Sr. Research Associate- Scientific Performance Manager- Vaccines
Sanofi

Swiftwater, Pennsylvania

Posted in Manufacturing and Production


Job Info


Job title: Sr. Research Associate- Scientific Performance Manager- Vaccines

Location: Swiftwater, PA

About the Job

The Sr. Research Associate - Scientific Performance Manager will lead efforts with platform leads to ensure effective assay life cycle management (LCM) across all GCI scientific platforms. Key responsibilities include strategic planning for assay re-optimization and the implementation and management of performance monitoring and trending tools. The role also involves contributing to laboratory activities, clinical testing, and scientific data review and approval, as well as assisting with investigational studies, designing experiments, and developing new processes and test methods.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Main Responsibilities:

  • Ensure effective assay life cycle management (LCM) across all GCI scientific platforms including working with platform leads and SME's to plan and manage assay re-optimization, performance monitoring, and the implementation of trending tools.
  • Assist with investigational studies, experiment design, and the development of new processes and test methods.
  • Contribute to laboratory activities, clinical testing, and scientific data review and approval.
  • Promote and adhere to all quality and safety practices in compliance to all relevant regulatory, Sanofi/Sanofi Pasteur local and global procedures. Support a quality and compliant testing environment (laboratories, equipment, reagents, training and documentation, methods, personnel).
  • Document generation associated with project/objectives. This may include, but is not limited to, protocols, reports, operating procedures/instructions, regulatory correspondences, or presentations.
  • Support departmental quality by ensuring adequate support for documentation, investigation, and closure of quality items including change controls, deviations, and CAPAs.

About You

Education Requirements:
  • Specialized degree in biological sciences from an accredited University
  • Minimum of 2yrs at previous level +
  • B.Sc. + 3yr experience
  • M.Sc. + 1yr experience

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 and wellness programs and at least 14 weeks' gender-neutral parental leave.

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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