Quality Systems Engineer - QMS Focus

Your responsibilities

Act as Corrective Action/Preventive Action (CAPA) administrator by facilitating the (CAPA) system. This includes initiating CAPA’s, overseeing timelines, managing the CAPA log, reporting CAPA related metrics and leading CAPA review board meetings to ensure compliance.

Manage external audit activities including certification (notified body) audits and customer (contract manufacturing) audits. This consists of taking an active role in the audit process, as well as acting as liaison with external parties, scheduling audits, organizing and facilitating resources, communicating audit responses, maintaining the audit schedule and reporting all audit related metrics.

Facilitate all internal audit activities. This includes planning, assigning resources, managing the internal audit schedule, and reporting audit related metrics.

Gather and manage KPI/metric data used to measure the QMS.

Assist quality management representative (QMR) in conducting annual quality management reviews per ISO 13485:2016.

Create and/or update procedures and work instructions to capture improvements to quality management system process’.

Assist subject matter experts in the development, authoring and releasing of procedures and work instructions used to define their processes.

Understand, utilize and assist in maintaining document controls and change controls within the QMS.

Ensure processes and documentation comply with quality system regulations.

Your qualifications

BS in Engineering or related field preferred, or equivalent in experience and training

Working knowledge of the medical device regulated industry, to include ISO 13485 and FDA 21CFR820 regulations

Basic knowledge of statistical and engineering principals

Strong analytical and problem solving skills

Strong proficiency in root cause analysis to include tools and methodology

Proficient in Microsoft Office applications