Description
An experienced Quality Assurance Specialist (QA Specialist) is needed to join a global biopharmaceutical organisation based in the hearty and cultural Irish capital.The project surrounds the organisation's new build facility requiring heavy knowledge of Upstream or Downstream processes.
As a Quality Assurance Specialist, you will be responsible for:
- Providing Quality and cGMP input and oversight for all start-up project activities through commercial readiness and ongoing product disposition.
- Provide QA support for risk-based verification activities in the capacity of Quality Assurance Subject Matter Expert.
- Review and approval equipment/utilities verification documentation from design to post-execution.
- Participate in verification quality risk assessments and provide quality oversight to ensure verification quality risk assessments are effectively maintained/controlled.
- Review and approval of functional area documentation (SOP, Work Instructions, Criticality Assessments, technical report and protocols).
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