QA Specialist

Brightwater

Cork

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 RecruitIreland.com.

2375 days ago