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<table width="370" border="0" cellspacing="0" cellpadding="0"> <tr> <td class="greytext"> <strong><span class="greentext">Regulatory Manager</span></strong></p> <strong>Location:</strong> Libertyville, IL.</p> <strong>General Description:</strong> <br> Preparation of document packages and compiling material for US EPA, Canadian (PMRA) and state <br>regulatory submissions (including new product applications, re-registrations, new uses, fee payments, sub-registrations, amendments to labels & confidential statements of formula (CSFs) and other regulatory actions). Provide regulatory advice and support to sales and marketing and customers (including label reviews for <br>sub-registrations & "me-too" kits). Recommend changes in labeling for regulatory compliance. Prepare, <br>amend, and submit labels and CSFs in accordance with FIFRA and state regulatory requirements. <br>Coordinate, schedule and track ESD amendments, notifications and new product applications. Coordinate <br>EPA registration fee payments and prepare and submit annual EPA production reports and maintenance fees. Monitor and improve tracking/control systems. Direct interaction with regulatory agencies on defined matters. Communicate to regulatory manager timelines for achievement of registrations. Work with various internal <br>groups (development, sales, and marketing) and external customers. Exercise professional judgment to <br>resolve critical issues to support the business.<br><br>Principal Responsibilities: <br> Prepare applications for registration and re-registration of pesticide products with US EPA, Canadian (PMRA) and the California Department of Pesticide Regulation.<br> Provide advice to sales & marketing to assist customers in obtaining alternate formulations &<br> additional label claims or answer other regulatory questions as needed.<br> Maintain department internal files for all products.<br> Work with Research & Development to provide required information for new and amended <br> formulations and labels.<br> Travel and represent the company with externals entities when required.<br> Communicate with government officials to facilitate product registration approvals.<br><br>Experience: <br> Minimum of 3-5 years of regulatory experience in a Life Sciences field, or related experience. <br>Education: <br> College degree required, BS degree preferred <br> Other: <br> Travel by air and car (up to 20%). <br><br>We will only contact you when scheduling an interview.<br></p> </td> </tr> </table>
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