Quality Excellence Manager
Job in
Reading, Berks County, Pennsylvania, 19601, USA
Listed on 2026-11-01
Listing for:
Sanofi Group
Full Time
position Listed on 2026-11-01
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
Swiftwater, PA:
Full time:
Posted Today:
End Date:
November 30, 2026 (30+ days left to apply):
R2872352
** Job Title**:
Quality Excellence Manager
*
* Location:
** Swiftwater, PA
** About 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 CAPA
* Developing 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 preferred
* 5+ years of experience in Quality Assurance roles, with a strong understanding of pharmaceutical manufacturing processes and regulatory requirements
* 5+ 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…
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