Jobs at futureproof

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 end-to-end rollout of enterprise digital solutions across the UK and Ireland within a pharmaceutical fertility business. Coordinate global product teams, local stakeholders, vendors, IT, and business functions; manage implementation plans, integrations, data migration, UAT, training, governance, risks, and hypercare. Drive change management, business readiness, user adoption, KPI tracking, regulatory compliance, and senior leadership reporting across multinational projects.

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.

Develop and maintain a cloud-native clinical data platform using Python, AWS, React, and TypeScript. Build data transformation pipelines, Lambda services, Step Functions workflows, GraphQL APIs, event-driven systems, infrastructure automation, and large-scale Databricks processing. Troubleshoot production issues, improve CI/CD, participate in architecture decisions, conduct code reviews, and mentor junior engineers. The platform transforms clinical trial data into CDISC SDTM standards supporting regulatory submissions and pharmaceutical research.

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.

Design, implement, and support secure, scalable data movement and storage services across enterprise infrastructure and AWS. Administer SMB/CIFS and NFS storage, manage Amazon S3 configurations, troubleshoot performance and connectivity issues, and automate operations using Python, Bash, or PowerShell. Collaborate with infrastructure, cloud, networking, and application teams to maintain highly available services. Preferred experience includes AWS storage services, enterprise NAS platforms, infrastructure-as-code tools, and regulated environments.

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.

Design, build, and maintain scalable AWS data pipelines and platforms using Python, SQL, Spark, PySpark, Databricks, and Dataiku. Develop ETL/ELT workflows, optimize Redshift and S3 solutions, automate infrastructure with Terraform and CloudFormation, and maintain CI/CD pipelines. Monitor and troubleshoot data workloads, document solutions, and collaborate with global stakeholders. The role supports regulated clinical, laboratory, scientific, and pharmaceutical data environments.

Design, develop, and maintain secure, scalable AWS infrastructure using Terraform and reusable HCL modules. Build CI/CD pipelines, develop Lambda functions with Node.js and TypeScript, manage AWS networking and edge services, and ensure security, compliance, observability, reliability, and cost efficiency. Troubleshoot production issues, optimize cloud environments, and participate in on-call production support.

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.

Design, build, and maintain scalable Python and Databricks ETL/ELT pipelines across data lakes and warehouses. Develop data models, quality checks, monitoring, orchestration, catalogs, and lineage practices. Collaborate with analysts, data scientists, and ML engineers to improve data accessibility and reliability. Apply testing, Git workflows, Docker, CI/CD, and SDLC documentation in a remote, regulated enterprise environment.

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.

Configure, document, test, integrate, deploy, and support Benchling scientific workflows for protein engineering and microbial infrastructure. Translate scientific and business requirements into scalable configurations, integrations, data mappings, interface specifications, and technical designs. Support APIs, event-driven integrations, SIT, UAT, defect resolution, deployment, hypercare, user onboarding, training, and post-implementation operations while collaborating with scientists, stakeholders, enterprise technology teams, and Benchling Professional Services.