Quality Excellence Manager
Job in
Swiftwater, Monroe County, Pennsylvania, 18370, USA
Listed on 2026-10-26
Listing for:
Sanofi
Full Time
position Listed on 2026-10-26
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist, Data Analyst
Job Description & How to Apply Below
Quality Excellence Manager
Location:
Swiftwater, PAAbout the Job Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and 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 Promoting a culture of excellence and ensuring full implementation and sustainability of SMS 2.0
Identifying and implementing continuous improvement initiatives to enhance product quality and operational efficiency, in line with SMS 2.0 methodology
Monitoring and analyzing quality performance data to identify trends and areas for improvement
Supporting the investigational process of complex events to ensure the identification of the true root cause and relevant CAPADeveloping a culture of continuous improvement within the site Developing initiatives for staff and management team to foster the capacity to identify and implement quality improvements
Developing and maintaining quality metrics and performance indicators
Conducting regular assessments of quality processes and facilities
Implementing in quality department global quality initiatives related to operational excellence
Managing the quality excellence team and ensuring their proper qualification for their activities
Actively contributing to global networking and initiatives
Primarily on-site office-based with supportive presence on the manufacturing floor and ability to gown for Gembas.
Key Involvement In Decision Making Process Key Roles (D,A,I)
Decide on continuous improvement strategy and roadmap (D)
Advise on quality improvements and initiatives (A)
Advise on data-driven quality improvements (A)
Establish quality metrics in line with global quality (D)
Decide on initiatives to promote a culture of continuous improvement (D)
Advise on the development of quality performance metrics and reporting systems (A)
About You Basic Qualifications Bachelor's degree in science, Engineering, or a related technical field; master's degree preferred5+ years of experience in Quality Assurance roles, with a strong understanding of pharmaceutical manufacturing processes and regulatory requirements5+ years of experience in manufacturing or Operational Excellence, within the pharmaceutical, biotechnology, medical device, or another closely related regulated industry.
Technical Skills Ability to analyze complex data, identify trends, and make data-driven decisions to improve quality processes
Proficiency in Excel and Power BI to build dashboards and visualize insights
Leadership skills to guide cross-functional teams, manage projects, and drive quality initiatives
In-depth understanding of regulatory requirements and GMP in the pharmaceutical industry
Strong presentation skills, with the ability to communicate data-driven insights clearly to cross-functional teams and leadership
Soft Skills Strong communication and interpersonal skills, with the ability to influence without direct authority
Strong time management and prioritization in a fast-paced, cross-functional environment
Proactive, solution-oriented mindset, with the ability to anticipate risks and define clear action plans
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.
En…
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