What are the responsibilities and job description for the USA - Manufacturing Associate I (Manufacturing/Quali (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 play a crucial part in the production of Flublok Drug Substance within a large-scale recombinant protein production facility. Your responsibilities will include operating general manufacturing equipment, maintaining quality standards, ensuring safety compliance, and executing various tasks related to cell culture bioreactors and associated operations.
Responsibilities
Join Sanofi's contingent workforce program, FLEXT Direct, as a Manufacturing Technician I for a 12-month contract. In this role, you will play a crucial part in the production of Flublok Drug Substance within a large-scale recombinant protein production facility. Your responsibilities will include operating general manufacturing equipment, maintaining quality standards, ensuring safety compliance, and executing various tasks related to cell culture bioreactors and associated operations.
Responsibilities
- Demonstrate expertise in executing routine techniques and processes.
- Conduct large-scale bioreactor cell expansion and protein production activities.
- Perform cell analysis, data interpretation, and microscope operation for contamination checks.
- Operate and maintain ancillary equipment such as turbidity meters, tube welders, peristaltic pumps, etc.
- Collaborate with other departments to resolve manufacturing quality issues.
- Manage and analyze manufacturing data effectively.
- Identify issues, propose solutions, troubleshoot problems with minimal supervision.
- Ensure compliance with cGMP training requirements and SOPs.
- Participate in facility cleaning following sanitary maintenance SOPs.
- Adhere to established procedures for material flow within the facility.
- High School diploma with at least 2 years of experience in a cGMP manufacturing environment.
- Proficiency in cGMP principles, GDP, and SOPs.
- Fluent in English with excellent communication skills.
- Basic understanding of Baculovirus Expression Vector System (BEVS) manufacturing process is a plus.
- High School degree or equivalent
- At least 2 years of work experience or training in a cGMP manufacturing environment
- General knowledge of cGMP, GDP, SOP’s
- Fluent in English (written and spoken)
- Good communication and social skills
