I am currently seeking a quality compliance specialist for a sought-after Pharmaceutical company based in Waterford.
As their team grows, you will be responsible for quality compliance activities related to quality investigations, change management, supplier change, documentation lifecycle, and compliance reporting. This role offers flexible and hybrid working.
The successful candidate will have a related degree in science or engineering coupled with 3 years' experience in a similar role. Ideally, you will have previous experience in QC or Micro. You will have knowledge and experience of cGMP and GDP with exposure to quality systems in a regulated environment.
Responsibilities include:
* Perform and manage CAPA, Change Control, Investigations, periodic documentation lifecycle requirements, and report generation.
* Participate in the review of Quality Metrics for Quality Control.
* Actively contribute to Quality Control procedure effectiveness, simplification, and continuous improvement.
* Ensure effective coordination and support for external and internal audits.
* Perform critical/constructive review of procedures and practices.
* Identify and lead projects to make change improvements.
* Consult with Quality Assurance Representative to support and improve RFT and audit readiness.
If this role is of interest, please 'apply now' or contact me on 021 2300 300.
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