Sanofi US
Job Title
Qualification Engineer 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. This position is responsible for providing Quality & Compliance oversight to site validation projects related to Drug Substance and/or Drug Product Vaccine manufacturing. Main Responsibilities
The individual would be part of the Site Quality Organization and will participate in project teams involved in site biotech facilities, processes and equipment for the manufacture of Drug Substance and/or Drug Product Vaccines and will review and approve validation related studies for assigned areas. These assigned areas would include validation lifecycle activities such as Validation Planning, Biotech Process Validation, Equipment and Facility Qualification and Validation Risk Management. This position has signatory responsibilities for validation/qualification documents within assigned areas. Candidates should have some knowledge in biotech manufacturing processes (i.e. viral antigen or formulation production). Excellent communication skills and teamwork are a must, as individual will be working on cross functional project teams which include members from various organizations within Sanofi Pasteur such as Manufacturing Technology, Engineering and Regulatory Affairs. Good interpersonal and influencing skills are important for a candidate’s success in this role. About You
Bachelor’s degree is preferred, and a Bachelor’s degree in Engineering, Science, or related field is required. 5+ years’ experience preferably in a cGMP environment. 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. Compensation
The salary range for this position is $74,250.00 - $123,750.00. All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in company employee benefit programs. Equal Opportunity
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Aff... (succinct EEO statement retained). All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, age, ancestry, disability, veteran status or any other characteristic protected by law.
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Qualification Engineer 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. This position is responsible for providing Quality & Compliance oversight to site validation projects related to Drug Substance and/or Drug Product Vaccine manufacturing. Main Responsibilities
The individual would be part of the Site Quality Organization and will participate in project teams involved in site biotech facilities, processes and equipment for the manufacture of Drug Substance and/or Drug Product Vaccines and will review and approve validation related studies for assigned areas. These assigned areas would include validation lifecycle activities such as Validation Planning, Biotech Process Validation, Equipment and Facility Qualification and Validation Risk Management. This position has signatory responsibilities for validation/qualification documents within assigned areas. Candidates should have some knowledge in biotech manufacturing processes (i.e. viral antigen or formulation production). Excellent communication skills and teamwork are a must, as individual will be working on cross functional project teams which include members from various organizations within Sanofi Pasteur such as Manufacturing Technology, Engineering and Regulatory Affairs. Good interpersonal and influencing skills are important for a candidate’s success in this role. About You
Bachelor’s degree is preferred, and a Bachelor’s degree in Engineering, Science, or related field is required. 5+ years’ experience preferably in a cGMP environment. 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. Compensation
The salary range for this position is $74,250.00 - $123,750.00. All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in company employee benefit programs. Equal Opportunity
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Aff... (succinct EEO statement retained). All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, age, ancestry, disability, veteran status or any other characteristic protected by law.
#J-18808-Ljbffr