Quality Control / Assurance

• Monitoring the production Environment
• Liaising with the Production Manager & Quality Department about any non-conformance issues.
• Inspecting incoming materials by confirming specifications and returning materials that do not meet standards.
• Carrying out Final Product Inspections on production line by ensuring the products conform to specifications.
• Implementing GDP standards in document inspection, completing reports and updating the database with all necessary information.
• Problem solving and continuous improvement investigations.
• To provide assistance and support to the Quality Engineering and Operations function.
• Drive continuous improvement 
• Training and overseeing all new staff on the production line.
• Ensuring GMP procedures and practices are upheld and implemented along with other quality standards.
• Carrying out other responsibilities as needed, based on the requirements of the department/role.

Qualifications and Education Requirements

• Leaving Certificate plus 3 years’ experience in a Medical Device assembly environment.
• Good IT skills are essential, previous cleanroom experience is also required.
• Understanding of GMP/GDP.
• An eye for detail.
• Ability to work on own initiative and with minimum supervision is required
• Good interpersonal skills and organisational skills.