Sanofi
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Qualification Engineer
role at
Sanofi
This range is provided by Sanofi. Your actual pay will be based on your skills and experience—talk with your recruiter to learn more.
Base pay range $74,250.00/yr – $123,750.00/yr
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
Part of the Site Quality Organization, 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.
Assigned areas include validation lifecycle activities such as Validation Planning, Biotech Process Validation, Equipment and Facility Qualification and Validation Risk Management.
Has signatory responsibilities for validation/qualification documents within assigned areas.
Has some knowledge in biotech manufacturing processes (i.e. viral antigen or formulation production).
Excellent communication skills and teamwork are a must, as will be working on cross functional project teams including members from Manufacturing Technology, Engineering and Regulatory Affairs.
Good interpersonal and influencing skills are important for a candidate’s success in this role.
About You Basic Qualifications
Bachelor’s degree is required. Bachelor’s degree in Engineering, Science or related field is preferred.
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.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Aff… (legal EEO statement continues in full).
Seniority level Mid-Senior level
Employment type Full-time
Job function Management and Manufacturing
Industries Pharmaceutical Manufacturing
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Qualification Engineer
role at
Sanofi
This range is provided by Sanofi. Your actual pay will be based on your skills and experience—talk with your recruiter to learn more.
Base pay range $74,250.00/yr – $123,750.00/yr
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
Part of the Site Quality Organization, 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.
Assigned areas include validation lifecycle activities such as Validation Planning, Biotech Process Validation, Equipment and Facility Qualification and Validation Risk Management.
Has signatory responsibilities for validation/qualification documents within assigned areas.
Has some knowledge in biotech manufacturing processes (i.e. viral antigen or formulation production).
Excellent communication skills and teamwork are a must, as will be working on cross functional project teams including members from Manufacturing Technology, Engineering and Regulatory Affairs.
Good interpersonal and influencing skills are important for a candidate’s success in this role.
About You Basic Qualifications
Bachelor’s degree is required. Bachelor’s degree in Engineering, Science or related field is preferred.
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.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Aff… (legal EEO statement continues in full).
Seniority level Mid-Senior level
Employment type Full-time
Job function Management and Manufacturing
Industries Pharmaceutical Manufacturing
#J-18808-Ljbffr