QC Analyst Microbiology

SanofiFramingham, MA
$27 - $36Onsite

About The Position

The Quality Control team is dedicated to the development and validation of methodologies using state-of-the-art technology and responsible for ensuring that all production lots and materials meet the required quality standards, supporting regulatory compliance, and operational excellence of the organization. Sanofi is an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. They are also a company where employees can flourish and grow their careers, with countless opportunities to explore, make connections with people, and stretch the limits of what they thought was possible.

Requirements

  • High School Diploma or equivalent with a minimum of 4 Years of relevant industry experience.
  • Associate Degree or Bachelor’s Degree with 0-2 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.
  • Proficiency in Microsoft Office tools such as: Word, Excel & PowerPoint.
  • Experience with lab-based data management systems.
  • Experience in a Quality Control Laboratory.
  • Experience with Environmental Monitoring, including Water Testing.

Responsibilities

  • Executing analytical testing 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
  • Executing assigned CAPAs related to remediation plans, continuous improvements
  • Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately

Benefits

  • high-quality healthcare
  • prevention and wellness programs
  • at least 14 weeks’ gender-neutral parental leave
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