• Serve as the on-site electrical subject matter expert for all commissioning activities, serving as the primary escalation point for technical issues across all project phases. • Review contractor submittals, shop drawings, and O&M documentation to ensure alignment with design intent and project specifications. • Ensure Owner Project Requirements (OPR) remain aligned with commissioning scope throughout the project lifecycle, tracking changes and maintaining traceability to project objectives. • Oversee third-party commissioning agents (CxA), including scope development, performance management, deliverable tracking, and activity oversight such as factory witness testing and startup validation. • Identify equipment requiring factory testing and coordinate with the procurement team to schedule vendor testing activities. • Review and validate factory test procedures for compliance with project specifications prior to execution; oversee Factory Witness Testing (FWT) for off-site manufactured equipment. • Review and approve commissioning documentation including the Cx Plan, L2–L5 test scripts, reports, and turnover packages. • Oversee quality control processes including first-of-kind inspections and installation validation. • Drive issue identification, troubleshooting, remediation, and formal closure across all commissioning phases. • Ensure all commissioning activities — both static and dynamic testing — align with approved plans and performance standards. • Facilitate cross-functional collaboration between construction, engineering, controls, and operations teams throughout all project phases. • Manage stakeholder expectations by clearly defining commissioning processes, roles, and levels of engagement. • Ensure all commissioning documentation is complete, accurate, and supports a clean project turnover. • Support transition to operations by providing technical guidance, training coordination, and post-handover support as required. • Enforce safety, compliance, and regulatory requirements across all commissioning activities.

• Lead the field deployment, integration, and startup of automation solutions for BMS/EPMS systems, ensuring seamless integration and monitor with electrical, and cooling infrastructure. • Enforce system standards, frameworks, and deployment patterns for controls, BMS, and EPMS rollouts across multiple projects and sites. • Deploy and configure dashboards, HMIs, and operator workstations, ensuring site personnel have clear, functional visibility and control over complex building and power systems. • Oversee system integrators during standard deployments and point-to-point checkouts to ensure strict compliance with design standards, and operate as the controls escalation point to troubleshoot complex automation integration, system inconsistencies, and network integration issues. • Collaborate with design engineers, contractors, and OEM partners in the field to configure, integrate, and troubleshoot networks utilizing BACnet, Modbus, OPC-UA, and MQTT protocols. • Conduct system testing, simulation, Factory Acceptance Testing (FAT), and Site Acceptance Testing (SAT) to validate functionality, sequencing, and data accuracy prior to operational handover. • Ensure controls platforms correctly collect and push real-time and historical data, enabling performance insight and analysis. • Mentor and train other controls engineers, on control system operation, troubleshooting best practices, and execution methodology.

• Execute productivity initiatives to deliver long-range strategic plan for Doors, working with internal and external resources. • Facilitate cross functional team collaboration to deliver improved results. • Build capability of our operations to meet customer needs and replicate equipment and process standards across the network. • Work closely with operations, stable ops, and supply chain to identify opportunities and execute change effectively

Role Description Responsible for the execution of validation projects for equipment, facilities, and utilities in a pharmaceutical manufacturing, packaging, or support environment. - Coordinate execution efforts with operations, manufacturing, facilities, laboratories, development, materials management, and quality assurance personnel. - Analyze validation data, prepare summary reports, and provide recommendations for improvement in manufacturing processes and equipment. - Develop training packages, JSAs, and writing Best Known Methods (BKM) for Validation. - Serve as a dependable liaison between validation and manufacturing. - Identify, respond to, and monitor potential project risks and determine possible contingency plans for risk mitigation. - Review technical and quality system documents such as SOPs, Change Control and Deviation Reports, Batch Production Records, Technical Manuals, P&IDs, construction, as-built, and flow diagrams as they relate to validation principles and regulatory compliance issues. Qualifications - Bachelor’s degree (or foreign degree equivalent) in Engineering, Science, or a related technical field. - Must have 2 years of experience as a Validation Engineer, Automation Engineer, Technical Writer, or a related occupation in an Equipment Qualification in Biotechnology or Pharmaceutical GMP environment. - Demonstrated experience in/with: - Developing Engineering Lifecycle Documents (URS, FRS, DDS, FRAs) and Validation Protocols (IQ, OQ, PQ, AIQ, VSR, PVP). - Change control processes in the pharmaceutical industry. - 21CFR 210, 211, and Part 11. - Data Integrity Requirements for Electronic Records and Signatures per 21CFR Part 11. - Performing validation activities for SCADA, WinCC OA, and PI tags for Building Automation Systems and Environmental Monitoring Systems. - Developing and executing FATs, SAT, and Startup testing for automated systems. Requirements - 100% telecommuting role; may work from any location inside the U.S. - reports to company office in Durham, NC. - Up to 10% travel to various unanticipated worksites within the U.S. is required. - Must have legal authority to work in the U.S. How to Apply Send resumes to Michael Hammond, HR & Safety Director, Mangan, Inc., 3880 Kilroy Airport Way, Suite 100, Long Beach, CA 90806, or email to mhammond@manganinc.com. Please reference job title + SR26 in cover letter or email subject line.