Protein Sciences Corp Posted October 21, 2026

Manager, GMP Facility, Asset Readiness & HSE

Pearl River, United States Full time
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About this opportunity

Job Title: Manager, GMP Facility, Asset Readiness & HSE

Location: Pearl River, NY

About the Job:

Leads GMP facility readiness, equipment asset care, and HSE compliance to ensure the manufacturing shopfloor is maintained in a GMP-ready and safety-ready state at all times. Oversees GMP cleaning operations, manages two dedicated maintenance technicians for asset care, and partners with Maintenance teams on equipment PM, calibration, and shutdown planning. Dedicates 25-50% of time to HSE activities including safe work practices, 5S implementation, work permitting, and safety compliance. Ensures attention to facility details including rust, cleaning residue, paint integrity, and floor conditions while maintaining all GMP documentation and environmental monitoring requirements.

Leads GMP facility readiness, equipment asset care, and HSE compliance to ensure the manufacturing shopfloor is maintained in a GMP-ready and safety-ready state at all times. This role is accountable for facility cleanliness, equipment reliability, asset care management, and health, safety & environment compliance across all manufacturing operations.

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:

GMP Facility & Cleaning Operations

Ensure the manufacturing facility is maintained in a GMP-ready and safety-ready state at all times

Oversee and coordinate GMP cleaning operations of all manufacturing areas in compliance with cleaning procedures and validation requirements

Partner with third-party cleaning contractor to ensure thorough execution of cleaning activities, with attention to detail including rust, cleaning residue, paint integrity, floor conditions, and other facility deficiencies

Conduct regular facility walkthroughs to identify and remediate GMP and safety deficiencies

Maintain cleaning logs, records, and documentation in compliance with GMP requirements

Ensure environmental monitoring requirements are supported and met within the manufacturing facility

Equipment Asset Care & Maintenance

Directly manage two dedicated maintenance technicians focused on asset care and equipment readiness

Ensure all manufacturing equipment is clean, calibrated, and current with preventive maintenance (PM) schedules

Partner with the Maintenance team to define scope of work, planning, and execution of maintenance shutdowns

Maintain equipment status boards and asset care records to ensure full traceability and GMP compliance

Proactively identify equipment reliability risks and drive resolution through appropriate channels

Support equipment qualification activities (IQ/OQ/PQ) and change control processes as needed

Health, Safety & Environment (HSE), 25–50% of Role

Champion a culture of safety across the manufacturing shopfloor

Ensure safe work practices are understood, followed, and reinforced among all team members and contractors

Manage and coordinate work permitting processes (e.g., confined space, hot work, lockout/tagout)

Lead and sustain 5S implementation and continuous improvement across manufacturing areas

Conduct safety walkthroughs, hazard assessments, and near-miss investigations

Ensure compliance with all applicable HSE regulations, site policies, and Sanofi standards

Serve as a key point of contact for HSE topics on the manufacturing shopfloor

Team Leadership & Collaboration

Lead, develop, and manage two dedicated asset care maintenance technicians

Collaborate cross-functionally with Maintenance, Quality, and Manufacturing teams

Coordinate with cleaning contractor management to ensure GMP and safety standards are consistently met

Participate in deviation investigations related to facility, equipment, or cleaning deficiencies

Support regulatory inspections and internal audits related to facility and equipment readiness

Technical Knowledge

Working knowledge of cGMP regulations (21 CFR Parts 210, 211) and GMP cleaning requirements

Understanding of environmental monitoring principles and practices in a manufacturing setting

Knowledge of preventive maintenance, calibration programs, and equipment qualification

Experience with 5S implementation and workplace organization

Familiarity with work permitting systems and HSE compliance requirements

Soft Skills

Strong attention to detail and commitment to GMP and safety standards

Proactive problem-solving and facility management skills

Effective leadership and team development capabilities

Strong communication and cross-functional collaboration skills

Ability to manage multiple priorities in a fast-paced manufacturing environment

Continuous improvement mindset with hands-on approach

Physical Requirements

Ability to work in a manufacturing environment including cleanroom gowning requirements

Regular walking and standing during facility inspections and shopfloor activities

Occasional lifting up to 35 lbs

Flexibility to respond to facility or equipment issues outside of standard business hours

About You:

Basic Qualifications

Bachelor's degree

2+ years of experience in a GMP-regulated environment (biopharmaceutical, pharmaceutical, medical device/combination product manufacturing, or any related)

Demonstrated experience managing facility readiness, equipment maintenance, or asset care programs

Proven experience implementing and sustaining 5S methodology in a manufacturing environment

Experience coordinating with maintenance teams and/or third-party contractors

Familiarity with HSE programs including safe work practices, permitting, and safety compliance.

Preferred Qualifications

Experience in vaccine, biologics, or recombinant protein manufacturing

OSHA 30-hour certification or equivalent HSE training

Experience managing third-party cleaning or maintenance contractors

Knowledge of cleaning validation principles

Lean Manufacturing or Six Sigma training

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:

$78.000,00 - $112.666,66

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
Manager
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 661 comparable Manager Manufacturing & CMC roles across 87 biopharma companies.

661Comparable roles tracked
594Currently active
87Companies hiring similar roles
41Countries represented

Salary context

205 of 661 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Warehouse Associate I (M-F 11am-7:30pm) · AbbVie $16/hr – $29/hr (≈ $33,280–$60,320/yr)
Highest disclosed · Regional Manager - Megasys · Merck KGaA $220,000/yr – $250,000/yr
Peer group range $46,800 – $235,000 (median $156,390)

Where these roles are based

Top locations among the 661 comparable roles

United States372
India58
Ireland23
Japan21
Netherlands21
United Kingdom20

+ 35 more countries

Seniority mix

661 of 661 peers have a known seniority level

Manager380
Associate162
Associate Director119

Therapeutic area mix

9 of 661 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease5
Rare Disease3
Immunology1

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.

60%similar
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Renss, United States Manager
Same function Same seniority Same country
60%similar
RayzeBio, Inc Indianapolis, United States Manager
Same function Same seniority Same country
60%similar
RayzeBio, Inc Indianapolis, United States Manager
Same function Same seniority Same country
60%similar
Devens Devens, United States Manager
Same function Same seniority Same country
60%similar
Devens Devens, United States Manager
Same function Same seniority 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.

60%
Senior Manager, Site SAP Business Lead
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
60%
Senior Manager, Radiopharmaceutical Development/CMC
RayzeBio, Inc · Indianapolis, United States · Manager
Function Therapeutic area Seniority Country
60%
Senior Manager, ECQ Delivery
Celgene - Summit (Corp) · Summit West, United States · Manager
Function Therapeutic area Seniority Country
60%
Front Line Manufacturing Manager - Bulk Drug Substance Services - Days
Amgen Inc. · Holly Springs, United States · Manager
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.