Senior QA Associate

9 hours ago

Dublin, Ireland PE Global Full time

Description: PE Global is currently recruiting for a Senior QA Associate on behalf of a leading biotech company based in Dublin South. This is an initial 12-month contract and a shift role Overview: The Plant Quality Assurance (PQA) Snr Associate will report to the QA Manager and will be a core member of the site Quality Assurance team. The PQA Snr Associate will serve as Quality point of contact for manufacturing operations. The site is focused on continuous improvement of all work processes and practices, therefore in addition to routine Quality Assurance duties, PQA Snr Associates may be asked to carry out additional work functions to support site continuous improvement activities. This is a 24/7 shift role required to support manufacturing operations. Key Responsibilities: Perform all activities in compliance with safety standards and SOPs. Write, review and approve Standard Operating Procedures in accordance with Policies. Provide Quality support for triage and investigation of all classes of non-conformance (NC) events. Review and approval of deviations for closure ensuring compliance with appropriate documentation. Participates in customer complaint investigations. Provides training and advice to staff in order for them to perform their desired functions. Observe and provide real-time quality oversight, and support for production unit operations, extending to formulation, vial and Syringe Fill Finish related activities, including observation and provision of direction during media fills and assessment of aseptic interventions. Review/approve production batch records, and associated documentation in preparation for Qualified Person disposition activities. Review and approve cGMP records ensuring compliance with appropriate documentation. Support continuous improvement and Operational Excellence initiatives. Education and Experience: University degree. Engineering or Science related discipline preferred. Relevant experience (4 yrs +) working in the pharmaceutical or biotechnology industry or other combination of experience and educational background that may otherwise satisfy the requirements of the role. Excellent written and verbal communication skills. Experience working with dynamic cross-functional teams and proven abilities in decision making. Strong organizational skills, including ability to follow assignments through to completion. Demonstrated ability in problem solving and experience in managing Root Cause Analysis /Deviation investigations. Experience working in aseptic operations, protein formulation, vial and syringe filling. Knowledge of applicable Regulatory requirements, and ability to evaluate compliance issues. Interested candidates should submit an updated CV. Please click the link below to apply, call Kellie on or alternatively send an up to date CV to ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland*** Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert. Skills: quality assurance fill finish GMP

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