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			<title>CQV Engineer</title>
			<link>http://contractjobs.ie/CQV-Engineer-Jobs-Roscommon-AS00003</link>
			<description>
				We&amp;rsquo;re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Athlone. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.   The CQV Engineer will be responsible for life cycle qualification documentation. This specific role is for Process Equipment in a solid dosage environment. They will work with the Equipment Project Lead to ensure the system is commissioned and qualified as expected. The role is client-side, and will be accountable for c...			</description>
			<pubDate>Fri,21 Aug 2026 08:30:00 </pubDate>
		</item>
			
		<item>
			<title>Senior Commissioning and Qualification Lead</title>
			<link>http://contractjobs.ie/Senior-Commissioning-and-Qualification-Lead-Jobs-Roscommon-SMC92874</link>
			<description>
				We&amp;rsquo;re currently recruiting for an exciting opportunity with an award winning pharmaceutical organization based in Athlone. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.    Duties  
  Develop and own the Commissioning, Qualification &amp;amp; Validation (CQV) strategy and execution plan for the project, aligned to project schedule and GMP requirements up to Performance Qualification of all systems and equipment. Act as Client C&amp;amp;Q Lead onsite throughout execution; coordinate all co...			</description>
			<pubDate>Thu,21 May 2026 08:30:00 </pubDate>
		</item>
			
		<item>
			<title>Reg Affairs Specialist</title>
			<link>http://contractjobs.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>
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