
Manufacturing GDP Specialist
Pearl River, NYFull-time$59–85K/yrSeen 6 days agoSeen in employer's feed 6 days ago
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Job overview
The Manufacturing GDP Specialist ensures manufacturing documentation integrity and compliance by reviewing batch records and logbooks, tracking errors, and supporting timely corrections. The role coaches shopfloor personnel on Good Documentation Practices, escalates documentation issues, and contributes to deviation investigations, CAPA development, audits, and batch record simplification. It works with Manufacturing, Quality, and shopfloor teams to support documentation accuracy and quality across manufacturing operations.
Skills & qualifications
Skills
Qualifications
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Full job description
Pearl River, NY
Full time
R2875512
Job Title: Manufacturing GDP Specialist
Location: Pearl River, NY
About the Job:
Ensures the integrity and compliance of manufacturing documentation by tracking, reviewing, and correcting batch records and logbooks in accordance with Good Documentation Practices (GDP) and applicable regulatory requirements. Partners closely with Manufacturing Technicians to drive timely error correction, maintains error tracking metrics to identify and resolve repeated GDP violations, and coaches shopfloor personnel on GDP principles. Plays a key role in safeguarding the safety, efficacy, and quality of drug substance by identifying and escalating GDP-related issues, supporting batch record simplification efforts, and contributing to deviation investigations and CAPA development.
This role is accountable for documentation accuracy, batch record review cycle time, and fostering a culture of quality and compliance across 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:
Batch Record & Logbook Review
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Track and review manufacturing batch records and logbooks to ensure compliance with GDP and regulatory requirements
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Follow up with Manufacturing Technicians to ensure corrections are completed in a timely manner
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Ensure batch record review cycle time targets are consistently met
Error Tracking & Continuous Improvement
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Maintain error tracking metrics to identify, address, and correct repeated violations of GDP
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Review batch record structure and recommend simplifications to minimize errors, as applicable
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Coach shopfloor technicians on GDP principles and best practices
Quality & Compliance Escalation
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Identify and escalate GDP issues that could affect the safety, efficacy, and quality of drug substance
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Participate in deviation investigations and CAPA (Corrective and Preventive Action) creation, as applicable
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Support regulatory inspections and internal audits related to documentation practices
Team Collaboration
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Collaborate cross-functionally with Manufacturing, Quality, and shopfloor teams
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Serve as a key point of contact for GDP-related questions and guidance on the shopfloor
Physical Requirements
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Ability to work in a manufacturing environment, including cleanroom gowning requirements
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Regular walking and standing during shopfloor reviews and interactions with Manufacturing Technicians
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Occasional lifting up to 25 lbs
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Flexibility to respond to documentation or compliance issues outside of standard business hours, as needed
About You:
Basic Qualifications
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High school diploma or equivalent.
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1+ years of experience in a GMP regulated manufacturing environment.
Preferred Qualifications
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Associate or bachelor's degree in a science, engineering, or related field
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Prior experience in biopharmaceutical, pharmaceutical, or vaccine, biologics, or equivalent industries.
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Exposure to electronic batch record (EBR) systems
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Lean Manufacturing or continuous improvement training
Technical Skills
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Working knowledge of Good Documentation Practices (GDP) and cGMP regulations (21 CFR Parts 210, 211)
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Familiarity with batch record review and manufacturing logbook requirements
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Understanding of deviation investigation and CAPA processes, a plus
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Basic knowledge of error tracking and metrics reporting tools (e.g., Excel, electronic batch record systems), a plus.
Soft Skills:
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Highly detail-oriented with the ability to work quickly and accurately
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Sound interpersonal and information-gathering skills
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Ability to work effectively in a team environment and interact with others across all levels
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Strong written and verbal communication skills
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Proactive, quality-focused mindset
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Demonstrated attention to detail and accuracy in documentation-focused tasks
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Ability to work quickly and accurately under time constraints
Why choose us?
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Bring the miracles of science to life alongside a supportive, future-focused team.
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Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
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Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
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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.
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Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
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Power industry-leading performance by leveraging digital, data, and AI-driven innovation at speed and scale
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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 (https://cscontactus.sanofi.us/accessibilityQuestionComments.aspx)
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:
$58.500,00 - $84.500,00
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.
We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting www.sanofi.com or via our movie We are Sanofi (https://youtu.be/96EwNjb1TLo)
Start a career that makes a difference.
Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies. Whether it’s using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.
How this job compares
Set against the 2,789 open Compliance jobs on Olive Jobs, counted November 6, 2026.
- Pay
- This posting$59–85K/yr
- New York median$120–175K/yr237 salary ranges
- US median$113–175K/yr1,907 salary ranges
This range's midpoint, $72K, is 52% below the New York median midpoint ($150K) — in the lowest quarter of Compliance salary ranges in New York.
- Openings
- Olive Jobs lists 333 open Compliance jobs in New York and 2,789 across the US. 8% of them nationwide are listed as remote or flexible.
- Hiring the most in New York
- Capital One10 open
- City of New York10 open
- JPMorgan Chase10 open
- Experience
- This posting asks for at least 1 year of experience — less than three in four Compliance postings that state a minimum ask for (median 5 years, across 2,400 postings).
- Education
- This posting asks for a high school diploma; 1,465 of the 2,789 open Compliance jobs (53%) ask for a high school diploma or higher.
Counted across the open, public US postings on Olive Jobs on November 6, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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