Jobs at futureproof

Lead enterprise platform integration strategy by establishing standardized API governance, reusable integration patterns, and scalable data-flow architectures. Architect reliable connections between SaaS platforms, identity systems, data layers, and business consumers. Translate business needs into practical technical designs, guide implementation, establish resilience and performance standards, and align engineering teams with stakeholders across a matrixed organization.

Owns enterprise ServiceNow Change and Release Management governance in a regulated GxP environment. Responsibilities include assessing change risks, verifying CSV evidence, coordinating multi-workstream release schedules, leading CAB meetings, representing platform governance to executives, and enforcing ITIL-aligned Change, Release, Incident, and Problem Management processes.

Designs and governs enterprise Power BI architecture, including semantic models, datasets, reports, security, workspaces, deployment, CI/CD, and lifecycle standards. Develops advanced DAX and Power Query solutions, optimizes performance and refresh processes, and integrates enterprise data sources using SQL. Provides architectural guidance, governance, technical reviews, and stakeholder collaboration within a global, regulated pharmaceutical environment.

Deliver CRM and EMR implementations across Nordic fertility clinics by gathering requirements, configuring systems, coordinating testing and data migration, supporting training and change management, and providing post-go-live support. The role works with clinic teams and central business functions to align stakeholders, resolve issues, ensure compliance, and improve clinical and administrative processes.

Own and evolve data products supporting pharmaceutical Development Sciences and Clinical Supply. Gather requirements, define business rules, create logical data models, mappings, schemas, metadata, and lineage, and support data lifecycle management. Analyze laboratory and scientific data from LIMS, Signals, and related platforms while collaborating with scientists, engineers, architects, QA, and product teams. Support Agile delivery, UAT, documentation, data quality, governance, and GxP compliance.

Lead enterprise OT cybersecurity architecture for regulated manufacturing environments. Define security standards, reference architectures, governance frameworks, network segmentation, secure IT/OT and cloud connectivity, identity and access controls, vulnerability management, and incident response requirements. Apply IEC 62443, NIST SP 800-82, the Purdue Model, industrial DMZ architectures, and defense-in-depth principles. Facilitate cross-functional workshops, technical reviews, governance forums, and standards approval across IT, OT, engineering, manufacturing, quality, and cybersecurity teams.

Lead global enterprise systems rollout programs across multiple regions, owning implementation strategy, roadmaps, deployment waves, governance, risks, budgets, KPIs, and milestones. Manage and mentor Rollout Managers while coordinating Product, IT, business, and regional teams. Ensure consistent delivery quality, stakeholder alignment, adoption, and continuous improvement across international implementations.

Lead computer system validation and compliance activities for computerized manufacturing and laboratory systems in regulated pharmaceutical environments. Develop, review, and approve lifecycle documentation; assess risks; guide CSV/CSA, qualification, change control, CAPA, deviations, data integrity, and system lifecycle compliance. Collaborate with Quality, Engineering, Automation, IT/OT, laboratory, and business teams. Support audits, inspections, remediation, and capital projects while ensuring adherence to GxP, GMP, FDA, EMA, and international expectations.

Lead industrial automation and digital projects across multiple Irish pharmaceutical manufacturing sites. Manage scope, budgets, schedules, risks, resources, vendors, stakeholders, client relationships, and portfolio performance. Ensure compliance with GxP, CSV, SDLC, and change-control requirements. Coordinate delivery teams, support business development, partner with product and architecture teams, and coach internal staff. Requires extensive IT/OT, DeltaV, regulated manufacturing, and project management experience, with travel to sites approximately four days weekly.

Supports Agilent OpenLAB CDS across pharmaceutical laboratories by gathering requirements, analyzing workflows, configuring system functions, coordinating integrations, supporting GxP validation and UAT, managing defects, reviewing releases, maintaining governance documentation, and training users. Acts as the liaison among scientists, Quality, IT, and integration teams while providing functional support and ensuring audit readiness.

Leads client-facing delivery of enterprise Informatica IDMC solutions, including architecture, development, data integration, data quality, governance, cataloging, and PowerCenter modernization. Coordinates onsite stakeholders with offshore teams, manages requirements, project planning, risks, resources, Agile delivery, testing, deployment, and post-production support. Designs ETL/ELT integrations across cloud platforms, SAP S/4HANA, and enterprise applications while ensuring scalability, security, compliance, and quality.

Leads computer system validation and compliance for computerized manufacturing and laboratory systems in a GMP pharmaceutical environment. Oversees validation lifecycle documentation, risk assessments, qualification, change controls, deviations, CAPA, data integrity, audits, and regulatory inspections. Advises cross-functional Quality, Engineering, Automation, IT, Manufacturing, and Laboratory teams while tracking project deliverables and compliance milestones. Requires experience with platforms such as DeltaV, Rockwell or Siemens PLCs, process historians, or laboratory automation systems, with onsite work twice weekly in West Point, Pennsylvania.

Design and implement secure, scalable AWS architectures while leading DevOps strategy, Infrastructure as Code, CI/CD, Kubernetes, and Amazon EKS operations. Build resilient cloud environments, automate deployments, establish observability and incident response, optimize performance and cost, troubleshoot complex infrastructure issues, and provide technical leadership across engineering, security, architecture, and operations teams.

Design and implement data models and complex dbt/SQL transformations for migrating and consolidating enterprise and laboratory data into an AWS platform. Query distributed sources with Trino/Presto, integrate systems such as SAP, GLIMS, and Veeva, validate data quality, optimize pipelines, and maintain lineage and documentation. Collaborate with architects, analysts, engineers, and pharmaceutical stakeholders in an Agile environment, supporting testing, code reviews, and CI/CD.

Supports adoption, configuration, validation, documentation, testing, release management, and continuous improvement of laboratory instrument data acquisition software in pharmaceutical R&D. Acts as a liaison among laboratory, business, quality, and IT teams; gathers requirements, manages onboarding and integrations, develops UAT and regression testing, supports users, prepares training materials, and ensures GxP and non-GxP compliance.

Owns enterprise-wide standardization and governance of industrial automation products across global manufacturing sites. Responsibilities include managing product footprints, metadata, taxonomies, lifecycle information, requirements, documentation, and data semantics. The role partners with Product Management, Engineering, IT/OT, Manufacturing, and OEM vendors; builds governance processes; maintains Confluence and SharePoint knowledge repositories; and promotes reusable standards and communities of practice.

Supports the design, deployment, validation, and operational management of laboratory instrument data acquisition platforms in pharmaceutical R&D environments. Configures hybrid on-premises and AWS infrastructure, troubleshoots instrument and software connectivity, manages releases, creates IQ/OQ and SDLC documentation, supports UAT, and coordinates global deployments. The role also provides technical support, user training, stakeholder communication, and leadership for small technical teams while ensuring GxP compliance.

Leads CSV, quality compliance, and validation activities for computerized manufacturing and automation systems in a GMP-regulated pharmaceutical environment. Manages project governance, timelines, risks, resources, documentation, deviations, CAPA, change control, and compliance milestones. Coordinates cross-functional teams across Quality, Validation, Engineering, Automation, IT, and Business functions while providing stakeholder updates and guiding teams on GxP, CSA, SDLC, qualification, data integrity, and risk-based validation.