Corrective and Preventive Action (CAPA) Facilitator

Job overview

The Corrective and Preventive Action (CAPA) Facilitator role is onsite in Reedsville, Pennsylvania. Compensation is not specified. The role supports quality systems and audit readiness. The facilitator manages CAPA activities from initiation through closure, coordinating investigations, implementation, and effectiveness verification. By monitoring timelines and documentation and supporting audit readiness, the role helps maintain compliance with FDA and ISO quality-system requirements.

What you'll do

• Manage the CAPA lifecycle from initiation to closure
• monitor timelines, aging, and effectiveness
• facilitate review meetings and follow-ups
• review CAPA documentation for compliance
• support audit and inspection readiness activities.

What we're looking for

Skills & competencies

capa facilitator

corrective and preventive action

quality systems

capa lifecycle

root cause analysis

nonconformance management

eqms

quality metrics

fda compliance

iso 13485

reedsville pa

katalyst healthcares & life sciences

Work arrangement

• Weekend coverage required

Why this role

Preferred qualifications include a bachelor’s degree in engineering or life sciences, eight years of medical-device quality-systems experience, at least three years of CAPA management, and experience supporting regulatory audits and inspections. Required skills include root-cause analysis, nonconformance and deviation management, eQMS, and quality metrics reporting.

About the employer

Katalyst Healthcares & Life Sciences is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.