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

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 operate general manufacturing equipment in the downstream processing and buffer preparation areas of a cGMP commercial manufacturing facility. Your primary responsibilities will include executing techniques such as centrifugation, filtration, chromatography, and clean-in-place procedures while maintaining high-quality standards and adhering to safety guidelines.

Responsibilities

• Demonstrate an in-depth understanding of routine techniques and processes.
• Operate and maintain downstream processing equipment and ancillary tools.
• Collaborate with other departments to address manufacturing quality issues.
• Manage and analyze manufacturing data effectively.
• Identify issues, propose solutions, and communicate with management.
• Ensure compliance with documentation practices and cGMP training requirements.
• Participate in facility cleaning and follow SOPs for material flow.
• Work flexible hours including weekends and holidays as needed.
  
  
  

Skills

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

Qualifications

• High School degree or equivalent.
  
  
  

This is an exciting opportunity to be part of a dynamic team in a cutting-edge manufacturing environment. If you are looking to contribute your skills to the production of life-saving drugs while gaining valuable experience in the pharmaceutical industry, this role is perfect for you. Join us in making a difference in global healthcare.