineering, Safety Science, Occupational Health, Environmental Health & Safety, or a related technical discipline with 3+ years of experience in a pharmaceutical environment.

Associates degree in Engineering, Safety Science, Occupational Health, Environmental Health & Safety, maintenance or equivalent technical certification with 5+ years of experience in a pharmaceutical environment.

Highschool degree with 8+ years of experience in a pharmaceutical environment.

Certifications

Preferred: OSHA 30-Hour Certification (General Industry or Construction).

Technical Skills

Proficiency with Microsoft Office, Power BI, iObeya, Qualipso, and EHS Desk.

Familiarity with MSDS Online, SEDDA, and risk assessment tools.

Knowledge of chemical and biological safety principles is preferred.

Soft Skills

Strong communication, coaching, and interpersonal skills.

Excellent analytical and problem-solving abilities with strong attention to detail.

Ability to effectively lead cross-functional teams and influence stakeholders without direct authority.

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.

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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
Pearl River, 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

813 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 Not listed on this posting
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 $127,400)

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.