Engineer II, Integration

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description How You Will Make an Impact: The Engineer II, Integration supports the integration, configuration, testing, and commissioning of automation and bioprocessing systems within Product Engineering, ensuring systems are accurately configured and prepared for Factory Acceptance Testing (FAT) and customer delivery. The role contributes to the transition from engineering requirements and system components to complete, tested, documented, and supportable automation solutions ready for customer acceptance and delivery. This role independently executes assigned system-integration and configuration activities, troubleshoots hardware, software, network, and configuration issues, and resolves technical problems within established engineering standards and procedures while collaborating cross-functionally to support system readiness, reduce integration-related risks, and improve execution. Location: Santa Clara, CA . Relocation assistance is NOT provided. • Must be legally authorized to work in the United States without sponsorship. • Must be able to pass a comprehensive background check, which includes a drug screening. What will you do?: Review system architecture, build definitions, technical documentation, and customer requirements to ensure assigned integration activities are executed accurately. Identify integration-related risks, dependencies, or schedule impacts and communicate or escalate issues appropriately to support project commitments. Build, configure, and verify assigned system infrastructure, including servers, virtual machines, network settings, system communications, software configurations, and related integration components in accordance with approved system architecture and established engineering requirements. Configure and verify assigned DeltaV, TruBio, HCI, server, network, and automation-system components, including system communications, controllers, I/O, operator interfaces, alarms/events, historians, user/security functions, and other applicable features in accordance with approved system architecture and project requirements. Configure and verify assigned TruBio control areas and vessel configurations for applicable single-use equipment, including process parameters, instrumentation, alarms, interlocks, engineering units, ranges, and customer-specific options in accordance with approved system requirements. Configure, test, and troubleshoot communications and interfaces between automation systems and single-use equipment, controllers, PLCs, I/O, instrumentation, Modbus devices, and supported third-party equipment. Configure and verify applicable operator graphics, system navigation, user access, historians, alarms/events, and other operator-facing automation functionality. Independently execute assigned system-integration activities for standard and moderately complex customer configurations, escalating highly complex or non-standard technical issues as appropriate. Maintain accurate and controlled system build records and complete required as-built documentation and system backups, including applicable automation configurations, controllers/I/O, licensing information, and supporting technical documentation, in accordance with established procedures. Document technical issues, troubleshooting activities, configuration changes, test results, and resolutions accurately and in accordance with applicable engineering and quality requirements. Verify system configuration, connectivity, functionality, documentation, and overall readiness prior to Factory Acceptance Testing (FAT). Independently troubleshoot routine-to-complex hardware, software, network, communications, and configuration issues; apply structured problem-solving methods to identify root causes, implement corrective actions within established technical standards, verify effective resolution, and escalate highly complex or systemic issues as appropriate. Prepare assigned systems for FAT, customer acceptance, shipment, installation, and subsequent service support by ensuring configuration, documentation, backups, and required technical records are complete and accurate. Support FAT execution from an integration perspective by ensuring system readiness, resolving assigned technical issues, implementing approved configuration changes, and coordinating with Validation, Engineering, and project stakeholders. Partner with Validation, Manufacturing Engineering, Product Engineering, Project Management, Manufacturing, Service, and other stakeholders to resolve integration issues and support project execution. Provide technical input during project discussions and customer-facing activities within assigned areas of responsibility. Support Service activities for installed systems, expansions, modifications, backup/restoration, and troubleshooting of assigned automation, configuration, networking, communications, and control-system issues. Support NPI activities by executing assigned integration, configuration, commissioning, testing, documentation, and system-readiness activities for new equipment, automation platforms, and product enhancements; identify integration gaps and technical risks and communicate lessons learned to the appropriate Engineering stakeholders. Identify and implement improvements to integration procedures, checklists, technical documentation, troubleshooting practices, and standard workflows to improve quality, repeatability, cycle time, and execution efficiency. Participate in or lead assigned PPI/continuous improvement activities within the scope of the role. Configure, document, and verify assigned automation-system features that support applicable GMP, data-integrity, and 21 CFR Part 11 requirements, including user access/security, audit trails, alarms and events, electronic records, system history, and other compliance-related functions as defined by system and customer requirements. Perform and independently execute assigned integration, configuration, testing, and commissioning activities for automation and bioprocessing systems in accordance with approved system architecture, customer requirements, engineering documentation, and project schedules. Support custom and non-standard system configurations under appropriate engineering direction and within established design requirements. Manage multiple assigned integration activities and project priorities while meeting established schedules and quality requirements. Share technical knowledge and provide informal guidance or peer support to colleagues within areas of demonstrated expertise. Perform other duties as assigned. The responsibilities described above are representative of the nature and level of work performed and are not intended to be an exhaustive list of all duties and responsibilities. Education & Experience: Required: Advanced Degree in Engineering, Computer