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QA Associate

Job description

QA Associate

Our leading pharmaceutical client is seeking a QA Associate to joing their team in Cork. This is an 11-month contract. 

Job responsibilities:

  • Ensure site preparation for GMP operations by supporting cross functional initiatives
  • Review and approve electronic and paper production batch records
  • Release Raw Materials for production
  • Support Technology Transfer of a new product into the site including raw material and supplier qualification
  • Review and approve Trackwise deviation and investigations reports, ensuring root causes have been identified and corrective action implemented
  • Provide support as required: Document control, New or updates to relevant quality agreements, process and Cleaning Validation activates

The successful candidate will have:

  • Bsc of Science degree, or equivalent, in a technical discipline (physical, engineering, chemical or biological science, pharmacy)
  • Minimum 3 years relevant experience in a cGMP regulated manufacturing environment, with exhibited knowledge and proficiency in Quality Assurance and Compliance
  • Experience in supporting manufacturing operations, batch record review and deviation/CAPA is highly desirable

 

If you would like to discuss this role, reach out to Louise Whitty on 021 2359140 / lwhity@sigmar.ie  

 

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