Quality Assurance Specialist - Pharma - Carlow, Ireland - 11-Month Contract
With worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a Quality Assurance Specialist to join their team to support multiple capital projects taking place onsite.
This is a fantastic opportunity to work on a state-of-the art fill-finish facility and the company’s first stand-alone vaccine and biologics plant outside the US.
Role Summary :
- Review and approval of all manufacturing batch documentation including electronic batch records, real time reports, master data using the site systems.
- Review and approval of SOP's, cleaning verification / validation data and other documents as necessary for the IPT department.
- Drive effective writing / revising / rolling out of accurate operational procedures, training materials and maintenance procedures for various Quality related systems; ensure all work is subsequently carried out in line with same.
- Support the development and implementation of improved quality reporting measures.
- Liaise with the Quality Specialists / QP / QA Lead to resolve queries relating to batch manufacturing process.
- Provide effective real time on the floor support for day-to-day manufacturing operations for example area clearances, batch record reviews, aseptic operations.
- Provide quality input into decision making process on the shopfloor ensuring that product quality is maintained.
- Provide training in all aspects of Quality Management Systems and GMP.
- Ensure all work is carried out in line with SOP’s, training, or other quality systems such as change controls where applicable.
- Facilitate compliance direction for the site by assisting in the adherence to divisional policies and guidelines as well as regulatory requirements.
Experience, Knowledge & Skills :
Relevant experience in a quality role, ideally in a pharmaceutical manufacturing environment.Knowledge of US and European cGMP guidelines, and other international regulatory requirements, as applicable to the site.GMP Audit experience in the pharmaceutical industryThird Level Degree qualified in a Science / Technical or related discipline.If this role is of interest to you, please apply now!
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