Sanofi
mRNA Quality Assurance Associate, Lot Release - Vaccines
This job is now closed
Job Description
- Req#: R2728335
Supporting the review and approval of master production records for the timely initiation of GMP manufacturing activities.
Supporting the review and approval of executed batch records and related documentation, resolves compliance issues and dispositions lots of drug substance, bulk drug product, drug product and clinical materials for use in clinical trials.
SME for quality review of manufacturing and quality control records to ensure compliance with specifications and regulations.
Helps ensure that all requirements, as stipulated in the appropriate QTA, have been met.
Issue/Review documentation, i.e. Deviations, CAPAs, OOS etc., as they occur.
Write and revise SOP, Forms, Work Instructions, other document types as needed.
Assist with internal and external audits.
Other duties as assigned.
Must have a Bachelor’s degree in a relevant field (scientific, manufacturing, quality, etc.) and preferably 3 years of experience in Quality Assurance.
Working knowledge and ability to apply Quality principles and cGMPs in conformance to standards, preferably gained from working in a manufacturing, QA or QC environment.
Demonstrated ability to interact and communicate effectively, both written and verbal, with peers, management, auditors, and consultants.
Must have excellent attention to detail, project and time management skills, and the ability to manage multiple priorities with aggressive timelines.
Preferred experience with outsourced manufacturing and testing operations.
Working knowledge of MS Office products including Word, Excel, Outlook, PowerPoint, and Microsoft Project.
In the race for the future of health– The Sanofi mRNA Center of Excellence (CoE)
At Sanofi, we believe in a world in which no one suffers or dies from vaccine-preventable diseases. And while the pandemic has shaken up our industry, creating new opportunities and risks, we believe the acceleration of innovation with mRNA technology means vaccines for more people faster than before.
That’s why we’re looking for bold, optimistic world-changers to join the team at our mRNA Center of Excellence. We’re investing €400m a year into the new Center, hiring a team of 400 dedicated employees for it and using it as the foundation to implement integrated end-to-end mRNA vaccine capabilities and research with R&D, digital and CMC teams.
Bring your ambition and optimism for the future to Sanofi. Join us!!
About the Opportunity
The Quality Assurance Associate reports to the Manager, Lot Release and is an integral part of the Quality team. This position offers opportunities to focus on disposition of product for Sanofi CoE, inclusive of review and release of manufacturing/test documentation from process development, manufacturing and nonclinical, clinical and commercial processes and supply chains. This includes batch records, deviations, CAPAs, CoAs, CoCs, etc.
This position is based in Waltham, MA. The ideal candidate will live within a reasonable daily commute time. This opportunity may require flexibility in working hours on occasion.
Key Responsibility:
The Quality Assurance Associate is responsible for:
Preferred/Desired Qualifications:
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.
#GD-SP
#LI-SPPDN
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
About the company
Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health.
Notice
Talentify is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Talentify provides reasonable accommodations to qualified applicants with disabilities, including disabled veterans. Request assistance at accessibility@talentify.io or 407-000-0000.
Federal law requires every new hire to complete Form I-9 and present proof of identity and U.S. work eligibility.
An Automated Employment Decision Tool (AEDT) will score your job-related skills and responses. Bias-audit & data-use details: www.talentify.io/bias-audit-report. NYC applicants may request an alternative process or accommodation at aedt@talentify.io or 407-000-0000.