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2009 Summer Internship- Quality Operations - (US-VA-Elkton - 22827)
Minimum Education: Tech School Job Type: Full Time Email this job to yourself or to a friend | Job Match Test | Resume Guide
Click Here to Apply OnlineMerck & Co. Inc. established in 1891 is a global research-driven pharmaceutical company dedicated to putting patients first. Join us and experience our culture first-hand - one of strong ethics & integrity diversified experiences and a resounding passion for improving human health. As part of our global team youll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
The successful candidate will apply engineering science and business skills to help Merck carry out its core functions. A number of different entry points are possible for a new hire in our manufacturing division. Engineering at Merck has the vital role of bridging the gap between new pharmaceutical and vaccine discoveries and commercial products. Chemical processes produce in bulk form the high quality complex chemicals used in Mercks most valuable human health animal health and agricultural products. We then convert these basic chemicals into safe effective pharmaceuticals through formulation and packaging processes. Biologically derived products follow a similar path.
At Merck we believe you can develop faster if we give you real challenges right from the onset. In MMD we encourage you to move between functional groups so that you get hands-on experience in many aspects of our operations.
The intern will be responsible for all Quality related functions that directly support the VMF Integrated Process Team (IPT) and the site value stream map while actively supporting participating in and embracing an empowered team culture. Activities include but are not limited to the following:
Direct in-line Quality support for all compliance release and environmental monitoring matters; review and approval of electronic batch records; raw material components and finished/packaged product release; atypical investigations; change request submissions; SOP and CJA development and review; direct support of regulatory inspections and audits; conduct periodic shop floor audits to ensure compliance; direct support of validation activities and all other associated quality functions. Specific to Environmental Monitoring (EM) the coordinator will be responsible for maintaining the EM program to include the following: performing environmental sampling of aseptic areas personnel and utility systems; processing of microbial and chemical samples in the EM Laboratory; maintain and operate all laboratory testing equipment (incubators LAL TOC etc); report monitoring results via NGL; investigate OOS results and/or laboratory atypicals; evaluate environmental data for adverse trends; develop and participate in media challenges. This position is based in Durham NC.
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