{"id":42826,"date":"2023-10-11T11:01:36","date_gmt":"2023-10-11T10:01:36","guid":{"rendered":"https:\/\/lscconnect.com\/consultantconnect\/jobs\/qa-specialist\/"},"modified":"2023-10-11T11:01:37","modified_gmt":"2023-10-11T10:01:37","slug":"qa-specialist-42826","status":"publish","type":"wpbb_job","link":"https:\/\/lscconnect.com\/consultantconnect\/jobs\/qa-specialist-42826\/","title":{"rendered":"QA Specialist"},"content":{"rendered":"<p> <strong>LSC have a great contract opportunity for QA Specialist to join a Cork based biopharma company. <\/strong><br \/> <strong>ABOUT THE PROJECT &#8211; KEY RESPONSIBILITIES:<\/strong><\/p>\n<ul>\n<li>Batch Record Review &amp; material release to ensure compliance with GMP requirements.<\/li>\n<li>Review &amp; Approval of Event, Deviations, and Customer complaints.<\/li>\n<li>Supports all validation activities on site as described in the Site Validation Master Plan<\/li>\n<li>Carries out tasks related to the administration of site supplier approval process.<\/li>\n<li>Co-ordinates and assists in the preparation for regulatory and customer GMP inspections of the site<\/li>\n<\/ul>\n<p><strong>ABOUT YOU &#8211; ARE YOUR SKILLS A MATCH?<\/strong><\/p>\n<ul>\n<li>Experience as Quality Assurance Specialist in QA Operations, 3-5 experience in a quality, validation or compliance role within the biological and\/or pharmaceutical industry.<\/li>\n<li>Bachelor&#8217;s degree in a scientific\/technical discipline required<\/li>\n<li>Experience in auditing of external suppliers, contractors, and vendors<\/li>\n<\/ul>\n<p><strong>Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G\/Stamp 4 visa to apply!<\/strong><\/p>\n<p><strong>Apply via this advert or contact Grainne Hodnett at +353 214771329 if you have any more questions about this opportunity!<\/strong><\/p>\n<p><img decoding=\"async\" src=\"https:\/\/counter.adcourier.com\/a2NvdWdobGFuLjI1MjEwLjEyMzg4QGxzY2x0ZC5hcGxpdHJhay5jb20.gif\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>LSC have a great contract opportunity for QA Specialist to join a Cork based biopharma company. ABOUT THE PROJECT &#8211; KEY RESPONSIBILITIES: Batch Record Review &amp; material release to ensure compliance with GMP requirements. Review &amp; Approval of Event, Deviations, and Customer complaints. 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