Contamination Control Specialist

Job Title: Contamination Control Specialist

Location: Framingham, MA

About The Job:

The Sterility Assurance and Microbiology (Contamination Control) Department supports quality and manufacturing activities at Sanofi Framingham Biologics Campus by identifying possible trends from microbial contaminants that may interfere with the quality of the product during different stages of the manufacturing process. It aims to maintain a state of microbiological control in the Utility Systems and within the environment where the manufacturing process is executed. It assesses the aseptic behavior of the personnel involved in these processes; and contributes to the guarantee that the areas are operating in a state of environmental control.

Join a global network that powers how Sanofi delivers, seamlessly, purposefully, and at scale. In Manufacturing & Supply, you'll help reimagine how life-changing treatments reach people everywhere, faster.

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main Responsibilities:

Leading as SME specific subjects part of the Contamination Control SOP in her/his area of expertise

Conducting risk assessments related to contamination control

Overseeing sites activities and performance for contamination control systems in her/his scope of responsibilities

Leading investigation following contamination control failures and proposing corrective and preventive actions (CAPA)

Collaborating with cross-functional teams to ensure product quality

Ensuring presence on the shop floor to oversee practices, identify gaps vs SOP for contamination control

Reviewing data from contamination control monitoring to propose improvements as necessary (from monitoring and trends)

Participating in audits and regulatory inspections and audits, providing expertise on contamination control

Supporting the preparation of validation protocol and supporting projects related to her/his area of expertise

Contributing as an SME to specific CoE/CoP with Global functions; implementing on site the best practices shared

 

Key Roles

Advise on contamination control protocols and procedures

Propose corrective and preventive actions to improve contamination controls

Advise cross-functional teams on best practices or expected improvements in her/his area of expertise

Presence on the shopfloor with formal traceability of the observations. Inform management and feedback operators

Contribute to quality documentation SOP and validation protocol

Additional Accountabilities

Experience in sterility assurance and microbiological or contamination control within a pharmaceutical or biotechnology environment

Ability to meticulously review and analyze documentation, processes, and products to ensure compliance with Sanofi GOP / Quality standards

In-depth knowledge of regulatory requirements and Good Manufacturing Practices (GMP) relevant to sterility assurance and microbiological control

Communication skills to communicate with a large number of functions (from shopfloor to management) and to present complex subjects

Ability to organize and lead routine investigations with a multi-disciplinary team

About You:

Basic Qualifications

Bachelor's degree in Life Sciences, Sciences, Engineering or other related fields with 8+ years experience working in a regulated, cGXP environment OR

Master's degree in Life Sciences, Sciences, Engineering or other related fields with 6+ years of experience working in a regulated, cGXP environment.

Preferred Qualifications

Operations experience in one or more of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation is preferred.

Clear understanding of cGMP via experience in working in a regulated environment

Demonstrated knowledge of cGXP regulations and guidance.

Demonstrated experience with change control, CAPA and deviation quality systems.

Demonstrated experience with project management

Skills:

Experience with Trackwise or equivalent system

Experience with metrics and trending

Experience with analytical instrumentation

Experience with Environmental Monitoring and Critical Utilities

Ability to work independently with minimal supervision and direction

Ability to function well in a fast paced environment

High attention to detail and accuracy

Self-motivated and highly organized

Experience with project management

Hands on problem solving and strong analytical skills

Strong computer skills

Special Working Conditions

Ability to gown and gain entry to manufacturing and Quality Control areas.

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.

Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.

Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale.

Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

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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Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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.

North America Applicants Only

The salary range for this position is:

$113.250,00 - $163.583,33

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.