Job Offer: Sterility Insurance & Microbiology Expert, Sanofi
- (2025-04-04) – Sanofi is seeking a Sterility Assurance and Microbiology Global Expert to join its Quality Control Microbiology team in Framingham, Mass.The position offers a hybrid work arrangement,with...
- The expert will manage global expertise in sterility assurance and microbiology, including developing communities of practice.
- The Sterility Assurance & Microbiology team is responsible for developing policies to harmonize best practices, improve efficiency, and drive continuous enhancement across Sanofi.The team also analyzes and oversees...
Sanofi Seeks Global Sterility Assurance and Microbiology Expert in framingham,MA
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FRAMINGHAM,Mass. (2025-04-04) – Sanofi is seeking a Sterility Assurance and Microbiology Global Expert to join its Quality Control Microbiology team in Framingham, Mass.The position offers a hybrid work arrangement,with approximately 60% onsite work and 40% remote work,and involves about 25% travel.
Job Overview
The expert will manage global expertise in sterility assurance and microbiology, including developing communities of practice. The role involves providing strategic vision, technical expertise, and troubleshooting support to all Sanofi business units.
The Sterility Assurance & Microbiology team is responsible for developing policies to harmonize best practices, improve efficiency, and drive continuous enhancement across Sanofi.The team also analyzes and oversees initiatives to ensure current and future regulatory requirements are incorporated into the company’s quality system.
Key Responsibilities
- Provide leadership and guidance on technical aspects of drug and sterile manufacturing, including aseptic operations and contamination control.
- Develop and maintain Sanofi standards and supporting documents related to sterility assurance and microbiology.
- Lead experts from across Sanofi to assist with the assessment, development, and implementation of Sterility Assurance and Microbiology Programs.
- Provide input to projects for new facilities, equipment, and technologies.
- Support Sanofi sites in preparing for regulatory inspections.
- Support collaboration between digital, quality, and technical functions.
- Lead or participate in cross-functional teams to execute contamination control objectives.
- Interact with external bodies to broaden knowledge of industry practices and monitor regulatory developments.
Qualifications
Basic Qualifications
- Bachelor’s or Master’s degree in Microbiology, Biochemistry, Pharmaceutical sciences, or a related field; Microbiology is preferred.
- Minimum of 15 years of industrial experience in pharmaceutical/biotech sterile manufacturing.
- Strong quality mindset with experience in managing compliance and health authority regulations.
- Strong knowledge of contamination control strategy and quality risk management principles.
- Expertise in technical aspects of sterile manufacturing, including aseptic processes and environmental monitoring.
- Strong analytical and problem-solving abilities.
- Proven ability to lead cross-functional teams.
Why Sanofi?
Sanofi offers opportunities for career growth, a rewards package, and health and well-being benefits, including parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Chance and Affirmative Action employers committed to a culturally diverse workforce.
Compensation will be determined based on experience. Employees may be eligible for company benefits programs; additional details is available.
Sanofi’s Commitment
Progress is not done by itself, it is the people who build it: people from different backgrounds, in different places, in different roles, but all united by the same motivation: the will to make the impractical possible.
Sanofi
Sanofi states it believes in equal opportunities for everyone, irrespective of origin, skin color, beliefs, gender, sexual orientation, age, citizenship, civil status, disability or gender identity.
More information about diversity, equity, and inclusion initiatives is available on Sanofi’s website.
Sanofi’s Call for a Global Sterility Assurance and Microbiology Expert: Your Questions Answered
This article provides an in-depth look at Sanofi’s job opening for a Global sterility Assurance and Microbiology Expert. We’ll delve into the role’s responsibilities, qualifications, and what makes Sanofi a great place to work.
Q: What is Sanofi looking for in a Global Sterility assurance and microbiology Expert?
A: Sanofi is seeking a highly experienced professional to lead and manage global expertise in sterility assurance and microbiology. This role is based in Framingham, Massachusetts, and involves providing strategic vision, technical expertise, and troubleshooting support to all Sanofi business units.
Q: What are the primary responsibilities of this expert role?
A: The responsibilities are extensive but can be summarized as:
Providing leadership and guidance on technical aspects of drug and sterile manufacturing, including aseptic operations and contamination control.
Developing and maintaining sanofi standards and supporting documents related to sterility assurance and microbiology.
Leading experts from across Sanofi to assist with Sterility Assurance and Microbiology Programs.
Contributing input to projects involving new facilities, equipment, and technologies.
Supporting Sanofi sites in preparing for regulatory inspections.
Fostering collaboration between digital, quality, and technical functions.
Leading or participating in cross-functional teams focused on contamination control objectives.
Interacting with external bodies to expand industry knowledge and track regulatory developments.
Q: What qualifications are required for this position?
A: The ideal candidate will possess:
A Bachelor’s or Master’s degree in Microbiology, Biochemistry, Pharmaceutical sciences, or a related field (Microbiology preferred).
A minimum of 15 years of industrial experience in pharmaceutical/biotech sterile manufacturing.
A strong quality mindset and experience in managing compliance and health authority regulations.
Solid knowledge of contamination control strategy and quality risk management principles.
Expertise in technical aspects of sterile manufacturing, including aseptic processes and environmental monitoring.
strong analytical and problem-solving abilities.
* Proven ability to lead cross-functional teams.
Q: What type of work arrangement does this position offer?
A: The position is a hybrid role, involving approximately 60% onsite work and 40% remote work.
Q: Does the role involve travel?
A: Yes, the position involves approximately 25% travel.
Q: What does Sanofi offer to its employees?
A: Sanofi offers opportunities for career growth, a rewards package, and health and well-being benefits, including parental leave.
Q: What is Sanofi’s commitment to diversity and inclusion?
A: Sanofi is committed to equal opportunities for everyone, irrespective of origin, skin color, beliefs, gender, sexual orientation, age, citizenship, civil status, disability, or gender identity. Sanofi Inc. and its U.S. affiliates are Equal Chance and Affirmative Action employers committed to a culturally diverse workforce.
Q: Where can I find more details about Sanofi’s diversity and inclusion initiatives?
A: You can find more information on Sanofi’s website.
Q: What does Sanofi say about its vision for the future?
A: Sanofi’s commitment is clear: ”Progress is not done by itself,it is the people who build it: people from different backgrounds,in different places,in different roles,but all united by the same motivation: the will to make the impractical possible.”