Validation and Quality background is needed, they need to have both. Sterilization validation would be a plus. Equipment validation is important. Lab equipment qualifications. Must work independently. Might be final approver for documents. Excel knowledge a plus. Reviewing and approving documents a major plus. Must be able to work with others as well. Fully onsite. Bachelor’s Degree/Undergraduate Degree in engineering or technical discipline. Master Degree preferred. Experience in pharmaceutical/biopharmaceutical industry or related industry/manufacturing environment. Ability to work on strict deadlines. Background in life science. Ability to interface with cross-functional teams. Detail oriented. Strong working knowledge of Quality System Regulations. Experience leading CAPA (Corrective and Preventive Action) activities. Ability to handle multiple projects concurrently. Well-developed communication skills, both verbal and written.. Years of Experience: 6 – 9 Years
br{display:none;}.css-58vpdc ul > li{margin-left:0;}.css-58vpdc li{padding:0;}]]> Title Systems Administrator Position Summary: The Systems Administrator (SA) is knowledgeable in all aspects of...
Apply For This Jobbr{display:none;}.css-58vpdc ul > li{margin-left:0;}.css-58vpdc li{padding:0;}]]> Job Title: Integration Technician – Medical systems and equipment Locations: Stamford, CT Duration: Full Time,...
Apply For This JobAbout the roleWe are seeking a Research Scientist II that is highly motivated, flexible and an adaptive team player for...
Apply For This Jobbr{display:none;}.css-58vpdc ul > li{margin-left:0;}.css-58vpdc li{padding:0;}]]> Greetings! Computer World Services is looking for experienced IT professionals to support the US Army...
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Apply For This JobJob Description5,600! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). NIBR is the innovation engine...
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