Quality Assurance Specialist Job Opportunity
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We are seeking a highly skilled Quality Assurance Specialist to join our team in Tipperary.
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This is an exciting opportunity for anyone who wants to be part of a successful and award-winning Pharmaceutical organization.
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* Complete auditing/review of batch documentation to ensure compliance to SOPs, GMPs and applicable regulations.
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* Review and approve production and analytical documentation accompanying the release of drug substance, drug product and packaged finished goods to ensure conformance to appropriate SOPs, GMP and regulatory requirements, including supporting QP certification.
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* Actively communicate and collaborate with functional areas to develop a strong working relationship and understanding of roles and responsibilities.
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* Utilise this network to help resolve comments and issues that arise during audit and review.
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* Manage product recalls and stock recoveries as appropriate.
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* Identify compliance gaps and make recommendations for continuous improvement.
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* Create and maintain assigned Standard Operating Procedures (SOPs).
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* Perform and review complaints and deviation investigations, change controls and Corrective Action Preventative Actions (CAPA's).
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* Assist in the induction process for new starters and training of other staff.
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* Generally follow standard procedures and consult with manager/supervisor to ensure resolution of exceptions.
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* Compile data for reports and presentations, provide data interpretation, draw conclusions.
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* Carry out all assignments to the standards of compliance, efficiency, innovation, accuracy and safety in accordance with Company and regulatory requirements.
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* Keep abreast of cGMP requirements as described in applicable worldwide regulations.
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* Represent the department on cross-functional teams.
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* Assist in the generation, review and approval of Technical & Quality Agreements.
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* Additional activities as assigned by the manager/supervisor
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