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<workzag-jobs>

<position>
    <id>2595433</id>
    <subcompany>CENTOGENE Brazil</subcompany>
    <office>Brazil - Sao Paulo</office>
    <department>Wet Lab</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Analista de Laboratório Sênior</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Receber, conferir e registrar amostras biológicas (sangue, embriões, swab e líquido amniótico) no sistema laboratorial, garantindo rastreabilidade e conformidade com os critérios pré-analíticos.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Realizar triagem, identificação e cadastro de amostras em sistemas informatizados, conforme protocolos estabelecidos.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Executar extração, quantificação e controle de qualidade de DNA a partir de amostras biológicas.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Realizar técnicas de biologia molecular, como PCR e NGS (sequenciamento de nova geração).</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Apoiar na análise de dados genéticos, interpretação de resultados e elaboração de laudos técnicos.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Garantir o cumprimento dos protocolos de qualidade, biossegurança e rastreabilidade das amostras.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Manter registros laboratoriais precisos e atualizados.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Participar de validações, controles internos de qualidade e auditorias.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Contribuir com a atualização de procedimentos operacionais padrão (POPs).</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Garantir o uso adequado de recursos e insumos, incluindo controle de estoque.</span></p>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Ensino superior completo em Biomedicina, Biologia, Farmácia ou áreas correlatas.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Experiência prévia em laboratório de biologia molecular.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Vivência com técnicas de PCR e NGS.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Conhecimento em extração e análise de DNA.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Familiaridade com rotinas de controle de qualidade e biossegurança.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Desejável experiência com análise de dados genéticos e elaboração de laudos.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">Diferenciais:</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Pós-graduação ou especialização em genética, biologia molecular ou áreas afins.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Experiência em laboratórios de diagnóstico genético.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Vivência com auditorias e acreditações laboratoriais</span></p><br>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[<p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;">· Vale Refeição: R$ 40,00 por dia</p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;">· Vale Alimentação: R$ 298,00 por mês</p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;">· Vale Transporte (sem desconto para o colaborador)</p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;">· Seguro saúde Bradesco (cobertura apenas para o titular)</p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;">· Day off no aniversário</p>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>2-5</yearsOfExperience>
    <occupation>other</occupation>
    <occupationCategory>other</occupationCategory>
    <createdAt>2026-04-09T10:07:57+00:00</createdAt>
</position>

<position>
    <id>2670300</id>
    <subcompany>CENTOGENE Germany GmbH</subcompany>
    <office>Germany - Rostock</office>
    <department>Research &amp; Development</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Analytical Chemist/ Biologist</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<ul><li>Implementation of bioanalytical methods to quantify metabolites, proteins or enzymatic activities in human specimen</li><li>Validation of these methods in accordance with international guidelines such as ICH M10</li><li>Literature research of newest technologies and approaches available</li><li>Laboratory work:<ol><li>tuning of assay parameters such as sample extraction protocol, LC-MS parameters or ELISA protocols. (This includes the preparation of solutions and buffers)</li><li>trouble shooting in case of instrumental failures</li></ol></li><li>Office work: Writing of work instructions, validation plans and reports as well as updates on project status to the customer</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<ul><li>Finished degree (Master+) in Chemistry or Biology</li><li>Experience with Liquid Chromatography and Mass Spectrometry</li><li>Optional: Experience with ELISA, Western Blot etc.</li><li>Knowledge of biochemistry, metabolomics and proteomics</li><li>Optional: Knowledge of genetics</li><li>Handling of pipettes and human specimens</li><li>Experience in scientific writing</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[<ul><li>Talents are individually supported by internal and external trainings</li><li>An international career in a multicultural environment</li><li>Regular company events form us as one team</li><li>Fitness area available for free + Gym cooperation with cleverfit Rostock</li><li>Corporate benefits</li><li>Food Spot</li><li>Bike leasing</li><li>Support of the job tickets (Deutschlandcard)</li><li>In case of language barriers we offer German and English classes</li><li>relocation support</li><li>Fruit baskets and various hot drinks for free</li><li>Precaution and financial protection guaranteed by company pension scheme</li></ul>Applications from severely disabled people with appropriate suitability are explicitly welcome. Severely disabled applicants and equivalent status are given preferential consideration in the event of equal qualification.]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>1-2</yearsOfExperience>
    <keywords>LC-MS,Liquid Chromatography ,genetics,fulltime,sample extraction ,human specimens</keywords>
    <occupation>healthcare_aid</occupation>
    <occupationCategory>medical_and_health</occupationCategory>
    <createdAt>2026-06-12T15:39:07+00:00</createdAt>
</position>

