Compliance Specialist

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          "text": "<p>Review of Quality Critical Alarms and NRSR</p><p>Review J&amp;Cs</p><p>Metric entry into database</p><p>Initiate and investigate deviations for non-conformance</p><p>Conduct deviation containment assessment (off-hour support)</p><p>Provide off-hour support for batch record issuance</p><p>Function as back-up for QA Manager</p><p>Other activities as assigned</p><p> </p><p><strong>QUALIFICATIONS</strong>:</p><p>An ongoing commitment to conducting our global business according to the highest legal and ethical standards,</p><p>and to continually pursue excellence in the development and delivery of all of our products and services. This</p><p>includes:</p><p>Adhering to all applicable laws and regulations of the places in which we conduct business, as well as our</p><p>own Company policies and procedures.</p><p>Being honest and treating people with respect and courtesy.</p><p>Constantly striving to make Genzyme a great place to work, and a company respected for the quality of its</p><p>people and products.</p><p>Acting as role models for our fellow employees by acting responsibly, fairly, and honestly in our dealings and</p><p>exercising sound judgment in performing our jobs.</p><p> </p><p><strong>BASIC QUALIFICATIONS:</strong></p><p>Bachelor’s Degree in a scientific field and 4-6 years experience in a Quality and /or other cGMP related field,</p><p>or Master’s Degree in a scientific field and 2 years’ experience in above.</p><p>2 years of experience in a Quality role.</p><p>Knowledge in external agency regulations (FDA, EMA, etc.)</p><p>Strong computer, verbal and written communication skills.</p><p>Experience in quality systems.</p><p>Experience in leading cross functional team.</p><p>Experience with Track wise or equivalent system.</p><p>Proficient in Microsoft Office.</p>",
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