We are seeking a Quality Systems Specialist to join our global pharmaceutical company on a permanent basis, with the option for hybrid work.
Key Responsibilities and Reporting Lines
The successful candidate will be responsible for supporting the management of electronic Quality Management Systems (eQMS) related processes, including:
* Documentation management
* Change controls
* Deviation management
* CAPAs
* Customer complaints and Laboratory Investigations
They will also lead and execute development and/or modification of the company's eQMS, as well as develop and approve written procedures and other documents required in support of eQMS.
Key Deliverables
The successful candidate will be responsible for developing and maintaining dashboard reports, providing accurate, complete, and consistent data across all quality systems. They will also participate in the preparation and delivery of associated training on site.
Position Requirements
To be successful in this role, you will need:
* 3+ years' experience in the Pharmaceutical Industry and a 3rd level qualification in a scientific discipline
* Strong communication skills and interpersonal skills
* Strong IT skills
* Strong writing skills
* Strong attention to detail
About Us
We are a leading Irish provider of specialist Scientific Recruitment, part of the CPL Group.