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QA Specialist
US-CA-Union City
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<div> <p><b>Title: </b>QA Specialist</p> <p><b>City: </b>Union City</p> <p><b>State:</b> CA</p> <p><b>ZIP:</b> 94587</p> <p><b>Job Type</b>: Temp2Hire</p> <p><b>Shift(s):</b> Monday - Friday</p> <p><b>Hours: </b>10:00 am 7:00 pm</p> <p><b>Pay Rate:</b> $30-40 DOE</p> <p><b>Job Code:</b> JPC-4197</p> <p><b><u>Background check and drug screen required.</u></b><u> </u></p> <p><br /> Tekberry is looking for a highly qualified and motivated <b>QA Specialist </b>to work on-site with our client, the world's largest producer of medicine and vaccinations for pets and livestock. As a QA Specialist, you'll assist and support the organization with initial compliance and ongoing preparation, testing and monitoring of conformance to established quality assurance processes and standards for manufacturing and production. Performs evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards. Identifies risk and evaluates deficiencies while working with internal departments/business units to appropriately remedy them. Facilitates internal training on quality assurance requirements, processes, and procedures. May perform audits and risk assessments. W2 employee you will have access to health benefits. </p> <p><b>Responsibilities:</b></p> <ul> <li>Perform in-depth and thorough Device History Record (DHR) reviews and disposition all Abaxis products in compliance with established release procedures. Be alert to developing trends and proactively notify manager and Quality management of emerging issues</li> <li>Generate Certificates of Analysis and Certificates of Conformance for all Abaxis products.</li> <li>Organize and maintain Device History Records.</li> <li>Address issues with Device History Records (DHRs) in a timely manner. Demonstrate appropriate professional communication when interfacing with production personnel to resolve any documentation issues in DHRs.</li> <li>Process ERP transactions to segregate and disposition non-conforming product.</li> <li>Assist with developing, reviewing and improving procedures and processes related to product quality.</li> <li>Assist with internal and external audits.</li> <li>Other duties and responsibilities in the Quality department, as assigned.</li> </ul> <p><b>Qualifications:</b></p> <ul> <li>BS in Chemistry or Biochemistry or any other scientific discipline with relevant experience.</li> <li>Strong attention to details and ability to understand and follow complex procedures.</li> <li>Strong technical skills including basic statistical analysis.</li> <li>Sound working knowledge of regulations pertaining to QA and related compliance requirements.</li> <li>Working knowledge and experience in basic computer applications such as</li> <li>Microsoft Word, Excel and Outlook. Experience in Visio is preferred.</li> <li>Effective and clear written and verbal communication skills.</li> </ul> <p>Tekberry Inc. is an equal opportunity employer. US citizens, Green Card Holders and those authorized to work in the US are encouraged to apply. We are unable to work Corp to Corp or to sponsor H-1B visas currently. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.</p> </div> <table> </table>

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