Quality Assurance Associate

Job Title: Quality Assurance Associate

Location: Andover, MA

Hours: Monday - Friday, typically 8am - 5pm (flex on times)

Type: Contract, Potential for extension or conversion to permanent

Responsibilities

• Review and approve various Good Manufacturing Practices {also cGMP} records (primarily batch records, formulation records).
• Ensure that all documents for batch release are reviewed for completeness and accuracy.
• Support the site relative to a constant state of inspection readiness.
• Recognize when an issue is beyond your sphere of influence and escalate immediately.
• May participate in the release of raw materials, as needed.

Requirements

• Bachelor's Degree

• Experience in pharmaceutical industry

• Mental agility to handle a large quantity and broad scope of different types of quality assurance work.
• Ability to work independently, problem solve and make recommendations for solutions.
• Role is primarily office-sitting. Position requires walking, sitting, standing, and carrying batch records from one location to another as Andover site is a campus setting

Benefits

System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.