Jobs at Vantive

Leads analysis, configuration, implementation, upgrades, and support for JD Edwards EnterpriseOne supply chain modules. The role supports procurement, warehousing, inventory, transportation, quality, sales order management, EDI, and WMS integrations. Responsibilities include translating business requirements into solutions, troubleshooting integrations, supporting FDA-compliant validation and audit readiness, cloning applications for a new technology landscape, coordinating third-party teams, training users, and driving continuous improvement.

Lead analysis, configuration, implementation, upgrade, and support of JD Edwards EnterpriseOne supply chain modules. Translate business requirements into functional solutions, troubleshoot integrations, support WMS and EDI processes, ensure FDA and medical-device compliance, and help clone applications into Vantive’s standalone technology environment. The role also includes stakeholder collaboration, third-party vendor coordination, end-user training, documentation, continuous improvement, and global ERP support.

Lead financial reporting, forecasting, annual planning, variance analysis, dashboards, and scenario modeling for assigned manufacturing business areas. Partner with plant and operations leadership on inventory, costs, productivity, capital expenditures, and improvement initiatives. Support internal controls, audits, inventory valuation, standard cost reviews, and trade compliance submissions while providing actionable financial insights.

Promotes company products academically within an assigned region, executes regional marketing activities, maintains brand image, develops customer relationships, monitors market trends, and reports feedback. Requires a medical, pharmaceutical, or related degree, at least three years of pharmaceutical industry experience, clinical promotion expertise, commercial awareness, communication skills, teamwork, integrity, and strong results orientation.

Lead regulatory strategy and execution for complex drug manufacturing and import projects. Represent cross-functional teams, ensure alignment with regulatory requirements, monitor regulations and perform gap analyses, engage health authorities, shape external guidelines, and manage regulatory intelligence and stakeholder relationships to deliver on-time, high-quality regulatory outcomes.

Execute day-to-day master data operations across item, supplier, customer, finance, and other domains. Investigate incidents, resolve work requests, maintain data quality, perform root cause analysis, monitor SLAs, and support governance and compliance activities. Partner with business stakeholders and technical teams, develop reporting and KPIs, support testing and data migrations, document processes, and contribute to MDM projects and continuous improvement initiatives.

Supports pharmaceutical and medical device quality assurance and regulatory compliance in Korea. Responsibilities include product release, labeling, analytical method transfers, field actions, complaint handling, post-market reporting, quality documentation, licensing, audits, change controls, training compliance, warehouse quality, third-party oversight, and GMP/GWP improvements. The role collaborates with Regulatory Affairs and cross-functional teams and requires a Korean pharmacist license, pharmaceutical QA experience, and knowledge of Korean regulations.

Prepare statutory financial statements and tax filings, coordinate external audits, manage tax accounting and compliance, support month-end close, perform reconciliations in BlackLine, maintain SOX controls, and drive finance process improvements. The role partners with finance teams, auditors, tax advisors, and authorities while mentoring junior staff and supporting regional and global finance projects.

Leads APAC MES and global SCADA strategy, delivery, operations, compliance, and continuous improvement. Manages a distributed team, manufacturing IT roadmap, vendors, resources, governance, risks, and stakeholder relationships. Partners with manufacturing, quality, engineering, automation, site leadership, and global IT teams to deliver reliable, validated, and scalable systems. Requires strong technical project management, MES and SCADA knowledge, people leadership, and experience supporting regulated manufacturing environments.

Lead APAC strategic commercial transformation projects through PMO governance, workstream coordination, executive reporting, change management, communications, risk management, organizational design, and benefits realization. The role partners with senior stakeholders across supply chain and related functions to improve operational and commercial outcomes, establish consistent transformation practices, and support adoption across regional teams.

Lead APAC strategic commercial transformation projects across Supply Chain and related functions. Establish PMO governance, coordinate workstreams, manage risks and dependencies, prepare executive reporting, lead change management and communications, support organisational design, facilitate stakeholder governance, and track measurable benefits realization across regional initiatives.

Supports manufacturing engineering projects involving process improvement, production and quality data analysis, Lean Manufacturing, equipment validation, process qualification, documentation, production trials, and equipment evaluations. Collaborates with Operations, Quality, Maintenance, and Supply Chain teams in a regulated medical device manufacturing environment while following safety and regulatory requirements.

Technical lead for global supply chain planning applications (Kinaxis RapidResponse). Own system design, configuration, validation, testing, upgrades, and issue resolution. Gather requirements, architect solutions, manage change control, ensure regulatory compliance (CSV/GxP), and act as primary liaison with IT, business owners, and vendors.

Leads verification and validation testing for electrical and mechanical medical device components and systems. Develops test plans, protocols, methods, fixtures, acceptance criteria, schedules, and reports; performs functional, feasibility, characterization, and pre-compliance testing; analyzes requirements and traceability; troubleshoots failures; and collaborates with R&D, quality, regulatory, manufacturing, and project teams.

Develop and execute provider-focused digital marketing strategies, growth initiatives, communication plans, and product or service launch programs for large dialysis organizations. Lead cross-functional planning, marketing execution, content development, promotional materials, webinars, website content, and digital campaigns. Track KPIs and customer success metrics, optimize engagement through analytics, represent the digital function with key customers, and collaborate across sales, clinical, product, creative, and global marketing teams.

Leads systems engineering for acute therapy medical devices across the product lifecycle. Owns requirements management, traceability, risk and reliability activities, system integration, verification and validation, design history files, change control, and regulatory compliance. Coordinates cross-functional teams, schedules, resources, and product integration activities while translating clinical, user, regulatory, and manufacturing needs into product designs. Presents project status to leadership and supports FDA, ISO, and IEC design control requirements.

Leads the plant’s margin improvement, operational excellence, and strategic initiative portfolio. Owns opportunity pipelines, governance, cross-functional execution, business cases, savings validation, ROI analysis, and benefit sustainment. Partners with Finance and operational stakeholders to deliver measurable improvements in cost, productivity, service, quality, and efficiency while managing risks, milestones, escalations, and executive updates.

Lead E&L and trace analysis for medical devices and drug products using LCMS/GCMS/HRMS. Design and execute studies, perform structural elucidation and unknown identification, supervise CRO work, author regulatory reports, and support change control with cross-functional teams to ensure compliance and product safety.

Leads end-to-end incentive compensation operations, including plan administration, calculations, validation, payouts, quota deployment, reporting, and governance. Owns compensation platforms, system enhancements, automation, data integrity, and process optimization. Delivers analytics, dashboards, modeling, and executive insights while partnering with Finance, HR, IT, vendors, and commercial leadership. Supports territory design, organizational changes, integrations, and change management, serving as a subject matter expert and cross-functional advisor.

Leads finance application capabilities for intercompany, costing, transfer pricing, and controls within JDE. Provides functional design, testing governance, L2 support, audit readiness, SOX and segregation-of-duties oversight, documentation, knowledge transfer, and issue resolution. Partners with Finance, IT, Data, Audit, and managed services teams to stabilize close-critical operations, standardize controls, improve data quality, and support transformation initiatives.