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