Manufacturing GDP Specialist

Sanofi; Pearl River (NY); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health benefits

Parental leave

Career development

Job summary

Sanofi Pearl River, NY is seeking a Manufacturing GDP Specialist to ensure the integrity and compliance of manufacturing documentation by reviewing batch records and logbooks in line with GDP and regulatory requirements. You will partner with Manufacturing Technicians to drive timely corrections and maintain error-tracking metrics.

The role focuses on safeguarding drug substance quality, supporting batch record simplification, and contributing to deviation investigations and CAPA development.

Qualifications

• GDP and cGMP knowledge is required.
• Experience with GMP manufacturing environments is preferred.
• Familiarity with batch record review and deviation investigations is a plus.

Responsibilities

• Review and correct batch records and logbooks to ensure GDP/regulatory compliance.
• Collaborate with Manufacturing Technicians to ensure timely corrections.
• Identify and escalate GDP issues; participate in CAPA and deviation investigations.

Skills

Attention to detail

Team collaboration

Communication skills

Problem solving

Education

Bachelor's degree in science or related field

Associate degree in science or related field

Tools

Excel

Electronic batch record (EBR) systems

CAPA software

Job description

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.

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

• Track and review manufacturing batch records and logbooks to ensure compliance with GDP and regulatory requirements
• Follow up with Manufacturing Technicians to ensure corrections are completed in a timely manner
• Ensure batch record review cycle time targets are consistently met

Error Tracking & Continuous Improvement

• Maintain error tracking metrics to identify, address, and correct repeated violations of GDP
• Review batch record structure and recommend simplifications to minimize errors, as applicable
• Coach shopfloor technicians on GDP principles and best practices

Quality & Compliance Escalation

• Identify and elevate GDP issues that could affect the safety, efficacy, and quality of drug substance
• Participate in deviation investigations and CAPA (Corrective and Preventive Action) creation, as applicable
• Support regulatory inspections and internal audits related to documentation practices

Team Collaboration

• Collaborate cross‑functionally with Manufacturing, Quality, and shopfloor teams
• Serve as a key point of contact for GDP‑related questions and guidance on the shopfloor

Physical Requirements

• Ability to work in a manufacturing environment, including cleanroom gowning requirements
• Regular walking and standing during shopfloor reviews and interactions with Manufacturing Technicians
• Occasional lifting up to 25 lbs
• Flexibility to respond to documentation or compliance issues outside of standard business hours, as needed

About You

Basic Qualifications

• High school diploma or equivalent.
• 1+ years of experience in a GMP regulated manufacturing environment.

Preferred Qualifications

• Associate or bachelor's degree in a science, engineering, or related field
• Prior experience in biopharmaceutical, pharmaceutical, or vaccine, biologics, or equivalent industries.
• Exposure to electronic batch record (EBR) systems
• Lean Manufacturing or continuous improvement training

Technical Skills

• Working knowledge of Good Documentation Practices (GDP) and cGMP regulations (21 CFR Parts 210, 211)
• Familiarity with batch record review and manufacturing logbook requirements
• Understanding of deviation investigation and CAPA processes, a plus
• Basic knowledge of error tracking and metrics reporting tools (e.g., Excel, electronic batch record systems), a plus.

Soft Skills

• Highly detail-oriented with the ability to work quickly and accurately
• Sound interpersonal and information‑gathering skills
• Ability to work effectively in a team environment and interact with others across all levels
• Strong written and verbal communication skills
• Proactive, quality‑focused mindset
• Demonstrated attention to detail and accuracy in documentation‑focused tasks
• Ability to work quickly and accurately under time constraints

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 Affimative 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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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.