{"id":37524,"date":"2023-07-04T10:53:02","date_gmt":"2023-07-04T09:53:02","guid":{"rendered":"https:\/\/lscconnect.com\/consultantconnect\/jobs\/qa-specialist\/"},"modified":"2023-07-26T09:48:57","modified_gmt":"2023-07-26T08:48:57","slug":"qa-specialist-37524","status":"publish","type":"wpbb_job","link":"https:\/\/lscconnect.com\/consultantconnect\/jobs\/qa-specialist-37524\/","title":{"rendered":"QA Specialist"},"content":{"rendered":"<p><strong>LSC have a great contract opportunity for a QA Specialist to join a top 10 Pharmaceutical company based in Tipperary. The site supports the complete pharmaceutical small molecule process for Phase III clinical to product release and market support. On site processes include API manufacture, formulation, OSD tableting, packaging and global logistics &amp; distribution. The facility takes in raw chemicals and ships finished medicines to end users. This site has grown from an API site to a strategically important campus that supports critical stages of the company&#8217;s drug lifecycle. <\/strong><\/p>\n<p><strong>If you have a degree in Science or Quality and are ready for your next challenge, this could be the perfect project for you!<\/strong><\/p>\n<p><strong>ABOUT THE PROJECT &#8211; KEY RESPONSIBILITIES:<\/strong><\/p>\n<ul>\n<li>Makes decisions within guidelines and policies which impact own priorities and allocation of time to meet deadlines.<\/li>\n<li>Supports Corporate Quality to ensure actions related to Quality Systems and\/or Operational Quality at the site are executed.<\/li>\n<li>Participation in inspections of Site by Divisional \/ Regulatory Bodies \/ third parties together with follow up actions where applicable.<\/li>\n<li>Ensure supply of high quality product through the implementation and oversight of the Quality Management System for the site.<\/li>\n<li>Ensure the highest Quality, Compliance and Safety standards.<\/li>\n<li>The Associate Specialist\/ Specialist will participate and comply with the MMD Quality Management System (QMS) requirements, including ownership.<\/li>\n<\/ul>\n<p><strong> ABOUT YOU &#8211; ARE YOUR SKILLS A MATCH?<\/strong><\/p>\n<ul>\n<li>1 &#8211; 5 years&#8217; experience in the Pharmaceutical industry or a similar operating environment which includes experience in a Quality function<\/li>\n<li>Demonstrated knowledge in more than one pharmaceutical and\/or chemical manufacturing operation (i.e. Quality, science etc.)<\/li>\n<li>Operational experience of at least 4 QMSs<\/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 Gr\u00e1inne Hodnett on 021 4777 329 if you have any more questions about this opportunity!<\/strong><\/p>\n<p><img decoding=\"async\" src=\"https:\/\/counter.adcourier.com\/a2NvdWdobGFuLjczNDgyLjEyMzg4QGxzY2x0ZC5hcGxpdHJhay5jb20.gif\" \/><\/p>\n","protected":false},"excerpt":{"rendered":"<p>LSC have a great contract opportunity for a QA Specialist to join a top 10 Pharmaceutical company based in Tipperary. The site supports the complete pharmaceutical small molecule process for Phase III clinical to product release and market support. On site processes include API manufacture, formulation, OSD tableting, packaging and global logistics &amp; distribution. 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