Job Description
Quality Specialist RK21980 11 Months Dublin Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties: Provide direct Quality support to production and support areas. Provides presence on the shop floor to support compliance and data integrity. Review and approve GMP documentation/data for accuracy and completeness. Review and approve executed production documentation such as electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures and ensures completion of proper remediation of errors. QA support, review and approval of C&Q, Performance qualification (PQ) & Process Validation documents. Support sustaining activities such as change management, deviations, CAPAs, equipment requalification, periodic review, site maintenance & Calibration Programs. Provides support to internal audits and regulatory inspections. Collaborates with cross-functional team members in the identification and implementation of continuous improvement initiatives and action plans. Education and Experience : Bachelor degree, in a scientific or engineering field. 3 years of relevant post-degree experience in a GMP environment: manufacturing, laboratory, quality, operations, technical, or regulatory function. Technical writing skills. If interested in this posting please feel free to contact Rachel Kent on or for further information. Skills: GMP Quality Assurance Technical Writing