Main Responsibilities
Quality Review of Batch Records
Perform final Quality review of completed manufacturing records for completeness and accuracy according to site procedures, cGMP, FDA’s 21 CFR, and other applicable health authority regulations.
Complete all required system transactions associated with the batch record review process.
Provide data for PDR manufacturing dates and Commodity Verification Sheets to allow further processing of material.
Disposition of Batches
Review Specification Checklist, Certificate of Analysis (and Conformance) to verify all required testing has been performed and all testing meets requirements prior to batch disposition.
Verify CBER release is received (if applicable) prior to batch disposition.
Verify the lot is not on hold (i.e., deviations, change controls, Approve for Further Manufacture database, etc.) prior to batch disposition.
Verify all previous manufacturing steps, including raw materials, are satisfactory prior to final disposition of the batch.
Complete all required system transactions associated with the batch disposition process.
Act as delegate to the QA Release Lead to provide approval to ship to external manufacturers, as assigned
Quality Preparation and Review of Lot Release Protocol (LRP)
Prepare and Review working LRP for completeness and accuracy prior to submission to the applicable Health Authority.
For licensed international products- ensure the batch is in full compliance with the GMP requirements and the specifications in the Marketing Authorization of the importing country.
Ensure LRP review meets cycle time requirements for product releases and SAP confirmation for completion of activity.
Preparation of Environmental Monitoring Summary (ESUM)
Oversee the ESUM process to ensure timelines and compliance standards are met.
Take assigned lots and complete ESUM reports by compiling and reviewing data in compliance with area EM procedures, finalizing ESUMS in the electronic ESUM database, and meeting release timelines.
Serve as the SME and function as a liaison for any assigned focus factory initiatives and participate on teams, communicating issues and identifying solutions to support release timelines.
Contribute to team objectives and priorities on assigned projects.
Preparation & Certification of Working Documents
Prepare batch records from master documents in the electronic document management system according to procedure
Ensure right first time preparation and completion of required documentation via electronic system (SAP and/or FaCT)
Provide support as required to ensure records are prepared and certified in accordance to the production planning schedule.
Certified prepared batch records to ensure completeness and accuracy in accordance to procedure.
Provide metrics in support of +QDCI board meetings.
Compliance and Performance
Meet department safety, quality, productivity, and cost targets and goals in a compliant and timely manner Act as Trainer for Batch Release activities.
Investigate deviations, as assigned.
Perform special projects as assigned by FFIP QA Leadership team.
Continuously reviews PQBR processes, and recommends, develops and implements efficiency and quality enhancements.
Perform CAPA review and approval as required
Completion of additional tasks as assigned by team Lead
Key Involvement in Decision Making
Prioritize quality and compliance objectives (D)
Approve a batch record if it is correctly completed and meets the quality requirement for one lot (D)
Check whether all practices are done according to quality requirement; if not, assure that a deviation is opened and reported in the batch record (D)
Review documentation for batch disposition (A)
Advise on initiatives to promote a quality-focused culture (A)
Advise on how to present a topic and answer specific questions (A)
About You
Basic Qualifications
Bachelor's degree.
1+ years of experience in a GMP-controlled pharmaceutical environment (e.g., Quality Assurance, Production, Quality Control or related areas).
Technical Skills
Ability to meticulously review batch records and documentation to ensure accuracy and compliance with regulatory standards.
Capability to investigate and resolve issues or deviations related to batch release processes efficiently.
Ability to manage multiple projects simultaneously, ensuring timely completion and adherence to quality standards.
Strong Computer Literacy (including Microsoft excel, power point, word)
Soft Skills
Ability to analyze complex data and identify trends, issues, and solutions
High level of accuracy and attention to detail in all quality assurance activities
Proficiency in identifying problems and implementing effective corrective actions
Strong verbal and written communication skills for effective interaction with team members and regulatory bodies
High level of autonomy
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; 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.
#GD-SP
#LI-SP
#VHD
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
$69.000,00 - $99.666,66
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.
