Job Opportunity
We are seeking a highly experienced and driven Qualified Person (QP) to join our organization in the Life Sciences industry.
This is a permanent full-time opportunity offering flexible working hours. As Qualified Person, you will be responsible for a range of activities within the Quality Release Department, including:
* Documentation review/control, deviation approval, material status assignment/disposition
* Product stability OOT/OOS data investigations, quality defect reports and quality data performance reporting
* Support for other Quality Systems activities relating to customer complaints, product recalls, Annual Product Quality Reviews, process change control and quality inspection systems
* Provide QP support for business units and laboratories
Nurture a continuously improving compliance culture within our organization and its clients. Manage personal client project assignments, including provision of Qualified Person support.
Requirements:
* BSc Degree or equivalent third level education
* Qualified Person Status in accordance with EC Directives
* Minimum 2 years experience in quality or production function within the pharmaceutical industry
A demonstrated self-starter with excellent interpersonal, decision-making, teamwork, and communication skills.
As a key member of our team, you will have the opportunity to contribute to the success of our organization and advance your career in the Life Sciences industry.