3cert Limited

&lt;p&gt;&lt;strong&gt;Location:&lt;/strong&gt; Malta, Germany and Hybrid (partly Home Office)&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Type of contract:&lt;/strong&gt; Full-time, Permanent&lt;/p&gt;
&lt;p&gt;3cert Ltd. is a &lt;strong&gt;&lt;em&gt;Certification Body&lt;/em&gt;&lt;/strong&gt; located in Malta and Germany, having international business relationships.&lt;br&gt;Currently, we are one step before becoming a &lt;strong&gt;&lt;em&gt;Notified Body&lt;/em&gt;&lt;/strong&gt; for MDR. Related to the new tasks we are now facing, we are looking for you – A person with experience in healthcare, medical device industry or certification / notification business.&lt;/p&gt;
&lt;p&gt;3cert Ltd. is young and dynamic company with the perks of a start-up, the benefits of a SME but without the common downsides of a small and fresh business.&lt;/p&gt;
&lt;h2 id=&quot;tasks&quot;&gt;Tasks&lt;/h2&gt;
&lt;p&gt;You will &lt;strong&gt;&lt;em&gt;support the Certification and Recognition Manager&lt;/em&gt;&lt;/strong&gt; in all tasks related to&lt;br&gt;notification. By that also come tasks in business development.  &lt;/p&gt;
&lt;p&gt;Moreover, you can &lt;strong&gt;&lt;em&gt;perform conformity assessment activities&lt;/em&gt;&lt;/strong&gt; (audits, technical documentation) according to ISO 13485 / MDR. Primarily, you will do the &lt;strong&gt;&lt;em&gt;assessment of technical documentation&lt;/em&gt;&lt;/strong&gt; of selected product groups in your field of&lt;br&gt;expertise.&lt;/p&gt;
&lt;h2 id=&quot;requirements&quot;&gt;Requirements&lt;/h2&gt;
&lt;p&gt;We are looking for you, when you are an open-minded and adaptive person with education and job experience in &lt;strong&gt;&lt;em&gt;healthcare / life sciences&lt;/em&gt;&lt;/strong&gt;. You know how to communicate appropriate to all levels within an organization, verbally and in writing. &lt;/p&gt;
&lt;p&gt;You must have a successful completion of a &lt;strong&gt;&lt;em&gt;university or technical college degree&lt;/em&gt;&lt;/strong&gt; or equivalent qualification in relevant studies, e. g. medicine, pharmacy, engineering or other relevant sciences. You also need at least &lt;strong&gt;&lt;em&gt;4 years of experience&lt;/em&gt;&lt;/strong&gt; in the field of healthcare products or related activities such as in quality management system, development, quality assurance, regulatory affairs, testing, research or use. &lt;/p&gt;
&lt;p&gt;You have knowledge and understanding of relevant legislation, guidance documents, norms, standards (e. g. Regulation EU 745/2017, MEDDEV documents, ISO 13485, ISO 17021). Therefore, it is a plus, when you have experience working in a notified body / certification body. &lt;/p&gt;
&lt;p&gt;When you are fluent in English (B2-C2 CEFR level), we would consider your&lt;br&gt;application. Fluency in German or other languages is a plus.&lt;/p&gt;
&lt;h2 id=&quot;benefits&quot;&gt;Benefits&lt;/h2&gt;
&lt;p&gt;Join us – a young, motivated and international team. We are, what we expect you to be: open-minded and adaptive.&lt;br&gt;Apart that we can grant you &lt;strong&gt;&lt;em&gt;flexible working times and part time home office&lt;/em&gt;&lt;/strong&gt;. You will see the world, as &lt;strong&gt;&lt;em&gt;traveling&lt;/em&gt;&lt;/strong&gt; and meeting new people and companies is part of your daily work. For that we can offer you excellent IT-infrastructure. You will receive a good, customary salary with &lt;strong&gt;&lt;em&gt;capital formation saving payments&lt;/em&gt;&lt;/strong&gt;. &lt;/p&gt;
&lt;p&gt;We can offer you a relocation package which includes a defined amount of money for the moving costs incurred (if applicable). Moreover, we offer you our assistance if you have any questions about your new living arrangements. &lt;/p&gt;
&lt;p&gt;We look forward to getting to know&lt;br&gt;you!&lt;/p&gt;
