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			<title>Senior Operational Readiness Associate  </title>
			<link>http://contractjobs.ie/Senior-Operational-Readiness-Associate-Jobs-Dublin-RK5485</link>
			<description>
				Senior Operational Readiness Associate  Hybrid RK5485 Contract 12 months Dublin     We&amp;rsquo;re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical 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.      This role will monitor compliance and adherence metrics (e.g., milestone readiness, action closure, training and documentation status), provide timely visibility to leadership, and escalate risks, gaps, or non-conforman...			</description>
			<pubDate>Mon,13 Jul 2026 08:30:00 </pubDate>
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			<title>Senior Operational Readiness Associate  </title>
			<link>http://contractjobs.ie/Senior-Operational-Readiness-Associate-Jobs-Dublin-RK3553</link>
			<description>
				Senior Operational Readiness Associate  Hybrid RK3553 Contract 12 months Dublin     We&amp;rsquo;re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical 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.      This role will monitor compliance and adherence metrics (e.g., milestone readiness, action closure, training and documentation status), provide timely visibility to leadership, and escalate risks, gaps, or non-conforman...			</description>
			<pubDate>Mon,22 Jun 2026 08:30:00 </pubDate>
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			<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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