QA Release

Sanofi; Swiftwater (Monroe County); On-site; USD 69,000 - 100,000; Full time

Job summary

Sanofi in Swiftwater, PA is seeking a QA Release specialist to manage batch review and release activities ensuring compliance with cGMP, FDA regulations, and site procedures.

You will perform final quality reviews of batch records, support batch disposition, and prepare Lot Release Protocols, ESUMs, and working documents, while collaborating with a cross-functional QA team to meet release timelines.

Qualifications

• Bachelor's degree and 1+ years in GMP pharmaceutical environment.
• Meticulous batch record review and documentation.
• Strong attention to quality, compliance, and regulatory standards.

Responsibilities

• Quality review of batch records for completeness and accuracy.
• Disposition of batches after verification of testing results.
• Prepare and review Lot Release Protocols (LRP) for regulatory submission.
• Prepare ESUM summaries and ensure release timelines are met.
• Prepare and certify working documents and provide QA metrics.

Skills

Batch record review

GMP experience

Data analysis

Quality Assurance

Microsoft Excel

Communication skills

Education

Bachelor's degree

Tools

SAP

FaCT

Job description

Job Title: QA Release Location: Swiftwater, PA

About the job: Your job, as QA Batch review specialist within our Quality Assurance team, will be to ensure product quality through batch release processes to market for the Swiftwater Site. This role will operate under flexibility to perform the necessary activities to ensure compliance requirements and manufacturing/release schedules are met. This role supports core activities: Preparation & Certification of Working Documents, Quality Review of Batch Records from Swiftwater and CMOs, Batch Disposition from Swiftwater and CMOs, Quality Review of Lot Release Protocols, Compliance and Performance.

Benefits of working in this role:

Be part of an inspiring mission to create life‑saving vaccines Leading a skilled and motivated team of quality professionals The work environment is a highly collaborative and technical vaccine manufacturing operation on a beautiful park like campus. 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

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 andwellness 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.

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. 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 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.