A leading global healthcare manufacturer is seeking a CAPA Specialist to join its team. This is an excellent opportunity for a quality assurance professional with strong experience in quality records and CAPA systems.
The CAPA Specialist will be responsible for:
* Leading weekly CAPA meetings to monitor timelines, quality, and progress of quality records and related actions.
* Providing leadership and support to all plant personnel in the effective use of the corrective and preventive action (CAPA) system.
* Monitoring and reporting monthly metrics related to CAPAs and quality records.
* Ensuring site quality CAPA metrics are accurately recorded, verified, and aligned with corporate expectations.
* Delivering training to subject matter experts and broader plant teams on CAPA processes, in line with site, division, and corporate standards.
* Reviewing site quality records to ensure compliance with rubric requirements, as well as site and divisional policies.
The ideal candidate will have:
* A diploma or degree in science, engineering, or a related discipline.
* At least 3 years' experience in a quality assurance role within a regulated manufacturing environment.
* Strong interpersonal and communication skills, with the ability to influence and engage across teams.
* A high level of computer literacy.
* Proven ability to contribute effectively within a high-performance team environment.