Science, Automation, Controls, or a related technical discipline; OR Bachelor's Degree in Engineering, Computer Science, Automation, Controls, or a related technical discipline with 2 years of experience in supporting automation, control systems, system integration, commissioning, validation, or other technically complex engineered systems; OR Associate Degree in Engineering, Computer Science, Automation, Controls, or a related technical discipline with 4 years of experience in supporting automation, control systems, system integration, commissioning, validation, or other technically complex engineered systems; OR High School Diploma or equivalent with 6 years of experience in supporting automation, control systems, system integration, commissioning, validation, or other technically complex engineered systems. Experience configuring, integrating, testing, or commissioning automation, control, computer/network, or other technically complex systems. Experience troubleshooting hardware, software, network, communications, or system-configuration issues. Experience working with technical documentation, system architectures, configuration requirements, or test procedures. Experience working cross-functionally within engineering, manufacturing, validation, service, or project environments. Preferred: Experience with DeltaV, TruBio, HCI, PLC/SCADA, or comparable industrial automation/control platforms. Experience with virtualization technologies, servers, networking, and system infrastructure. Experience configuring or troubleshooting industrial networks, communications, and integrated automation systems. Experience supporting Factory Acceptance Testing (FAT), commissioning, system qualification, or validation activities. Experience with single-use bioprocessing equipment, bioreactors, mixers, or related capital equipment. Experience in biotechnology, pharmaceutical, medical-device, or other GMP-regulated manufacturing environments. Experience supporting customer-configured or engineer-to-order systems. Knowledge, Skills, Abilities: Required: Strong working knowledge of automation and system-integration principles applicable to industrial or bioprocessing equipment. Working knowledge of automation platforms, control systems, servers, virtualization, networking, communications, instrumentation, and integrated system architectures used in industrial or bioprocessing applications. Working knowledge of system configuration, user access/security, alarms/events, historians, control-system interfaces, and other automation features applicable to assigned systems. Ability to independently configure, integrate, test, and troubleshoot assigned automation and system components within established engineering standards and procedures. Strong technical troubleshooting and problem-solving skills with the ability to diagnose hardware, software, network, communication, and configuration issues. Ability to understand and interpret system architectures, network diagrams and configurations, server/virtualization environments, technical specifications, configuration requirements, test procedures, and engineering documentation sufficient to configure, integrate, test, and troubleshoot assigned systems. Ability to identify technical risks, dependencies, and configuration issues and escalate non-routine or high-impact issues appropriately. Ability to perform and verify approved system backup and restoration activities for assigned automation configurations and supporting system components. Strong attention to detail and commitment to system configuration accuracy, documentation quality, and repeatable execution. Strong organizational and prioritization skills with the ability to manage multiple assigned projects and integration activities. Effective cross-functional communication skills with the ability to collaborate with Engineering, Validation, Manufacturing, Project Management, Service, and other stakeholders. Ability to communicate technical issues, troubleshooting findings, risks, and recommendations clearly to technical and non-technical stakeholders. Ability to work independently within established engineering standards, procedures, and technical direction. Ability to document system configurations, test results, troubleshooting activities, and technical resolutions accurately. Ability to share technical knowledge and provide peer guidance within areas of demonstrated expertise. Working knowledge of applicable quality, safety, configuration-management, and regulated-environment requirements. Working knowledge of GMP, data-integrity, 21 CFR Part 11, quality-system, and validation requirements applicable to automation and control systems. Proficiency with applicable engineering, automation, configuration, documentation, and Microsoft Office/business systems. Preferred: Knowledge of DeltaV, TruBio, HCI, PLC/SCADA, or related automation platforms. Knowledge of Windows Server, virtualization technologies, networking, TCP/IP, and related infrastructure. Familiarity with industrial communication protocols and network architectures. Knowledge of FAT, commissioning, validation, and equipment qualification practices. Knowledge of single-use bioprocessing equipment and related technologies. Familiarity with Lean Manufacturing, PPI, or continuous improvement methodologies. Physical Requirements and Work Environment: Combination of office-based engineering work and regular activity within integration, laboratory, FAT, manufacturing, and testing areas. Regular use of computers, automation systems, engineering/configuration tools, and business systems for extended periods. Frequent standing and walking within integration and FAT areas to configure, test, troubleshoot, and evaluate systems. May require bending, reaching, crouching, or accessing equipment, control panels, servers, network hardware, cables, or system components during integration and troubleshooting activities. Required use of appropriate PPE when entering designated manufacturing, laboratory, integration, testing, or controlled areas. Exposure to electrical equipment, automation hardware, manufacturing equipment, and moderate noise levels as applicable to the work environment. Occasional lifting or movement of tools, cables, components, computer/network equipment, or related materials up to 25 lbs. Role requires regular onsite presence to support system integration, testing, FAT activities, and project execution. May require schedule flexibility to support FAT activities, project deadlines, system troubleshooting, customer commitments, or other business-critical activities. Apply today! We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, company 401k, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation. Compensation and Benefits The salary range estimated for this position based in California is –. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: