
Manufacturing and Supply
Wo Wunder der Wissenschaft
für Patient*innen Realität werden
QC Expert - Microbiology
Auf einen Blick:
Unsere Teams produzieren und liefern jedes Jahr über 4 Milliarden Einheiten an Medikamenten und Impfstoffen und sorgen dafür, dass jede Innovation die Menschen erreicht, die sie am dringendsten benötigen. Unsere hochmodernen Produktionsstätten, KI-gestützten Smart Factories und wegweisenden Automatisierungstechnologien setzen neue Maßstäbe – damit Behandlungen Patient*innen schneller, sicherer und nachhaltiger als je zuvor erreichen. Hier kannst Du mit Deinen Fähigkeiten, Deinen Ambitionen und Deiner Leidenschaft die Zukunft des Gesundheitswesens mitgestalten.
Job Title: QC Expert - Microbiology
Location: Framingham, MA
Hours: Mon-Friday 830 a.m.-5:00 p.m.
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.
Quality Control Microbiology supports manufacturing activities at Sanofi’s Framingham Campus by detecting, quantifying and identifying possible contaminants that may interfere with the quality of the product during the difference 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 end product will meet the pre-defined standards for safety, purity, identity and effectiveness.
Quality Control Microbiology Scientist II develops and authors complex, explicit
documentation for new and current procedures, validation protocols and technical reports incorporating appropriate use of statistics. Solves assay/process problems. Identifies potential problems and proactively suggests technical solutions based upon analytical expertise and knowledge of product/process. Coordinates completion of specific project tasks with other departments. Provides contributions to the understanding and
interpretation of results and how they impact the design of subsequent experiments.
Contributes to development of project strategy in consultation with supervisor and/or colleagues. Train technicians and lower level analysts.
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?
Main Responsibilities:
Independently plans and executes projects in support of the QC Microbiology Laboratory.
Evaluates new technologies for implementation in the QC Microbiology Laboratory.
Uses in-depth technical knowledge to perform method validation.
Perform comprehensive data analysis, prepare statistical analysis of results and write technical reports.
Ensure GMP compliance of all activities performed.
Represent QC Micro in internal and external audits as required.
Oversee, plan and execute QC Micro qualification and re-qualification of lab equipment and campaigns supported by QC Microbiology (cGMP).
Ensure appropriate facility support and provide technical expertise.
Coordinate and support validation, engineering and production assignments according to schedule without compromising quality
Specify, procure, and coordinate validation and calibration and maintenance of laboratory equipment and instrumentation.
Review standard operating procedures; coordinate method development, alignment and validation as required.
Maintain positive relationship and network effectively across sites and organizations.
Provide in depth training and assist in the writing and development of training qualifications.
Mentors and direct the work of less experienced team members.
Provides project oversight and participate in cross-functional teams to maintain timelines established for QC Microbiology.
Perform assays and review as required.
Perform other additional job related duties as required.
Practice safe work habits and adhere to Sanofi’s safety procedures and guidelines.
About You
Basic Qualifications:
Bachelor’s degree in Life Sciences discipline and 5 years of experience in cGMP
lab environment, or Master’s degree in Life Sciences discipline and 3 years’
experience in cGMP lab environment.
PhD in Life Sciences discipline and 0-3 years’ experience in cGMP lab
environment.
Proficient in Microsoft Office and lab based data management systems.
Ability to present technical data.
Ability to work independently on scientific projects.
Familiarity with USP and global compendial regulations.
Scientific technical writing ability including authoring and revising SOPs, validation protocols and technical reports.
Experience troubleshooting of assay and equipment issues.
Working knowledge Aseptic practices and technique.
Preferred Qualifications
Proficient in Outlook and MS Word and Excel and lab based data management systems.
Special working conditions:
Must be able to lift 40 lbs.
Must be able to gown and gain entry to manufacturing areas.
Occasional nights, weekends and holidays may be require.
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 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.
#GD-SG
#LI-GZ
#LI-Onsite
#vhd
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.
Diversity und Inklusion sind in den Grundwerten von Sanofi verankert und spiegeln sich in unserer Arbeitsweise wider. Wir respektieren die Vielfalt unserer Belegschaft in Hinsicht auf ihre Herkunft, Erfahrungen und Lebensweisen. Wir erkennen die Bereicherung, die diese Vielfalt birgt, und fördern Inklusion sowie eine Arbeitsumgebung, in der diese Unterschiede sich weiter entwickeln können, zur Stärkung des Lebens unserer Mitarbeiter, Patienten und Kunden.
Mehr Informationen über diesen Standort

Warum bei uns arbeiten?
- Wir stellen nicht nur Medikamente her – wir bewirken etwas. Unser globales Netzwerk modernster Produktionsstätten sorgt dafür, dass Patient*innen die Behandlungen erhalten, die sie brauchen – genau zur richtigen Zeit.
- Innovation treibt uns an. Von KI-gestützter Fertigung bis hin zu weltweit führenden Produktionsmethoden setzen wir neue Maßstäbe in Effizienz und Leistung.
- Hier wachsen Karrieren. Ob in der Produktion, Qualitätssicherung, Ingenieurtechnik oder in der Supply Chain– arbeitest Du mit erstklassigen Talenten zusammen, entwickelst Deine Fähigkeiten weiter und gestaltest die Zukunft der Pharmaindustrie mit.
- Wir tun, was richtig ist. Sicherheit, Nachhaltigkeit, Vielfalt, Gleichberechtigung und Inklusion stehen im Mittelpunkt unseres Handelns – für ein Arbeitsumfeld, in dem alle erfolgreich sein können.
All-In für Vielfalt
Bei Sanofi führen unterschiedliche Perspektiven zu den besten Lösungen für Patient*innen. Erfahre von Monique Vessey, unserer Leiterin der Supply Chain -Transformation, wie ihre persönliche Geschichte ihre Arbeit bei der Bereitstellung lebenswichtiger Medikamente prägt.

"Manufacturing & Supply bildet die Brücke zwischen der Wissenschaft in unseren Forschungslaboren und den Menschen und Gemeinschaften, die wir versorgen."

Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
Mehr erfahren

Karriere in Manufacturing and Supply
Entdecke wie Sanofi die pharmazeutische Produktion und Supply Chain mit modernster Technologie, digitaler Innovation und nachhaltigen Prozessen transformiert. Ergreife Deine Chance, lebensverändernde Medikamente effizient und verantwortungsvoll bereitzustellen.

Biopharma-Innovation mit McLaren Racing beschleunigen
Was haben die Formel 1 und die biopharmazeutische Industrie gemeinsam? Geschwindigkeit, Präzision und das Streben nach Exzellenz. Erfahre wie Sanofi gemeinsam mit McLaren Racing die Medikamentenentwicklung mit modernster cutting-edge-Wissenschaft revolutioniert.

Mach mit bei unserer Talent Community
Was können wir gemeinsam erreichen? Unsere Teams arbeiten an Projekten, die Menschenleben nachhaltig verändern. Registriere Dich jetzt und erhalte die neuesten Stellenangebote, sobald diese veröffentlicht werden.