Job Description

Job Description

Job title: Principal Investigator

Location: Swiftwater, PA

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.

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?​

This position is within the Quality Systems group and supports Formulation, Filling, Inspection and Packaging Manufacturing primarily through completion of deviation investigations. The candidate will work cross-functionally with Operations and various support groups to investigate root causes, implement effective corrective and preventative actions, and perform thorough product impact analyses.

Main Responsibilities:

• • Independently author and resolve deviations in order to meet production and product release requirements.

  • Communicating across multiple groups and levels to drive deviation closure.

  • Identifying interdepartmental process improvements and working cross-functionally to-implement them.

  • Utilizing root cause analysis techniques and technical impact analyses during the deviation investigation process.

  • Managing multiple priorities either independently or as part of a team in order to meet key deadlines and communicate issues and Progress across all levels of organization

  • Communicating (both written and verbal) progress and updates across multiple levels of the organization.

About You

Basic Qualifications:

• • A High School Diploma and 4+ years’ cGMP experience OR

  • An Associate’s Degree and 3+ years’ cGMP experience OR

  • A Bachelor’s degree

  • Ability to work extended and flexible hours (including weekends) when needed

  • Experience working within a production or quality department of a pharmaceutical/ manufacturing company

Preferred Qualifications:

• • Knowledge of continuous improvement techniques and problem-solving skills

  • Experience with authoring, writing and leading deviation investigations

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.​​

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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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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

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