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	<title>Life Science Staffing</title>
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	<link>http://lifesciencestaffing.com</link>
	<description>Medical Device, Biotechnology, Pharmaceutical</description>
	<lastBuildDate>Fri, 03 May 2013 22:29:48 +0000</lastBuildDate>
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		<title>Sr. Manufacturing Engineer &#8211; Central MA</title>
		<link>http://lifesciencestaffing.com/2013/05/sr-post-market-compliance-specialist-massachusetts/</link>
		<comments>http://lifesciencestaffing.com/2013/05/sr-post-market-compliance-specialist-massachusetts/#comments</comments>
		<pubDate>Fri, 03 May 2013 10:00:46 +0000</pubDate>
		<dc:creator>RP</dc:creator>
				<category><![CDATA[Quality]]></category>

		<guid isPermaLink="false">http://lifesciencestaffing.com/?p=455</guid>
		<description><![CDATA[Please contact us Directly 508-478-1413 or Apply through link on the right (US Job Openings). POSITION RESPONSIBILITIES: The Sr Manufacturing Engineer will be responsible for the development and optimization of processes and systems to support the overall Business Objectives. Areas of specific responsibility and attention include: o Develop manufacturing processes and measurement methods to meet [...]]]></description>
				<content:encoded><![CDATA[<p><em>Please contact us Directly 508-478-1413 or Apply through link on the right (US Job Openings).</em></p>
<p>POSITION RESPONSIBILITIES:<br />
The Sr Manufacturing Engineer will be responsible for the development and optimization of processes and systems to support the overall Business Objectives.<br />
 Areas of specific responsibility and attention include:<br />
o Develop manufacturing processes and measurement methods to meet tight tolerance manufacturing requirements<br />
o Design manufacturing fixtures and simple tooling<br />
o Specify requirements for manufacturing equipment<br />
o Conduct process evaluations utilizing tools such as SPC, DOE, and, MSA<br />
o Evaluation and improvement of process capabilities<br />
o Conduct root cause failure analysis and corrective action<br />
o Establish sampling plans / Quality plans<br />
o Participate / lead risk management activities including FMEA<br />
o Support reliability engineering activities<br />
o Participate / lead validation activity for design, process or products<br />
o Development and qualification of test methods for verifications and validations<br />
o Lead, support, and/or coach improvement projects throughout the life cycle of company products</p>
<p>EXPERIENCE: 5-7 years in the medical device industry or other regulated industry ie Defense, Automotive<br />
o Proven ability to solve problems and improve processes that use mechanical components<br />
o Good knowledge and experience with injection molding processes and components is required.<br />
o Successful implementation of statistical based quality improvement tools such as Design of Experiments, Statistical Process Control,<br />
  and Gage R&#038;R.<br />
o Project leadership in multi-disciplined projects.</p>
<p>EDUCATION:<br />
BS in Mechanical or related Engineering field is required.</p>
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