What are the responsibilities and job description for the Quality Assurance Shop Floor Lead position at Sanofi?
Job title : Quality Assurance Shop Floor Lead
Location : Ridgefield, NJ
About the Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as Quality Assurance Shop Floor Lead within our Biosurgery Quality Team will be to ensure compliance with cGMP, regulatory, and internal requirements regarding the manufacturing, testing, and distributing of products through formal QA walkthroughs, Audits and Investigations that may result in additional training and recommendations to procedural improvements. Evaluate and provide QA recommendations for all products, systems, facilities, and issues that are affected or may be affected by regulatory or cGMP requirements.
Increase quality culture in the manufacturing areas. Enhance technical knowledge of operators and shop floor managers by providing positive and constructive feedback.
We are an innovative global healthcare company with one purpose : to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities :
- Conduct QA Shop Floor Walkthrough and Audit based on schedule and assignment (for both Sanofi locations)
- Documentation of appropriate findings and support area improvement
- Support the Manager to drive QA shop floor program and address concerns with manufacturing and driving quality improvements
- Mentoring and coaching QA Shopfloor personnel
- Coaching manufacturing team, when required
- Collaboration with manufacturing on process improvements
- Area / Line clearances, when requirerd
- Review documentation- BPRs, Logbooks
- Deviation support, when required
- Perform audits, walk-throughs, GEMBAs, technical coaching
- Support Manager with tasks as needed (Change Control, Deviations etc) /
- Support Additional Quality functions (Media Fill Observer, Documentation Updates etc)
- Author significant and non-significant deviations, change controls, report etc.
- Present department KPIs as needed
About You
Basic Qualifications / Requirements :
Preferred Qualifications :
Why Choose Us?
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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