Senior Global PV Compliance Manager & Deputy EU/UK QPPV

<p>Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.</p><p></p><p>We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.</p><p></p><p></p><h2>As<span> </span><b>Senior<span> </span>Global<span> </span>PV<span> </span>Compliance<span> </span>Manager &amp; Deputy EU/UK QPPV,</b><span> </span>you will be responsible for<span> </span>global<span> </span>PV<span> </span>Compliance, supporting the development and maintenance of GPS Quality<span> </span>Management<span> </span>System, with oversight of GPS training strategy. A crucial part of the position will be leading and facilitating GvP audit and inspection activities, as well as supporting<span> </span>management<span> </span>of GPS<span> </span>global<span> </span>PV agreements.</h2><p></p><p>Moreover, you will be serving as the Deputy Qualified Person for<span> </span>Pharmacovigilance<span> </span>for the European Union (EU QPPV) and UK QPPV working closely with the EU/UK <span>QPPV.                 </span></p><p>Reporting to the EU/UK QPPV and Head of Benefit Risk &amp;<span> </span>Global<span> </span>PV<span> </span>Compliance, within the wider<span> </span>Global<span> </span>Patient<span> </span>Safety<span> </span>team, you will be managing a close team of experts based in the EU and US.  Occasional international travel on an ad-hoc basis is to be expected.</p><p>We are open to applicants from all EU countries. </p><p></p><h2><b>What you’ll be doing</b></h2><ul><li>Acts as the contact person for the Competent Authorities for medical<span> </span>safety<span> </span>requests/questions. regarding a medicinal product licensed in the EU/UK in the absence of the QPPV.  Together with QPPV acts as a single contact point for the Competent Authorities on a 24-hour basis.</li><li>Overviews<span> </span>safety<span> </span>profiles, knowledge of any emerging<span> </span>safety<span> </span>concerns and any other information relating to evaluation of the risk-benefits of the medicinal products for which Vantive holds authorizations in the EU/UK. </li><li>Maintaining access to a medical doctor for the assessment of medical emergencies, case evaluations,<span> </span>safety<span> </span>signal proportionality or benefit-risk assessments. Review and support PV benefit-risk content sections of drug therapeutic product labeling.</li><li>Lead preparation and conduct of PV audits and inspections, ensuring that all stakeholders are properly trained in<span> </span>compliance<span> </span>and inspection readiness needs.</li><li>Responsible for managing and facilitating audits and inspections, providing adequate CAPA handling of the observations available in audit reports.</li><li>Accountable for the proper<span> </span>management<span> </span>of GPS QMS documents and has oversight responsibility for GPS<span> </span>Pharmacovigilance<span> </span>global<span> </span>processes.</li><li>Manages the GPS training process. </li><li>Supervises and manages the GPS<span> </span>global<span> </span>PV agreement process <span>                                                                                                                                                                                     </span></li></ul><h2><b>What you’ll bring</b></h2><ul><li>Bachelor´s degree minimum in a medical or scientific field, with proven experience in<span> </span>Global<span> </span>Pharmacovigilance, specifically<span> </span>compliance, working in a<span> </span><span>global-regional-local</span> patient<span> </span>safety<span> </span>model where two-way direct communication has been required to ensure functional alignment<span> </span>globally.</li><li>Excellent leadership and interpersonal skills demonstrated through successfully leading and driving PV audits and inspection processes, in particular Regulatory Authority Inspections (i.e EMA, MHRA, FDA, Chinese HA, PMDA and TGA).</li><li>Successfully demonstrated people<span> </span>management<span> </span>experience as well as ability to motivate, lead and develop a multicultural team</li><li>Outstanding analytical and problem-solving skills proven through ex