QA Specialist – III is required for a Cork based Biopharmaceutical company.
This role offers you a chance to work in a state of the art facility, in an innovative Biotechnology company, with excellent career development opportunities and a clear and committed patient focus.
The QA Specialist:
o Will be required to participate as site QA lead representative in the rollout of large and small projects in the QA systems group and across site such as changes to electronic document management and deviation management systems with associated QA review on all project change and validation documentation. May be requested to perform lead on some of these projects.
o Perform a wide variety of activities to ensure compliance with applicable regulatory requirements. These may include the running and design of weekly metrics for Training, On Time Deviations, On time CAPA closure and change controls along with other QA metrics.
o This role may be responsible for the weekly delivery of GMP Induction training and may be required to design and deliver annual GMP Refresher training. Also deliver one to one GMP training when business needs arises.
For this role you willl have :
o Some years of relevant experience in a GMP environment related field and a BS or BA.
OR Some years of relevant experience and a MS.
o Prior experience in pharmaceutical industry is preferred.
o Demonstrates proficiency in Good Manufacturing Practices (GMPs).
Call Regina in LSC on 0214777 329 to discuss this Senior QA Specialist role in more detail or apply directly via this advert