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USA - Quality Inspector I (Manufacturing/Quality) 1st Shift (contract)

Sanofi
Framingham, MA Contractor
POSTED ON 3/20/2025 CLOSED ON 4/20/2025

What are the responsibilities and job description for the USA - Quality Inspector I (Manufacturing/Quality) 1st Shift (contract) position at Sanofi?

Job Summary

Join Sanofi's contingent workforce program, FLEXT Direct, as a Manufacturing Technician I for a 12-month contract. In this role, you will be responsible for operating general manufacturing equipment in the production of Flublok Drug Substance within a cGMP commercial manufacturing facility. Your primary duties will include operating, maintaining, and cleaning large-scale cell culture bioreactors, executing techniques for cell expansion, and ensuring adherence to safety guidelines and quality standards.

Responsibilities

  • Demonstrate an in-depth understanding of techniques and processes involved in daily operations.
  • Conduct large-scale bioreactor cell expansion and protein production activities including equipment preparation and material sampling.
  • Perform cell analysis, data interpretation, and contamination checks using specialized equipment.
  • Operate and maintain ancillary equipment such as floor scales, turbidity meters, tube welders, and peristaltic pumps.
  • Collaborate with other departments to address manufacturing quality issues.
  • Manage and analyze manufacturing data while identifying issues and proposing solutions.
  • Ensure compliance with cGMP training requirements and participate in facility cleaning according to SOPs.
  • Work flexible schedules including weekends and holidays as needed by the department.


Skills

  • High School degree with at least 2 years of experience or training in a cGMP manufacturing environment.
  • Knowledge of cGMP, GDP, and SOPs.
  • Fluent in English with strong communication skills.
  • Basic understanding of Baculovirus Expression Vector System (BEVS) process is desired.


Qualifications

  • High School degree or equivalent
  • Minimum 2 years of experience or training in a cGMP manufacturing environment
  • Proficiency in English language
  • Strong communication skills


This position offers an exciting opportunity to work within a cutting-edge pharmaceutical manufacturing environment where you can contribute to the production of life-saving medications. If you are looking for a challenging role that allows you to showcase your technical skills while adhering to strict quality standards, this position is ideal for you. Join our team today!

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