Quality Systems Specialist

Job Summary

Supporting quality system activities remotely, the contract Quality Systems Specialist will maintain compliant quality processes, drive continuous improvement, and collaborate with cross-functional teams to foster a strong culture of quality.

Key responsibilities

• Support quality system activities related to deviations, CAPAs, change controls, investigations, and audit readiness
• Partner with global and site leadership teams to ensure adherence to Quality Management System principles
• Coordinate revisions to SOPs, forms, and templates for quality systems documentation

Required qualifications

• Bachelor's Degree in a scientific discipline
• 1-3 years of experience in the Pharmaceutical or Medical Device industry
• Experience working within effective cGMP quality systems, including SOP writing
• Familiarity with GMP requirements
• Ability to work autonomously in a fast-paced environment