<position>
    <id>2340886</id>
    <subcompany>CENTOGENE Germany GmbH</subcompany>
    <office>Taiwan - Taoyuan City - EUR</office>
    <department>Marketing</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Customer Service Specialist – APAC</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<ul><li>Act as the first-line contact for customer inquiries, providing professional and timely support via phone, email, and online systems.</li><li>Support physicians, hospitals, and research partners with test ordering, sample logistics, and reporting processes.</li><li>Ensure smooth communication between clients in APAC and global teams, particularly HQ in Germany.</li><li>Manage case documentation, track service tickets, and update records in CENTOGENE’s internal systems (CRM, LIMS, etc.).</li><li>Provide guidance on test catalog, sample requirements, and logistics procedures.</li><li>Handle complaints and escalations in line with company policies, ensuring customer satisfaction.</li><li>Collaborate with cross-functional teams (sales, logistics, laboratory operations, and IT) to resolve client issues.</li><li>Prepare regular service reports and feedback summaries to improve customer experience.</li><li>Support training and onboarding for new customer service team members as the APAC office grows.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<ul><li>Bachelor’s degree in Life Sciences, Healthcare, Business Administration, or related field.</li><li>At least 5 years of experience in customer service or client-facing roles (preferably in healthcare, diagnostics, or biotech).</li><li>Strong communication skills in Mandarin Chinese and English (written and spoken).</li><li>Excellent problem-solving and multitasking abilities.</li><li>Familiarity with customer management systems (CRM, LIMS, ERP) is highly desirable.</li><li>Detail-oriented with a customer-first mindset.</li></ul>Preferred / Plus:<ul><li>Experience in the healthcare or diagnostics industry.</li><li>Familiarity with LDT regulations and laboratory workflows.</li><li>Experience working in an international or cross-cultural environment.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[<ul><li>Competitive compensation and benefits package.</li><li>Opportunity to support the growth of CENTOGENE’s first APAC operations in Taiwan.</li><li>Work in a dynamic, international, and mission-driven environment.</li><li>Professional development and career advancement opportunities.</li><li>Collaboration with global experts in genetics, bioinformatics, and diagnostics.</li></ul>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>5-7</yearsOfExperience>
    <occupation>retail_customer_service</occupation>
    <occupationCategory>customer_support_and_client_care</occupationCategory>
    <createdAt>2025-09-17T09:45:24+00:00</createdAt>
</position>

<position>
    <id>2309964</id>
    <subcompany>Extern</subcompany>
    <office>Taiwan - Taoyuan City - EUR</office>
    <department>DX Business</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Director – Genetic Testing, Reproductive Medicine (APAC)</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[We are seeking a senior leader to serve as Director of Genetic Testing in Reproductive Medicine for the Asia-Pacific (APAC) region. Reporting directly to the CEO, APAC, this role will be responsible for driving the growth, clinical excellence, and strategic development of our genetic testing portfolio in reproductive medicine across diverse markets in the region.<br> <br>The Director will combine deep expertise in genetics and reproductive health with strong commercial and operational leadership. They will act as a key member of the APAC leadership team, contributing to regional strategy and ensuring that our solutions are clinically relevant, commercially successful, and accessible to patients and providers.<br> <br><strong>Key Responsibilities</strong><br> <br>Strategic &amp; Business Leadership<ul><li>Define and implement the APAC strategy for genetic testing in reproductive medicine, aligned with global objectives.</li><li>Serve as a senior advisor to the CEO, APAC, on market dynamics, opportunities, and risks.</li><li>Lead cross-functional regional initiatives to scale genetic testing solutions, ensuring both clinical excellence and commercial success.</li></ul>Market Development &amp; Growth<ul><li>Drive adoption of genetic testing solutions (e.g., PGT, carrier screening, NIPT) across IVF clinics, hospitals, and healthcare networks.</li><li>Build and strengthen partnerships with fertility centers, KOLs, and policymakers to expand market presence.</li><li>Oversee product launches and go-to-market strategies tailored to the regulatory and cultural context of each APAC market.</li></ul> <br>Scientific &amp; Clinical Leadership<ul><li>Ensure high standards of clinical quality, compliance, and ethical practices in all genetic testing services.</li><li>Collaborate with global R&amp;D and medical affairs teams to adapt innovations for local needs.</li><li>Act as a thought leader, representing the company at regional scientific and industry forums.</li></ul>Operational &amp; Team Leadership<ul><li>Lead and inspire a cross-functional regional team spanning medical, commercial, and operational functions.</li><li>Manage P&amp;L accountability for the genetic testing business in reproductive medicine across APAC.</li><li>Establish metrics and governance processes to ensure sustainable performance.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<strong>Qualifications &amp; Experience</strong> <br><ul><li>Advanced degree (MD, PhD, MSc, MBA, or equivalent) in Genetics, Molecular Biology, Reproductive Medicine, or related field.</li><li>12+ years of experience in genetic testing, reproductive medicine, diagnostics, or biotech, with at least 5 years in a senior leadership role.</li><li>Demonstrated success in leading business units or major product lines in APAC healthcare or diagnostics markets.</li><li>Strong understanding of genetic testing technologies (NGS, cytogenetics, PGT, carrier screening, NIPT).</li><li>Proven ability to build partnerships with fertility centers, regulators, and healthcare stakeholders.</li><li>Track record of P&amp;L ownership, business growth, and organizational leadership.</li><li>Fluency in English required; additional Asian languages a strong advantage</li></ul>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>7-10</yearsOfExperience>
    <occupation>general_and_other_sales_and_business_development</occupation>
    <occupationCategory>sales_and_business_development</occupationCategory>
    <createdAt>2025-08-25T16:59:07+00:00</createdAt>
</position>

