QUALITY ASSURANCE ADMINISTRATOR

CREGG Recruitment is seeking a highly skilled Quality Assurance Administrator for a permanent role in Galway.
Our client, a leader in the pharmaceutical and medical device sector, is committed to delivering high-quality products while adhering to ISO 13485 standards. As a Quality Assurance Administrator, you will be responsible for critical quality activities, including particulate counting, equipment calibration, supplier qualification, and maintaining the Quality Management System (QMS).

QUALIFICATIONS & PROFESSIONAL SKILLS:

• Bachelor’s degree or diploma in Quality Assurance, Engineering, Life Sciences, or a related field.
• 1+ years’ experience in quality or a related discipline preferred.
• Strong attention to detail with excellent verbal and written communication skills.
• Understanding of customer quality and delivery requirements.
• Ability to impart knowledge clearly and concisely.
• Strong teamwork skills with a results-driven mindset.
• Strong decision-making and reporting abilities.

CONTACT INFORMATION:

For a confidential discussion or to find out more, please contact:
Brendan McMahon | Recruitment Consultant
Email: brendanmcmahon@cregg.ie
Phone: 086-1772-380
If you are looking for a challenging and rewarding career in Quality Assurance, Apply now!

• Perform routine particulate counting and environmental monitoring in controlled environments.
• Conduct calibration, maintenance, and equipment verification, ensuring all instruments function correctly and within specifications.
• Support the implementation and maintenance of the QMS to ensure compliance with ISO 13485 standards.
• Assist with supplier management activities, including supplier qualification, monitoring, and periodic revaluation to ensure compliance with regulatory and company standards.
• Review and maintain supplier documentation, such as certificates of analysis, quality agreements, and audit reports.
• Collaborate with suppliers to address quality issues and ensure timely implementation of corrective and preventive actions (CAPA).
• Assist in preparing and executing internal and external audits, ensuring accurate documentation.
• Document, investigate, and support the resolution of non-conformances, deviations, and complaints.
• Conduct sampling and testing of raw materials, in-process materials, and finished products.
• Maintain accurate records of quality-related data, test results, calibration activities, and supplier performance metrics.
• Assist in creating, reviewing, and revising quality documentation, including procedures, forms, and work instructions.
• Monitor and maintain cleanliness and compliance in controlled environments, adhering to established protocols.
• Participate in root cause analysis and support CAPA implementation.
• Ensure compliance with SOPs, regulatory requirements, and safety standards.
• Collaborate with cross-functional teams to address quality concerns and provide support during product inspections or testing.
• Provide input into identifying process improvements to enhance product quality and operational efficiency.