Job Title: Production Data & Process Support Specialist

Location: Pearl River, NY

About the Job

The Production Data & Process Support Specialist serves as the manufacturing-embedded expert for digital systems — primarily SAP (S/4HANA/iShift) and related ERP/MES platforms — ensuring that manufacturing personnel execute system transactions correctly, compliantly, and consistently in accordance with cGMP requirements. This role acts as the critical bridge between day-to-day manufacturing operations and the digital infrastructure that supports them, owning data quality and process integrity within the production environment.

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

SAP & iShift Systems Execution

Ensure manufacturing team members execute SAP transactions accurately, completely, and in full compliance with cGMP requirements and Sanofi's iShift core model standards
Serve as the primary manufacturing-embedded subject matter expert for SAP (S/4HANA) and iShift, providing real-time guidance and support to production personnel during daily operations
Monitor the accuracy and completeness of data entered into iShift and SAP; proactively identify data quality issues and take appropriate corrective action — either resolving directly within authorized scope or escalating through the proper channels (IT, Digital, or Master Data teams)

Training & Capability Development

Design and deliver training programs for manufacturing personnel on proper SAP transaction execution, iShift data entry protocols, and related digital workflows
Develop and maintain training materials, quick reference guides, and job aids to support consistent and compliant system usage across the manufacturing team
Serve as a change agent for digital adoption, coaching team members through system updates, process changes, and new iShift functionality rollouts

Data Governance & Quality

Own data quality monitoring within the manufacturing environment, establishing routines to review, validate, and correct production data in SAP and iShift
Collaborate closely with Master Data teams to ensure accurate, timely, and governance-compliant data management, including material master data, production orders, and batch records
Identify recurring data quality trends and escalate systemic issues with supporting documentation to appropriate stakeholders

Cross-Functional Coordination

Coordinate proactively with Supply Chain and Warehouse teams to ensure seamless data flow, process alignment, and timely resolution of interface issues between manufacturing and downstream functions
Triage and escalate system issues to IT, Digital, or Master Data teams as appropriate, providing clear documentation of the issue, business impact, and recommended resolution path
Participate in cross-functional meetings and working groups related to iShift operations, data governance, and manufacturing process alignment

Continuous Improvement & Documentation

Support and lead continuous improvement initiatives related to manufacturing data processes, identifying opportunities to streamline workflows, reduce errors, and improve data integrity
Maintain up-to-date standard operating procedures (SOPs) and work instructions for SAP and iShift system usage within the manufacturing environment
Contribute to post-go-live iShift stabilization and optimization efforts, serving as a key liaison between manufacturing operations and the Digital/iShift program team

About You

Bachelor’s degree
3+ years of experience in manufacturing operations, production support, or manufacturing systems roles within any GMP regulated industry
Demonstrated experience working with SAP (manufacturing or supply chain modules) and/or MES/ERP systems in a production environment
Proven track record of training or coaching others on system usage or process compliance

Technical Skills

Working knowledge of SAP manufacturing modules (e.g., PP, MM, WM) and/or SAP S/4HANA
Familiarity with digital manufacturing tools
Ability to identify, analyze, and resolve data discrepancies within ERP/MES systems

Regulatory & Compliance

Understanding of current Good Manufacturing Practice (cGMP) requirements and their application to data entry, batch records, and electronic systems in a pharmaceutical manufacturing environment
Awareness of data integrity principles (ALCOA+) as they apply to electronic systems

Interpersonal & Professional Skills

Strong analytical and problem-solving skills with the ability to make sound judgment calls on when to resolve vs. escalate issues
Excellent written and verbal communication skills; ability to translate technical system requirements into clear, actionable guidance for manufacturing personnel
Demonstrated ability to influence without authority and drive adoption of new processes or systems

PREFERRED QUALIFICATIONS

Experience with SAP S/4HANA or direct involvement in an iShift implementation or go-live support
Prior experience in pharmaceutical, biopharmaceutical, or vaccine manufacturing environments
Familiarity with master data governance processes, including material master creation/change request workflows
Experience with data integrity programs or quality management systems in a GMP-regulated environment
Lean, Six Sigma, or other continuous improvement training or certification
Experience supporting cross-functional teams spanning Supply Chain, Warehouse, and Manufacturing Operations

CORE COMPETENCIES / PROFICIENCY

Technical

Production Data Management / Advanced
Digital Technology / Advanced
Manufacturing Documentation / Intermediate
Safety Culture / Intermediate

Functional

Process Control / Experienced
Process Optimization / Experienced
Data Processing / Advanced
Process Improvements / Advanced

Transversal

Collaborative Communications / Experienced
Cross-Functional Teamwork / Mastered

Other

GMP Compliance / Advanced

PHYSICAL REQUIREMENTS & WORK ENVIRONMENT

Based at Sanofi's Pearl River manufacturing site
Regular presence on the production floor is required to provide in-person support to manufacturing personnel during operational hours
Office-based work for documentation, training development, and cross-functional coordination
Standard business hours with flexibility to support manufacturing operations as needed, which may include occasional off-shift or weekend coverage during system go-lives, critical issue resolution, or training events
Must comply with all site safety, gowning, and access requirements applicable to manufacturing areas

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; colour; 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:

$90.000,00 - $130.000,00

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.