<position>
    <id>2636855</id>
    <subcompany>CENTOGENE Spain</subcompany>
    <office>Spain - Valencia</office>
    <department>IT</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Functional Consultant D365 Finance &amp; Supply Chain Management</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<h1><span style="font-size:18px;">The Project</span></h1><br>Centogene is expanding its corporate ERP, Microsoft Dynamics 365 — already deployed and operational at the parent company — to between 5 and 10 international subsidiaries. The functional scope covers Finance (General Ledger, Accounts Payable, Accounts Receivable) and basic Supply Chain Management (Procurement, Sales, Inventory Management), with a strong focus on intercompany processes.<br>A central element of this project is building a standardised and replicable implementation model that enables rapid and consistent rollouts to each new subsidiary, supported by local partners in each region. This is not just about implementing D365: it is about designing the way Centogene implements D365.<br><br><br><h1><span style="font-size:18px;">What We Are Looking For</span></h1><br>A professional with a strong functional profile and business vision, capable of engaging with stakeholders at each subsidiary to understand their processes, define requirements, and translate them into solutions within D365. This is not a development role, but we do need someone with sufficient technical grounding to be autonomous: someone who understands the D365 architecture, can navigate the configuration, and does not depend on the technical team for every decision.<br><br><h1><span style="font-size:18px;">Key Responsibilities</span></h1><ul><li>Lead the functional analysis at each subsidiary: requirements gathering, AS-IS process mapping, and TO-BE process design within D365.</li><li>Contribute to the design of the standard implementation model from a business perspective, identifying what is common across all subsidiaries and what requires local adaptation.</li><li>Act as the primary liaison between each subsidiary’s business teams and the project’s technical team.</li><li>Define and document intercompany processes between the parent company and subsidiaries in collaboration with the finance teams.</li><li>Coordinate with local partners on the execution of functional tasks, ensuring quality and consistency with the standard model.</li><li>Design and execute User Acceptance Testing (UAT) plans with key users.</li><li>Manage training and change management at each subsidiary.</li><li>Produce functional documentation and user manuals.</li><li>Participate in post go-live incident resolution and stabilisation.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<h1><span style="font-size:18px;">Essential Requirements</span></h1><ul><li>Proven experience in at least 2 full D365 Finance &amp; Supply Chain Management implementations in a functional role, preferably in multi-entity or multi-country projects.</li><li>Deep knowledge of Finance business processes (accounting, accounts payable/receivable, period-end closings) and basic Supply Chain (procurement cycle, sales, inventory management).</li><li>Experience defining and configuring intercompany processes.</li><li>Ability to engage with business stakeholders at different levels (from subsidiary controllers to financial leadership).</li><li>Sufficient knowledge of D365 technical architecture to be autonomous in configuration and decision-making.</li><li>Experience working with or coordinating implementation partners.</li><li>Fluent in Spanish and English.</li><li>Willingness to travel occasionally to international subsidiaries (kick-offs and go-lives).</li></ul><br><h1><span style="font-size:18px;">Desirable Requirements</span></h1><ul><li>Experience designing replicable implementation models, playbooks, or rollout templates.</li><li>Microsoft certification in D365 Finance or Supply Chain Management.</li><li>Experience in change management or end-user training.</li><li>Experience in the healthcare, biotech, or pharmaceutical sector.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[Centogene is a global leader in genetic diagnostics and precision medicine, founded in 2006 and headquartered in Rostock, Germany. With presence in over 100 countries, approximately 450 employees across 5 continents, and one of the largest genetic databases in the world, Centogene transforms clinical, genetic, and biochemical data into medical solutions for patients. Recently backed by Charme Capital Partners, the company is undergoing a phase of transformation and global growth.<br><br><h1><span style="font-size:18px;">What We Offer</span></h1><ul><li>Join a strategic, global-scale project at a leading precision medicine company.</li><li>Competitive salary: 60,000 – 90,000€ gross per annum, depending on experience.</li><li>Based in Valencia, Spain, with a hybrid working model.</li><li>Occasional international travel for kick-offs and go-lives.</li><li>The opportunity to design the group’s ERP expansion model from scratch.</li><li>A multicultural and innovative working environment.</li></ul>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>freelance</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>2-5</yearsOfExperience>
    <occupation>desktop_service_and_support</occupation>
    <occupationCategory>it_software</occupationCategory>
    <createdAt>2026-05-18T11:47:32+00:00</createdAt>
    <salaryInformation>
        <min>60000.00</min>
        <max>90000.00</max>
        <currencySymbol>€</currencySymbol>
        <currencyCode>EUR</currencyCode>
        <type>yearly</type>
    </salaryInformation>
</position>

<position>
    <id>2636879</id>
    <subcompany>CENTOGENE Spain</subcompany>
    <office>Spain - Valencia</office>
    <department>IT</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Functional-Technical Consultant D365 Finance &amp; Supply Chain Management</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<h1><span style="font-size:18px;">The Project</span></h1><br>Centogene is expanding its corporate ERP, Microsoft Dynamics 365 — already deployed and operational at the parent company — to between 5 and 10 international subsidiaries. The functional scope covers Finance (General Ledger, Accounts Payable, Accounts Receivable) and basic Supply Chain Management (Procurement, Sales, Inventory Management), with a strong focus on intercompany processes.<br>A central element of this project is building a standardized and replicable implementation model that enables rapid and consistent rollouts to each new subsidiary, supported by local partners in each region. This is not just about implementing D365: it is about designing the way Centogene implements D365.<br><br><span style="font-size:18px;"><br></span><h1><span style="font-size:18px;">Key Responsibilities</span></h1><ul><li>Actively participate in the D365 F&amp;SCM rollout to the group’s international subsidiaries, from requirements analysis through go-live and stabilization.</li><li>Contribute to the design and documentation of a standard implementation model (template) that accelerates successive deployments.</li><li>Configure and parameterize Finance modules (GL, AP, AR) and Supply Chain modules (Procurement, Sales, Inventory), adapting them to each subsidiary’s local requirements.</li><li>Design and configure intercompany flows between the parent company and subsidiaries.</li><li>Create and deliver customizations, extensions, and integrations with local systems as needed.</li><li>Coordinate work with local partners in each region — leading, collaborating, or supervising depending on the project phase.</li><li>Execute data migrations from each subsidiary’s legacy systems.</li><li>Produce technical and functional documentation for the implemented solutions.</li><li>Provide L2 support and training to key users at each subsidiary.</li></ul><br>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<h1><span style="font-size:18px;">What We Are Looking For:</span></h1><br>A professional with hands-on experience in D365 Finance &amp; SCM implementations, combining strong configuration and parameterization skills with sufficient technical knowledge to deliver customizations and integrations. Someone who has participated in multi-entity or multi-country rollouts and is able to contribute to the design of a scalable implementation model.<br><br><h1><span style="font-size:18px;">Essential Requirements</span></h1><ul><li>Proven experience in at least 2 full D365 Finance &amp; Supply Chain Management implementations, preferably in multi-entity or multi-country projects.</li><li>Deep knowledge of Finance modules (GL, AP, AR) and basic Supply Chain (Procurement, Sales, Inventory).</li><li>Hands-on experience configuring intercompany processes.</li><li>Technical ability to deliver customizations and extensions (X++, Power Platform, or integration tools).</li><li>Experience working with or coordinating implementation partners.</li><li>Fluent in English.</li><li>Willingness to travel occasionally to international subsidiaries (kick-offs and go-lives).</li></ul><br><h1><span style="font-size:18px;">Desirable Requirements</span></h1><ul><li>Experience designing replicable implementation models or rollout templates.</li><li>Microsoft certification in D365 Finance or Supply Chain Management.</li><li>Knowledge of Azure and integration tools (Logic Apps, Data Factory).</li><li>Experience in the healthcare, biotech, or pharmaceutical sector.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[Centogene is a global leader in genetic diagnostics and precision medicine, founded in 2006 and headquartered in Rostock, Germany. With presence in over 100 countries, approximately 450 employees across 5 continents, and one of the largest genetic databases in the world, Centogene transforms clinical, genetic, and biochemical data into medical solutions for patients. Recently backed by Charme Capital Partners, the company is undergoing a phase of transformation and global growth.<br><br><h1><span style="font-size:18px;">What We Offer</span></h1><ul><li>Join a strategic, global-scale project at a leading precision medicine company.</li><li>Competitive salary: 60,000 – 90,000€ gross per annum, depending on experience.</li><li>Based in Valencia, Spain, with a hybrid working model.</li><li>Occasional international travel for kick-offs and go-lives.</li><li>The opportunity to design the group’s ERP expansion model from scratch.</li><li>A multicultural and innovative working environment.</li></ul>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>freelance</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>2-5</yearsOfExperience>
    <occupation>desktop_service_and_support</occupation>
    <occupationCategory>it_software</occupationCategory>
    <createdAt>2026-05-18T12:01:30+00:00</createdAt>
    <salaryInformation>
        <min>60000.00</min>
        <max>90000.00</max>
        <currencySymbol>€</currencySymbol>
        <currencyCode>EUR</currencyCode>
        <type>yearly</type>
    </salaryInformation>
</position>

<position>
    <id>2670350</id>
    <subcompany>CENTOGENE Dubai</subcompany>
    <office>United Arab Emirates - Dubai</office>
    <department>Medical Genomics</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Genetic Counselor</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<ul><li>Provide comprehensive pre- and post-test genetic counseling to patients and referring clinicians for diagnostic genetic testing, including PGT-related testing, WES, WGS, NIPT, carrier screening, and targeted gene panels.</li><li>Assess genetic risk by detailed personal and family history evaluation, and explain test indications, limitations, and clinical implications.</li><li>Interpret and communicate complex genetic test results to clinicians and patients in coordination with the laboratory’s medical and scientific team.</li><li>Support informed clinical decision-making by addressing the medical, psychological, and ethical aspects of genetic findings.</li><li>Work closely with molecular geneticists, laboratory technologists, and sales/business development teams to ensure appropriate test utilization and high-quality service delivery.</li><li>Prepare and maintain accurate <strong>clinical documentation and genetic counselling reports </strong>in compliance with laboratory policies and regulatory requirements.</li><li>Participate in case reviews, variant discussions, external clinician support, and continuous professional development activities.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<ul><li>Master’s degree or equivalent diploma in Genetic Counselling<strong> </strong>related field.</li><li>1–2 years of experience in reproductive genetics, rare diseases, or oncology genetics, with exposure to NGS-based testing, carrier screening, PGT, and/or prenatal diagnostics.</li><li>Valid DHA or DOH license (or eligibility) is required.</li><li>Fluency in Arabic and English is mandatory.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[<ul><li>A competitive salary package with additional benefits.</li><li>Opportunities for career development and professional growth within the company.</li><li>A collaborative and innovative work environment.</li><li>The chance to make a significant impact in an innovative company within the healthcare industry.</li></ul>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>1-2</yearsOfExperience>
    <keywords>reproductive genetics,rare diseases,oncology genetics,WES,WGS,NIPT,carrier screening,genetics</keywords>
    <occupation>healthcare_aid</occupation>
    <occupationCategory>medical_and_health</occupationCategory>
    <createdAt>2026-06-12T15:59:16+00:00</createdAt>
</position>

<position>
    <id>2340880</id>
    <subcompany>CENTOGENE Germany GmbH</subcompany>
    <office>Taiwan - Taoyuan City - EUR</office>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Lab Manager – APAC Laboratory</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<ul><li>Lead the setup and establishment of the APAC laboratory in Taoyuan, including equipment installation, workflow design, and process implementation.</li><li>Oversee daily laboratory operations, including equipment maintenance, consumables management, and workflow optimization.</li><li>Conduct and supervise molecular biology experiments (e.g., DNA/RNA extraction, PCR, molecular cloning).</li><li>Hands-on experience with sequencing platforms (e.g., Illumina, Thermo Fisher) including library prep, QC, and data quality assurance.</li><li>Develop and enforce Standard Operating Procedures (SOPs) in compliance with global quality and safety standards (ISO, GLP, CAP).</li><li>Ensure compliance with LDT regulatory requirements in Taiwan and other APAC jurisdictions.</li><li>Train, mentor, and supervise laboratory technicians and junior staff.</li><li>Collaborate effectively with headquarters in Germany and other international teams, including participation in regular meetings and system integration.</li><li>Utilize CENTOGENE’s internal systems for data management, workflow tracking, and reporting.</li><li>Support preparation of scientific reports, project documentation, and publications.</li></ul><br>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<ul><li>Master’s or PhD in Molecular Biology, Biomedical Sciences, Biotechnology, or a related discipline (PhD preferred).</li><li>Solid technical expertise in molecular biology techniques (DNA/RNA extraction, PCR, cloning).</li><li>Hands-on experience with sequencing platforms (e.g., Illumina, Thermo Fisher) including library prep, QC, and data quality assurance.</li><li>Proven experience in laboratory management, ideally with prior involvement in lab setup.</li><li>Strong communication skills in English (spoken and written) for effective interaction with HQ and cross-functional teams.</li></ul>Preferred / Strong Plus:<ul><li>Familiarity with LDT (Laboratory Developed Tests) regulations and compliance requirements.</li><li>Licensed Medical Laboratory Scientist (MT/CLS).</li><li>Experience working under international quality frameworks (ISO, GLP, CAP).</li><li>Previous experience in cross-cultural or multinational environments.</li></ul><br>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[<ul><li>Competitive salary and benefits package.</li><li>Opportunity to lead the establishment of CENTOGENE’s first APAC laboratory.</li><li>Access to state-of-the-art equipment and resources.</li><li>Career growth and professional development in a global biotech leader.</li><li>Close collaboration with international experts and teams.</li></ul><br>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>1-2</yearsOfExperience>
    <occupation>laboratory_and_pathology</occupation>
    <occupationCategory>medical_and_health</occupationCategory>
    <createdAt>2025-09-17T09:41:02+00:00</createdAt>
</position>

<position>
    <id>2533523</id>
    <subcompany>CENTOGENE Japan</subcompany>
    <office>Tokyo - Japan</office>
    <additionalOffices>
        <office>Japan - Tokyo</office>
    </additionalOffices>
    <department>Wet Lab</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Lab Manager – Tokyo Laboratory</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<span style="font-size:14px;">CENTOGENE（セントジェン）は、ドイツのロストックから、希少疾患の患者様の診断を支援するために始まり、今日では希少疾患だけでなくあらゆる臨床専門分野を網羅している世界的なバイオテクノロジー企業です。遺伝学的データ、臨床情報、バイオマーカー（生化学的データ）を統合し、患者・医師・製薬会社の全ての皆様に精密医療（プレシジョン・メディシン）を届けるための検査サービスを提供しています。<br> 今年2026年、日本にも拠点を広げます。東京ラボの開設に伴いラボマネージャーを募集します。ご興味のある方はぜひお問い合わせください。お待ちしております。</span><br><br><span style="font-size:14px;"><strong>Position Summary:</strong></span><br>The Lab Manager (APAC Laboratory) will be responsible for overseeing the setup and daily operations of CENTOGENE’s Japan laboratory. This includes implementing laboratory infrastructure, managing staff, and ensuring compliance with both local and international quality standards.<br> <br>The ideal candidate will have strong expertise in molecular biology and Illumina sequencing, with the ability to lead laboratory operations while collaborating closely with our headquarters in Germany. This position also requires familiarity with LDT (Laboratory Developed Tests) regulatory requirements, to ensure that the laboratory is aligned with both Japanese and international standards.<br><h2><span style="font-family:Arial, Helvetica, sans-serif;font-size:14px;">Key Responsibilities:</span></h2><ul><li>Lead the setup and establishment of the APAC laboratory in Tokyo, including equipment installation, workflow design, and process implementation.</li><li>Oversee daily laboratory operations, including equipment maintenance, consumables management, and workflow optimization.</li><li>Conduct and supervise molecular biology experiments (e.g., DNA/RNA extraction, PCR, molecular cloning).</li><li>Hands-on experience with sequencing platforms (e.g., Illumina, Thermo Fisher) including library prep, QC, and data quality assurance.</li><li>Develop and enforce Standard Operating Procedures (SOPs) in compliance with global quality and safety standards (ISO, GLP, CAP).</li><li>Ensure compliance with LDT regulatory requirements in Japan and other APAC jurisdictions.</li><li>Train, mentor, and supervise laboratory technicians and junior staff.</li><li>Collaborate effectively with headquarters in Germany and other international teams, including participation in regular meetings and system integration.</li><li>Utilize CENTOGENE’s internal systems for data management, workflow tracking, and reporting.</li><li>Support preparation of scientific reports, project documentation, and publications.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<ul><li>Master’s or PhD in Molecular Biology, Biomedical Sciences, Biotechnology, or a related discipline (PhD preferred).</li><li>Solid technical expertise in molecular biology techniques (DNA/RNA extraction, PCR, cloning).</li><li>Hands-on experience with sequencing platforms (e.g., Illumina, Thermo Fisher) including library prep, QC, and data quality assurance.</li><li>Proven experience in laboratory management, ideally with prior involvement in lab setup.</li><li>Strong communication skills in Japanese and English (spoken and written) for effective interaction with HQ and cross-functional teams.</li></ul> <strong>Preferred / Strong Plus:</strong><br><ul><li>- Familiarity with LDT (Laboratory Developed Tests) regulations and compliance requirements.</li><li>- Licensed Medical Laboratory Scientist (MT/CLS).</li><li>- Experience working under international quality frameworks (ISO, GLP, CAP).</li><li>- Previous experience in cross-cultural or multinational environments.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[<ul><li>Competitive salary and benefits package.</li><li>Opportunity to lead the establishment of CENTOGENE’s first Japan laboratory.</li><li>Access to state-of-the-art equipment and resources.</li><li>Career growth and professional development in a global biotech leader.</li><li>Close collaboration with international experts and teams.</li></ul>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>1-2</yearsOfExperience>
    <keywords>#Laboratory Manager,#APAC Laboratory,#Lab Japan,#Lab Tokyo</keywords>
    <occupation>administrative</occupation>
    <occupationCategory>administrative_and_clerical</occupationCategory>
    <createdAt>2026-02-17T13:48:42+00:00</createdAt>
</position>

<position>
    <id>2548498</id>
    <subcompany>CENTOGENE Spain</subcompany>
    <office>Spain - Valencia</office>
    <department>Legal Affairs</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Legal Compliance &amp; Internal Governance Specialist (Valencia)</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<span>Centogene is seeking a <strong>Legal Compliance &amp; Internal Governance Specialist</strong> to strengthen our global legal and compliance framework. This role offers exposure to international operations and cross-border governance matters within a fast-growing life sciences environment.</span><br><br><span><strong>1. Data Protection Compliance</strong><br></span><ul><li>Review and update test requisition forms, informed consent forms, and other data-related documentation.</li><li>Support implementation and monitoring of GDPR and other applicable data protection regulations.</li><li>Coordinate with internal stakeholders to ensure data processing activities align with regulatory requirements.</li></ul><strong>2. Internal Governance</strong><br><ul><li>Support corporate governance matters across multiple jurisdictions.</li><li>Maintain and update records of board members, powers of attorney, and corporate representation systems.</li><li>Coordinate with external counsel on corporate filings and structural changes.</li></ul><strong>3. Intellectual Property &amp; Trademarks</strong><br><ul><li>Support implementation of the global IP and trademark strategy.</li><li>Coordinate trademark applications, renewals, and portfolio management with local external advisors.</li><li>Monitor IP-related risks and ensure internal alignment with corporate policies.</li></ul><strong>4. Legal Database Management</strong><br><ul><li>Maintain and organize the legal documentation database.</li><li>Ensure proper archiving and version control of corporate and contractual documentation.</li><li>Support digitalization and process improvements within the legal function.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<ul><li>2–5 years of professional experience in similar roles, ideally within an international company or a recognized law firm.</li><li>Experience in cross-border corporate governance and compliance matters.</li><li>Solid understanding of data protection regulations (GDPR).</li><li>Exposure to IP and trademark coordination is a plus.</li><li>Strong organizational skills and attention to detail.</li><li>Proactive, structured, and solution-oriented mindset.</li></ul><h3><strong><span style="font-size:15px;">Languages</span></strong></h3><ul><li><strong>Must be able to speak German</strong> (need to communicate with German supervisory authorities, employees, and data subjects, and apply German legislation (GDPR + BDSG).</li><li>Excellent professional and legal English (mandatory).</li><li>Excellent professional and legal Spanish (mandatory).</li></ul><h3><strong><span style="font-size:15px;">What We Offer</span></strong></h3><ul><li>International exposure and interaction with multiple jurisdictions.</li><li>A dynamic and growth-oriented environment within the life sciences sector.</li><li>Opportunity to develop expertise in global governance and compliance matters.</li></ul>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>2-5</yearsOfExperience>
    <occupation>other</occupation>
    <occupationCategory>other</occupationCategory>
    <createdAt>2026-02-27T16:05:22+00:00</createdAt>
</position>

<position>
    <id>2511055</id>
    <subcompany>CENTOGENE Spain</subcompany>
    <office>Spain - Valencia</office>
    <department>Legal Affairs</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Legal Counsel – Corporate &amp; Transactions (International) (Valencia, Spain)</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[We are seeking an experienced <strong>Legal Counsel – Corporate &amp; Transactions</strong> to support the company’s international growth and corporate activities.<br>This role has a strong <strong>international exposure</strong> and will play a key part in the incorporation of new subsidiaries, M&amp;A operations, and the coordination of commercial litigation matters with external advisors across multiple jurisdictions.<br>The position is based in <strong>Valencia (Spain)</strong> and involves close interaction with senior management, external law firms, and internal stakeholders worldwide.<br><br><strong>Key Responsibilities</strong><br><strong>1. Incorporation and Corporate Structuring of New Subsidiaries</strong><br><ul><li>Lead and coordinate the incorporation of new subsidiaries in multiple jurisdictions.</li><li>Liaise with external legal, tax, and notarial advisors to ensure timely and compliant company formations.</li><li>Draft, review, and manage corporate documentation (articles of association, board/shareholder resolutions, powers of attorney, etc.).</li><li>Ensure proper implementation of governance structures in line with group standards.</li><li>Maintain and update corporate records and documentation for international entities.</li></ul><strong>2. M&amp;A Transactions and Post-Closing Integration</strong><br><ul><li>Support M&amp;A operations from a legal and corporate perspective, in close coordination with external law firms.</li><li>Assist in transaction execution, including review of transaction documents, conditions precedent, and closing mechanics.</li><li>Manage post-closing actions such as company name changes, governance updates, appointments and removals of directors, granting/revoking powers, and registry filings.</li><li>Coordinate internal and external stakeholders to ensure smooth post-acquisition integration from a legal standpoint.</li></ul><strong>3. Commercial Litigation and Dispute Coordination</strong><br><ul><li>Act as the internal point of contact for commercial litigation and disputes.</li><li>Coordinate and supervise external legal counsel across different jurisdictions.</li><li>Support the preparation and review of legal strategies, pleadings, and settlement discussions.</li><li>Monitor litigation timelines, risks, and costs, and report regularly to senior management.</li></ul><br><br><br>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<ul><li><strong>Experience:</strong>Minimum of 5 years of relevant experience, either:<ul><li>In the legal department of an international company with strong cross-border activity, or</li><li>In a well-recognized law firm with exposure to corporate, M&amp;A, and commercial litigation matters.</li></ul></li><li><strong>Languages:</strong><ul><li><strong>English:</strong> Very high professional and legal level (written and spoken).</li><li><strong>Spanish:</strong> Very high professional and legal level (written and spoken).</li></ul></li><li>Strong understanding of corporate law, international transactions, and cross-border legal coordination.</li><li>Proven ability to manage multiple projects simultaneously in an international environment.</li><li>Hands-on, pragmatic, and solution-oriented mindset.</li><li>Excellent communication skills and ability to interact with senior stakeholders.</li></ul>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>5-7</yearsOfExperience>
    <occupation>general_and_other_legal</occupation>
    <occupationCategory>legal</occupationCategory>
    <createdAt>2026-01-28T15:44:54+00:00</createdAt>
</position>

<position>
    <id>2390180</id>
    <subcompany>CENTOGENE Germany GmbH</subcompany>
    <office>Taiwan - Taoyuan City - EUR</office>
    <department>Commercial Business</department>
    <recruitingCategory>Regular Employee</recruitingCategory>
    <name>Product Manager (m/f/d) – CentoDx</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<ul><li>Develop and implement product strategies for CentoDx, aligning with CENTOGENE’s global and regional objectives.</li><li>Provide sales enablement and technical training to internal teams, distributors, and clinical partners.</li><li>Conduct product demonstrations, seminars, and workshops for customers and professionals.</li><li>Collaborate with the sales team to identify new opportunities and enhance customer engagement.</li><li>Serve as the product expert, providing scientific and clinical insights for field activities.</li><li>Work with global product and marketing teams on launch planning, content localization, and promotional initiatives.</li><li>Gather market feedback and competitive intelligence to support product improvement.</li><li>Represent the brand at industry events, conferences, and exhibitions.</li></ul>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[Requirements<ul><li>Master’s degree in Life Sciences, Biotechnology, Medicine, or related fields.</li><li>Minimum 6 years of experience in product management, clinical diagnostics, IVD, or life science industries.</li><li>Strong understanding of molecular diagnostics, NGS workflows, and genetic testing.</li><li>Proven experience in delivering product training, demonstrations, and workshops.</li><li>Excellent communication and presentation skills; able to convey technical value clearly.</li><li>Fluent in English and Chinese (Traditional or Simplified); proficiency in other Asian languages is a plus.</li><li>Willingness to travel across the APAC region and work in a cross-functional, international environment.</li></ul>Core Competencies<ul><li>Product Expertise: Deep understanding of molecular diagnostics and clinical applications.</li><li>Training &amp; Communication: Skilled in designing and delivering impactful product education.</li><li>Strategic Thinking: Ability to connect technical capability with business objectives.</li><li>Customer Orientation: Builds trust and value through consultative engagement.</li><li>Cross-Functional Collaboration: Works seamlessly with sales, marketing, and global product teams.</li></ul><br>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[<ul><li>Opportunity to lead the regional growth of a world-class diagnostic solution.</li><li>Competitive salary and performance-based incentives.</li><li>International teamwork and global career development.</li><li>A science-driven, collaborative, and inclusive company culture.</li></ul>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>experienced</seniority>
    <schedule>full-time</schedule>
    <yearsOfExperience>5-7</yearsOfExperience>
    <keywords>Product Manager,CentoDx,Molecular Diagnostics,Genetic Testing,IVD,MolecularDiagnostics,Healthcare,APACJobs,CENTOGENE</keywords>
    <occupation>general_and_other_medical_and_health</occupation>
    <occupationCategory>medical_and_health</occupationCategory>
    <createdAt>2025-10-15T12:57:58+00:00</createdAt>
</position>

<position>
    <id>2641775</id>
    <subcompany>CENTOGENE Germany GmbH</subcompany>
    <office>Germany - Rostock</office>
    <department>Quality and Regulatory</department>
    <name>Quality Manger (Rostock)</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[<p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">Your core responsibilities will include, but are not limited to:</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">· Support continuous improvement and maintenance of the QMS in compliance with:</span></p><ul style="list-style-type:disc;"><li><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">ISO 13485</span></p></li><li><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">ISO 15189</span></p></li><li><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">Global regulatory requirements (e.g., MDSAP)</span></p></li></ul><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">· Ensure compliance with international quality standards and regulatory requirements</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">· Participation in regulatory inspections and external audits; support the planning and execution of internal audits</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">· Manage and oversee:</span></p><ul><li><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">Change control processes</span></p></li><li><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">Non-conformities (NCs)</span></p></li><li><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">CAPA processes</span></p></li><li><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">SCARs</span></p></li></ul><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">· Support with document control activities, including updates and maintenance in the eDMS</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">· Perform Quality Control activities</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="color:rgb(0,0,0);font-family:Arial, Helvetica, sans-serif;">· Contribute to risk assessment processes</span></p>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[<p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">Education:</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Degree in life sciences or a related scientific discipline</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Additional qualification in Quality Management is considered a plus</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">Knowledge and Skills:</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Background in the life sciences sector; experience in the biotechnology or pharmaceutical industry will be highly valued</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Proven experience with of ISO 15189, ISO 13485 and ISO14971 standards</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Knowledge of MDR, IVDR, FDA QMSR</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· CLIA, CAP and GMP awareness is a plus</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Strong understanding of quality methods and problem-solving tools (e.g., FMEA, 5 Whys, Ishikawa)</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Strong analytical, structured, and solution-oriented working style</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Strong communication skills and confidence working with cross-functional teams</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Ability to work in a structured, detail-oriented and compliant manner</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Proficiency in Microsoft Word, Excel and electronic document management systems (eDMS)</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Fluent in English (written and spoken)</span></p>]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[<p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">What we offer</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Exciting International and diverse team which stands for integrity, involvement and innovation within the life sciences sector</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Training &amp; development opportunities</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Company benefits such as company health insurance and company discounts</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Primarily on-site role with some remote work flexibility</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">· Permanent contract</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;"><br></span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">About us</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">With employees from over 50 nations, CENTOGENE is a truly international company with offices is in Rostock, Berlin, Delhi, Boston, Valencia, Belgrade, and São Paulo. We were born to help diagnostic patients with rare disease and today we evolved to help patients of all clinical specialties to make bold progress with guided solutions for physicians, their patients and pharma partners.</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">Our Values</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">We Care: A culture of empathy and understanding for each other, our customers, and our patients, constantly driving our mission forward</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">We Innovate: A culture of big ideas, being bold, and taking calculated risks to develop never-before-seen solutions</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">We Act With Integrity: A culture of keeping to our principles with self-awareness, intellectual honesty, and speaking up</span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;"><br></span></p><p style="color:rgb(0,0,0);font-family:'Times New Roman';font-size:medium;font-style:normal;font-weight:400;text-transform:none;"><span style="font-family:Arial, Helvetica, sans-serif;">If you are interested, we look forward to receiving your application, including your CV, motivation letter, earliest possible start date, and salary expectations.</span></p>]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>permanent</employmentType>
    <seniority>entry-level</seniority>
    <schedule>full-time</schedule>
    <keywords>#Quality #Manger</keywords>
    <occupation>general_and_other_quality_assurance_and_safety</occupation>
    <occupationCategory>quality_assurance_and_saftey</occupationCategory>
    <createdAt>2026-05-19T17:20:33+00:00</createdAt>
</position>

<position>
    <id>2624545</id>
    <subcompany>CENTOGENE Germany GmbH</subcompany>
    <office>Germany - Rostock</office>
    <department>Finance</department>
    <recruitingCategory>Werkstudenten</recruitingCategory>
    <name>Working Student Accounts Receivable (m/f/d)</name>
    <jobDescriptions>
        <jobDescription>
            <name>Your Responsibilities</name>
            <value>
                <![CDATA[• Assisting with accounts receivable<br>• Processing and posting outgoing invoices<br>• Assisting with mail processing and master data maintenance<br>• Assisting with month-end closing]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Your profile</name>
            <value>
                <![CDATA[• Enrolled in an economics program or a comparable degree program<br>• Proficient in MS Office applications<br>• Good time management and flexibility<br>• Available for 15 to 20 hours per week<br>• Accounting knowledge or completion of training as a tax clerk are an advantage but not a requirement<br>• Good English skills are desirable]]>
            </value>
        </jobDescription>
        <jobDescription>
            <name>Why us?</name>
            <value>
                <![CDATA[• Regular company events and a free fitness area with a view of the city<br>• We support our employees individually through internal and external training<br>• Hourly wage of at least €14]]>
            </value>
        </jobDescription>
    </jobDescriptions>
    <employmentType>working_student</employmentType>
    <seniority>student</seniority>
    <schedule>part-time</schedule>
    <yearsOfExperience>lt-1</yearsOfExperience>
    <keywords>#finance,#receivable</keywords>
    <occupation>accounts_payable_and_receivable</occupation>
    <occupationCategory>accounting_and_finance</occupationCategory>
    <createdAt>2026-05-05T14:20:20+00:00</createdAt>
</position>

</workzag-jobs>