Jobs at Vantive

Lead design and delivery of API-driven enterprise integration solutions using MuleSoft and cloud technologies. Provide technical leadership across EAI projects, collaborate with product and architecture teams, create reusable integration patterns, troubleshoot and resolve integration issues, and guide junior engineers to ensure scalable, secure implementations aligned with enterprise architecture.

Lead academic promotion of company products within an assigned region, execute regional marketing activities and projects, maintain brand image, visit and develop relationships with clients, monitor market dynamics, and report feedback to management.

Lead global sterilization strategy and validation for medical devices and related solutions. Develop and qualify sterilization cycles (radiation, EO, VHP, moist heat), run sterility assurance studies, analyze data, support regulatory interactions, troubleshoot processes, and guide cross-functional teams. Serve as subject-matter expert, produce technical reports, and ensure compliance with GMP and relevant sterilization regulations.

Lead regional academic promotion for peritoneal dialysis products: execute academic strategies, communicate clinical/drug information to healthcare institutions, collect clinical and market feedback, ensure regulatory and company compliance, complete representative filings, and support optimization of promotion plans.

Lead strategy and execution for the Chronic PD portfolio across Central/North Florida. Grow PD referrals and market share through physician and business relationships, negotiate and manage local contracts, align resources with PD Clinical Specialists, maintain territory sales funnel in Salesforce, and travel frequently to meet territory forecasts and close new business.

Perform routine microbiological testing, environmental monitoring, and sterilization validation per SOPs. Report abnormalities and assist investigations, perform basic equipment maintenance, follow lab safety practices, dispose of biohazard materials, and ensure compliance with EHS policies.

Lead delivery and operations for Commercial Sales & Marketing IT, managing internal teams and external vendors to design, deliver, and optimize sales, marketing, and service applications. Own solution architecture, budget, vendor relationships, and application rationalization while aligning with enterprise platforms, regulatory requirements, and product owners to enable business growth and differentiation.

Support and coordinate digital transformation projects for Latin America North using agile frameworks. Facilitate multidisciplinary teams, monitor progress, risks, budgets, and metrics; coach agile practices; translate clinical/regulatory needs into technical deliverables; and drive implementation of clinical apps, telemedicine, remote monitoring, and analytics.

Lead employee relations, training, and manpower management for a manufacturing site. Ensure policy compliance, conduct investigations and exit interviews, run engagement and recognition programs, design and deliver training and induction, manage training budgets and HRIS records, coordinate hiring and contingent labor, and support contractor and welfare administration.

Designs and implements stability strategies and GMP studies for new and existing drug products, analyzes stability data, authors regulatory stability sections, oversees multiple stability projects (including CRO interactions), acts as study director, ensures appropriate methods/specifications, participates in investigations, and coaches junior staff while maintaining cGxP and regulatory compliance.

Support supply chain strategy by building ETL and visualization tools, performing statistical and predictive modeling, conducting ad-hoc analyses, developing KPIs, and partnering cross-functionally to optimize supply chain efficiency, reduce costs, and enable data-driven decisions.

Lead end-to-end DevOps support for regulated medical device software: implement monitoring, resolve incidents within SLAs, drive root-cause analysis, develop SOPs, collaborate with global stakeholders and ensure high-availability operations.

Lead strategic messaging, positioning, and value communication for Vantive's digital products and services. Develop messaging frameworks, conduct customer and competitive insight, partner with cross-functional and regional teams to localize activations, support marketing assets and launches, and monitor regulatory and market trends to ensure cohesive global storytelling and go-to-market alignment.

Lead territory commercial strategy and execution to meet sales objectives. Build and negotiate with key clients, manage contracts and tenders, coordinate with Medical Affairs and Market Access, track KPIs and sales commitments, and develop and retain team talent while implementing corporate tools and service-level agreements.

Provide technical maintenance support for manufacturing equipment: inspect, troubleshoot, repair, perform reactive and preventive maintenance, document procedures, support continuous improvement, and collaborate with production and maintenance teams to ensure operational efficiency and uptime.

Lead systems engineering for medical device products across the lifecycle: manage requirements, traceability, DHF, product risk, integration, verification and validation. Drive system-level design, influence cross-functional teams, mentor engineers, ensure compliance with FDA/ISO/IEC standards, perform impact assessments and mitigation strategies, and lead technical feasibility and reliability activities for acute therapy devices.

Design, build, and maintain scalable internal platforms using IaC, automation, and CI/CD. Develop Terraform and CloudFormation templates, Python and shell automation, implement policy-as-code and guardrails, onboard application teams, monitor platform reliability, and document best practices to improve security, scalability, and developer productivity.

The posting contains no listed responsibilities or qualifications. The title indicates a Senior Clinical Coordinator role, typically involving coordination of clinical activities and support for clinical operations.

Lead and mentor an engineering team to design, develop, and implement automated manufacturing equipment, drive process improvements, manage multiple projects and budgets, coordinate stakeholders and contractors, and ensure safety, quality, cost, and efficiency in a regulated medical/pharma environment.

Lead and support site EHS programs across Castlebar and Swinford: ensure regulatory compliance, manage hazardous waste, conduct inspections and audits, perform risk assessments and incident investigations, drive corrective actions, maintain EHS KPIs, and promote continuous safety improvements.