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			<title>CAPEX API Project Manager </title>
			<link>http://contractjobs.ie/CAPEX-API-Project-Manager-Jobs-Tipperary-SMC92849</link>
			<description>
				We&amp;rsquo;re currently recruiting for a CAPEX API Project Manger to support a major pharmaceutical manufacturer based in Ballydine, Co. Tipperary.   This is a contract opportunity working on the delivery of API facility scope through design, construction, commissioning and qualification. The role will suit an experienced pharmaceutical project professional who has worked across large-scale GMP capital projects, ideally within API, drug substance, chemical synthesis or complex process manufacturing environments.    Duties  
  Coordinate delivery of API facility project scope...			</description>
			<pubDate>Wed,17 Jun 2026 08:30:00 </pubDate>
		</item>
			
		<item>
			<title>Tech Transfer Lead - Sterile Drug Product</title>
			<link>http://contractjobs.ie/Tech-Transfer-Lead-Sterile-Drug-Product-Jobs-Dublin-SMC03954</link>
			<description>
				We&amp;rsquo;re currently recruiting for an exciting opportunity with a Biopharmaceutical organization based in Dublin. 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.     Key Responsibilities:  
  Be accountable for success of the product transfer project from initiation to the transfer, through line characterisation, engineering studies, process performance qualification and ultimately to regulatory approval.  Provide solutions when trouble shooting drug substance freezing/thawing, formulation%2...			</description>
			<pubDate>Mon,02 Mar 2026 08:30:00 </pubDate>
		</item>
			
		<item>
			<title>Design Assurance Program Manager</title>
			<link>http://contractjobs.ie/Design-Assurance-Program-Manager-Jobs-Galway-TG-Program-Manager</link>
			<description>
				 Job title:  Design Assurance Program Manager  Location:  Ballybrit Upper Industrial Estate, Galway  Benefits:  Hourly rate contract, 3 days a week (Partime), Hybrid working   Company:   My client are a global leader in the medical device industry and expert in the design, development, and manufacturing of complex medical devices and component technologies.    Responsibilities:   &amp;bull; Lead Quality Representative on projects, directly contributing and/or providing guidance to others to establish appropriate Design History File / Device Master Record docume...			</description>
			<pubDate>Tue,25 Mar 2025 08:30:00 </pubDate>
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