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Quality Administrator

1 month ago

Galway, Galway, Ireland CREGG Full time

Direct message the job poster from CREGG

Technical Recruitment Consultant | Engineering, Life Sciences, Medical Devices and Manufacturing Recruiter | Human Resource Management & German…

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).

Roles and Responsibilities may include (but aren't limited to):

  • 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.

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

Phone: 086-1772-380

If you are looking for a challenging and rewarding career in Quality Assurance, Apply now

Seniority level

Associate

Employment type

Full-time

Job function

Quality Assurance, Manufacturing, and Production

Industries

Medical Equipment Manufacturing, Pharmaceutical Manufacturing, and Packaging and Containers Manufacturing

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