QC Analyst

Sanofi • Framingham, MA

23h • $32 - $43 • Onsite

About The Position

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, fast 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.

Requirements

• High School Diploma with a minimum of 6+ Years of relevant industry experience.
• Associate Degree with 4+ Years of relevant industry experience.
• Bachelor’s Degree with 2+ Years of relevant industry experience.
• Master's Degree with 1+ Years of relevant industry experience
• Proficient with Microsoft Office tools such as Word, Excel & PowerPoint.

Nice To Haves

• 1 Year of Experience in a GMP lab environment.
• Experience with lab-based data management systems.
• Experience in a Quality Control Laboratory.

Responsibilities

• Collect Environmental Monitoring (Viable Air, Viable Surface, Non-Viable Air Samples) and Critical Utility (RO, DI, WFI, Steam Water Samples, and Compressed Air and Mixed Gases Samples) in a timely manner, ensuring adherence to the committed scheduled plans
• Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks
• Recording all expected raw data, calculations, information related to his/her tasks, to comply with cGMP and data integrity requirements
• Ensuring that he/she is trained and qualified to the assigned analytical testing that requires to be qualified
• Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans
• Informing his/her manager of any quality or HSE event (deviations, OOS,) in a timely manner to ensure investigation and impact assessment are performed appropriately
• Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately
• Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately
• Ability to perform tasks in a Quality Control Laboratory environment and capable of lifting at least 10 pounds.
• May be required to pass vision exam to perform specific responsibilities.
• May be required to enter into controlled environments following proper gowning protocols

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED