• Manage the supplier change notification lifecycle, including evaluation, risk assessment, approval, tracking, and closure. • Perform trend analysis of supplier quality data and proactively identify emerging risks. • Review, analyze, and report supplier trends, including effectiveness and sustainability of corrective actions. • Interface and collaborate with Supply Chain, Incoming Quality, Quality Assurance, Technical Services, Manufacturing, and other stakeholders to resolve supplier quality issues. • Identify, document, and close gaps between Supplier Quality practices and corporate and local procedures, ensuring regulatory and procedural compliance. • Guide and mentor peers in the application of statistically based quality engineering methodologies, including data analysis, interpretation of results, and risk-based decision making. • Assess existing supplier quality processes and recommend improvements to enhance compliance, efficiency, and robustness. • Support supplier qualification, performance monitoring, and ongoing quality development activities, including on-site and remote engagements. • Participate in supplier audits, quality reviews, and business reviews as required. • Ensure supplier quality activities comply with cGMP, global pharmacopoeias, and international regulatory expectations. • Prepare and maintain clear, concise, and compliant documentation, metrics, and reports for internal and external stakeholders.

• Collaborate with the sales team to secure and expand business with new and existing end-user customers, Cloud, and Hosting Providers. • Conduct web-based and on-site demonstrations of the Veeam product portfolio, providing training, enablement, and participating in joint meetings. • Offer pre-sales support and on-site assistance to customers during their evaluation of Veeam software. • Build and maintain strong relationships with customers and strategic alliance partners in coordination with sales colleagues. • Contribute to and participate in Veeam marketing events. • Conduct Product Proof of Concepts (POCs) for customers. • Prepare Bills of Materials (B.O.M), RFPs/RFQs based on customer needs. • Demonstrate new technologies and provide training to internal staff and customers. • Independently identify and qualify business opportunities. • Provide technical compliance and competitive analysis of products within the solution. • Possess hands-on experience in Hypervisors and Cloud environments. • Coordinate presales efforts with customers, working with Veeam Solution Architects, System Integrators, and Professional Services figures.

• Analyze requirements and participate in clarifying tasks before development starts • Identify ambiguities, risks, and formulate questions about the product • Perform manual testing (frontend / backend) of new features and changes • Write and maintain automated tests (TypeScript + Playwright) • Verify edge cases, negative and regression scenarios • Work with logs (Kibana) to search for and analyze errors • Validate data in databases (SQL / NoSQL) • Update test cases when functionality changes • Expand the regression test suite • Create and maintain test documentation • Participate in improving testing processes

Title: Sr. Vendor Auditor (Auditor III/Compliance Manager) - Remote, United Kingdom - Remote, Romania - Remote, Serbia - Remote, Czechia - Remote, Bulgaria - Remote, Poland - Remote, Hungary Full time   Join us as a Sr. Auditor (Auditor III/ Compliance Manager) on the Vendor and Information System Audits Team and make an Impact at the Forefront of Innovation!   Position overview: The Sr. Auditor is responsible for conducting complex external (vendor) GxP audits to ensure compliance with established quality assurance processes, standards, global regulatory guidelines (e.g., EMA, MHRA, FDA), and client contractual obligations. The Sr. Auditor also identifies issues impacting the quality and/or integrity of clinical research programs, determining adequacy of the root cause of non-conformance and the actions to address issues. What You'll Do: - Lead and report a variety of GMP, GLP and GCP qualification and routine vendor audits, as requested by senior management, including but not limited to on-site, virtual and remote audits of service providers used in clinical trials with or without technology components - Perform directed vendor audits - Provide GxP and QA consultation and support to internal and external clients - Prepare and present audit findings and/or other related information at departmental, internal operations or client meetings - Mentor junior staff. - Lead process/quality improvement initiatives. - Develop tools and other materials for tracking of compliance management activities and analyze trends. Required Education & Experience: - Bachelor's degree or equivalent and relevant formal academic / vocational qualification - Previous QA and GxP vendor auditing experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years). - Fluency in English   Required Knowledge, Skills & Abilities: - Solid knowledge of the clinical trial process - Thorough knowledge of GxP and appropriate regional research regulations and guidelines - Demonstrated proficiency leading a wide range of GxP vendor audits to high standards - Excellent oral and written communication skills (including appropriate use of medical and scientific terminology) - Proven training/mentoring experience of staff - Strong attention to detail - Effectively works independently or in a team environment - Highly developed problem solving, risk assessment and impact analysis abilities - Solid experience in root cause analysis and CAPA development - Expert knowledge of procedural document development - Strong negotiation and conflict management skills - Proven adaptability - Strong organizational and time management skills including flexibility and ability to multi-task and prioritize competing demands/workload - Strong computer skills; ability to learn and become proficient in appropriate systems - Valid driver's license and ability to qualify for and maintain a corporate credit card with sufficient credit line for business travel   The following is a plus: - Experience performing other types of QA audits or activities (e.g., investigator site audits, process audits, database audits, clinical study report audits, process improvement) - Experience hosting client audits and/or regulatory inspections.