<rss version="0.91">

<channel>
     <title>Pharmaceutical</title>
     <link>http://pharmaceutical.ie</link>
     <description></description>
     <language>en-us</language>

     <image>
         <title>Pharmaceutical</title>
         <url>http://pharmaceutical.ie/logo.png</url>
         <link>http://pharmaceutical.ie</link>
         <width>273</width>
         <height>53</height>
     </image>
	
		<item>
			<title>Associate Director External Supply </title>
			<link>http://pharmaceutical.ie/Associate-Director-External-Supply-Jobs-Dublin-SCA015670</link>
			<description>
				 Associate Director External Supply  Our client, a growing organisation in the AI-driven medical device sector is seeking an Associate Director of External Supply to partner with senior leadership in managing global, cross-functional operations across R&amp;amp;D, NPI, Manufacturing, and Supply. As Associate Director External Supply you will act as a key operational leader, ensuring effective coordination across internal teams and external partners while driving performance, compliance, and continuous improvement. This is a permanent role with hybrid working.   Res...			</description>
			<pubDate>Fri,17 Apr 2026 08:30:00 </pubDate>
		</item>
			
		<item>
			<title>Reg Affairs Specialist</title>
			<link>http://pharmaceutical.ie/Reg-Affairs-Specialist-Jobs-Connaught-TG-RA-Galway</link>
			<description>
				 Role:  Regulatory Affairs Engineer   Location:  Parkmore, Galway (Hybrid working)   Benefits:  Top salary       Company:   My client are a growing Medical Device company who have recently moved into a high tech new site in Parkmore. They have developed an innovative new technology to improve the performance of Vascular stents.          Role:    Reporting to the Senior Regulatory Affairs Manager, as a Regulatory Affairs Specialist you will play a key a key role in the implementation of post-market activities within Veryan. This is a ...			</description>
			<pubDate>Fri,13 Jun 2025 08:30:00 </pubDate>
		</item>
			
		<item>
			<title>Quality Specialist</title>
			<link>http://pharmaceutical.ie/Quality-Specialist-Jobs-Republic-of-Ireland-TG-QE-Shannon</link>
			<description>
				 Job title:  Quality Assurance Specialist   Location:  Western Business Park, Shannon, Co. Clare   Benefits:  Good salary, Healthcare, pension, 25 days holidays, opportunity to grow your career with exciting Medical Device company working on projects from concept.       Summary:   The Quality Systems specialist role will involve supporting the development and implementation of the Quality Management System with my Medical Device client in order to maintain 2017/745(MDR), ISO 13485, ISO 14971, ISO 9001 and FDA QSR standards and requirements. The QMS includes m...			</description>
			<pubDate>Fri,07 Feb 2025 08:30:00 </pubDate>
		</item>
			
		<item>
			<title>Quality Specialist</title>
			<link>http://pharmaceutical.ie/Quality-Specialist-Jobs-Republic-of-Ireland-TG-QE-Shannon</link>
			<description>
				 Job title:  Quality Assurance Specialist   Location:  Western Business Park, Shannon, Co. Clare   Benefits:  Good salary, Healthcare, pension, 25 days holidays, opportunity to grow your career with exciting Medical Device company working on projects from concept.       Summary:   The Quality Systems specialist role will involve supporting the development and implementation of the Quality Management System with my Medical Device client in order to maintain 2017/745(MDR), ISO 13485, ISO 14971, ISO 9001 and FDA QSR standards and requirements. The QMS includes m...			</description>
			<pubDate>Tue,28 Jan 2025 08:30:00 </pubDate>
		</item>
			
		<item>
			<title>Quality Specialist</title>
			<link>http://pharmaceutical.ie/Quality-Specialist-Jobs-Republic-of-Ireland-TG-QE-Shannon</link>
			<description>
				 Job title:  Quality Assurance Specialist   Location:  Western Business Park, Shannon, Co. Clare   Benefits:  Good salary, Healthcare, pension, 25 days holidays, opportunity to grow your career with exciting Medical Device company working on projects from concept.       Summary:   The Quality Systems specialist role will involve supporting the development and implementation of the Quality Management System with my Medical Device client in order to maintain 2017/745(MDR), ISO 13485, ISO 14971, ISO 9001 and FDA QSR standards and requirements. The QMS includes m...			</description>
			<pubDate>Thu,16 Jan 2025 08:30:00 </pubDate>
		</item>
		</channel>
</rss>
