Quality Assurance Professional for Pharmaceutical Manufacturing

6 days ago


Lexington, Kentucky, United States GQR Full time
About the Role

We are seeking a skilled Quality Assurance Associate to join our team in Lexington, MA.

This is a 6-12 month contract position offering an hourly rate of $55.00.

Responsibilities
  • Support clinical phase manufacturing by maintaining quality presence at GMP facility.
  • Conduct batch record review and resolve quality issues.
  • Assist with incoming raw material release and document management.
  • Provide training and ensure compliance with regulations and internal procedures.
Requirements
  • Minimum BA/BS in science related field.
  • At least 5 years experience in pharmaceutical, biotech, or medical industry.
  • Knowledge of Good Manufacturing Practices (GMPs) and Good Documentation Practices.


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