Job Description
A Quality Assurance Specialist will be responsible for the daily production operations of a Pharmaceutical Client in Sligo.
Duties:
* Carry out in-process quality testing methods.
* Ensure all manufacturing documentation is completed accurately and on time, adhering to cGMP guidelines.
* Maintain detailed records, manual or electronic, of operations performed during the work shift.
* Active Participation in Factory Acceptance testing, Site Acceptance Testing and commissioning/qualification of equipment.
* Contribute to the development of batch records and electronic batch records for the site.
Requirements:
* A secondary education and 1 year's experience in GMP manufacturing are required.
* Prior experience in Batch processing operations in an FDA/ HPRA regulated industry is highly desirable.
* Essential: Annual visual test certification for color blindness and 20/20 vision is mandatory.
* Experience handling hazardous chemicals is highly advantageous.
* Prior Inspection experience in a Pharma/Biologics facility is beneficial for operators assigned to VI.