• This Warehouse Automation Engineering position can be responsible for he effort in identifying, evaluating, piloting and deploying new warehouse automation technologies • Work directly with internal operations, solution design, continuous improvement, information technology, product teams and stakeholders to identify, select, and deploy new technology with automation partners • Consult with internal and external contacts to quickly demonstrate the value and feasibility of warehouse automation capabilities to create a competitive differentiator • Build ROI and justification based upon multiple criteria in order to select the optimal solution design • Support automation project lead on identifying gaps in vendor FSD/SOW using the FSD Checklist process • Provide input on automation solution designs to ensure that key items are considered for implementation and ongoing operational performance • Help lead build collateral for vendor tech review request and requests for quotes • Some Project Management of smaller projects, including updating of Punch List, Project Plan • Verify and prioritize optimal on-stie support is utilized on all projects • Support on-site Solution Acceptance Test (SAT) testing plan

• Design, develop, test, and deploy RPA processes using the Blue Prism platform, adhering to best practices and coding standards. • Use Claude to analyze existing BluePrism "Code Stages" (.NET/C#) and legacy SQL procedures. • You will be responsible for identifying technical debt and refactoring code for 2x performance gains. • Develop and integrate Python scripts and modules within Blue Prism processes for complex logic, data manipulation, API interactions, and advanced functionalities not natively supported by Blue Prism. • Collaborate with Business Analysts and Solution Architects to understand process requirements (PDDs, SDDs) and translate them into efficient and scalable automation designs. • Use AI to generate complex, synthetic test data and identify "unhappy path" scenarios that traditional unit testing often misses, ensuring 100% production readiness. • Utilize LLMs to ingest system logs and error reports during L3/L4 escalations to accelerate Root Cause Analysis (RCA) and suggest permanent architectural fixes. • Provide ongoing support, monitoring, and maintenance for deployed RPA solutions, including debugging, patching, and performance tuning. • Deep understanding of Multi-VM scalability and memory management to prevent production crashes. • Communicate progress, challenges, and blockers clearly and proactively to team leads and project managers. • Collaborate closely with business stakeholders, process analysts, and engineering teams using agile delivery practices.

Role Description This role is responsible for ensuring the integrity, compliance, and continuous improvement of global quality systems within a regulated environment. The Global Quality Systems Manager maintains oversight of key quality processes, monitors performance metrics, and drives corrective and preventive actions to enhance system effectiveness. This position partners with cross-functional teams worldwide to strengthen compliance, optimize workflows, and support business objectives. The manager provides strategic guidance on audits, regulatory readiness, and quality documentation while ensuring alignment with ISO 13485 standards. Success requires analytical rigor, strong organizational and communication skills, and the ability to influence teams across multiple geographies. The role includes up to 25% travel, both domestic and international, to support audits, inspections, and collaborative projects. - Maintain, monitor, and improve quality system processes, including nonconformance management, logistics complaints, CAPA, internal audits, and planned deviations. - Review and approve quality records, ensuring accuracy, completeness, and regulatory alignment; escalate systemic issues and drive corrective actions. - Analyze quality performance metrics, present insights to leadership, and ensure actionable follow-up during management reviews and business meetings. - Oversee preparation and documentation of Management Review outputs, ensuring decisions and action items are clearly communicated. - Manage the annual internal audit program, including planning, execution, and verification of corrective actions. - Ensure ongoing compliance with ISO 13485 and other applicable regulations, leading readiness activities for external inspections or audits. - Partner with global cross-functional teams to drive compliance and continuous improvement initiatives, enhancing quality system maturity and culture. Qualifications - Bachelor’s Degree in medical device, life science, chemistry, or a related scientific discipline. - Minimum 7 years of experience in regulated quality systems within the medical device industry. - At least 5 years overseeing quality processes for third-party contract manufacturers or logistics operations. - Strong working knowledge of ISO 13485 requirements and quality system principles; ISO 13485 auditor certification preferred. - Demonstrated decision-making, analytical, organizational, and documentation skills. - Effective communication skills across multiple levels and functional areas. - Ability to manage multiple projects simultaneously while maintaining regulatory compliance. - Proficiency in Microsoft Office Suite and other relevant systems and tools. - Willingness to travel up to 25% for US and international engagements. Benefits - Competitive salary range of $120,000–$150,000 annually. - Health, dental, and vision insurance options. - Paid time off and flexible work arrangements. - Retirement savings and profit-sharing programs. - Professional development and training opportunities. - Supportive, collaborative, and inclusive work environment.

• The Senior Automation Engineer provides subject matter expertise in the design, implementation, and lifecycle management of digital systems • Develop system architectures and data flows for biologics, pharmaceutical, and advanced therapy manufacturing • Lead the creation, review, and approval of URS, FRS, DS / DDS, Functional & Control Narratives • Configure, program, and deploy Digital System within the manufacturing environment • Ensure all changes meet data integrity requirements, change control processes, and validation lifecycle rules • Serve as SME for troubleshooting, system optimization, batch failure analysis, and performance enhancements • Collaborate with IT/OT, process engineering, MSAT, quality, and capital project teams to deliver integrated system solutions