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Employer Brightwater
Job Title QA Specialist

This is an opportunity to join an exciting and dynamic Pharmaceutical Company in Cork as a QA Specialist.

You will be responsible for carrying out tasks and projects related to managing compliance activities during qualification and validation.

On offer is a 12 month contract with a competitive hourly rate.

Job Duties and Responsibilities:

  • Ensure that compliance systems are implemented in an efficient manner.
  • Support the management of GMP compliance systems.
  • Review and/or approve non-conformance investigations.
  • Coordinate investigation activities to ensure root causes are identified and that corrective actions are taken.
  • Approves closure of non-conformance investigations on completion of the investigation and corrective actions.
Other Skills:

  • Work with other departments and functions to achieve and maintain a state of GMP compliance.
  • Establish effective partnerships with individuals and teams so that compliance activities are well understood and coordinated.
Qualifications and Experience:

  • Bachelors Degree in a scientific/technical discipline.
  • 2+ years experience in a quality, validation or compliance role within the biological and/or pharmaceutical industry.
For more information please call Simon on 021-4221000, or apply below.

This job originally appeared on
Location Cork
Date Added 129 days ago
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