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Lonza

Global life sciences contract manufacturer

Senior Automation, Instrumentation & Controls Engineer

Controls & Automation EngineeringPosted on Nov 11
Full-timePortsmouth, NH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in Engineering, Automation Engineering, Electrical Engineering, Chemical Engineering, Computer Engineering, or a related technical discipline.
  • Significant experience supporting GMP manufacturing automation and process control systems within the biopharmaceutical, pharmaceutical, biotechnology, or regulated manufacturing industry.
  • Demonstrated experience leading complex controls engineering projects and technology transfers.
  • Strong experience with DeltaV, programmable logic controllers, process instrumentation, and industrial automation systems.
  • Proven success leading technical investigations, root cause analysis activities, and complex troubleshooting efforts.
  • Experience supporting commissioning, qualification, validation, and startup activities within regulated environments.
  • Expertise in automation system architecture, process control strategies, and manufacturing execution environments.
  • Strong understanding of GMP regulations and computerized system compliance requirements.
  • Experience with PI Historian, change management systems, and electronic quality management platforms.
  • Knowledge of process instrumentation, networking, industrial communications, and batch control systems.
  • Familiarity with risk assessment methodologies and lifecycle management principles.

Responsibilities

  • Provide senior technical leadership and oversight for GMP automation, instrumentation, and control systems supporting manufacturing operations.
  • Lead complex technical support, reliability improvement, and lifecycle management activities across assigned manufacturing processes and controls platforms.
  • Establish technical approaches and engineering strategies for ambiguous or complex assignments requiring independent judgment and risk-based decision making.
  • Serve as the primary Controls subject matter expert for Manufacturing, MSAT, Engineering, Quality, and project teams.
  • Lead the design, implementation, testing, and deployment of complex automation changes involving Emerson DeltaV distributed control systems, programmable logic controller-based control systems, process instrumentation and field devices, I/O architectures and communication networks, OPC/Kepware interfaces, and batch reporting and data collection systems.
  • Own complex control system modifications and provide technical review and approval of engineering documentation, including P&ID updates and work orders.
  • Develop and approve automation strategies that balance manufacturing needs, system reliability, lifecycle sustainability, and regulatory compliance.
  • Lead Controls and Automation scope for capital projects, process expansions, and technology transfer activities.
  • Develop project estimates, schedules, resource plans, risk assessments, and contractor management strategies.
  • Coordinate cross-functional activities to ensure successful implementation and startup of automation-related projects.
  • Drive stakeholder alignment while managing competing project priorities.
  • Lead high-complexity troubleshooting efforts across manufacturing systems and control platforms.
  • Use historian data (OSIsoft PI), code reviews, configuration assessments, root cause analysis methodologies, and cross-functional investigations to identify and resolve system issues.
  • Assess process and automation risks and recommend corrective and preventive actions to prevent recurrence.
  • Support manufacturing operations during critical events and participate in site on-call support activities.
  • Author, review, and approve functional specifications, design specifications, configuration specifications, test protocols, and validation documentation.
  • Define testing strategies and lead factory acceptance testing, site acceptance testing, commissioning, startup, and validation-support activities.
  • Own and approve quality records including deviations, corrective and preventive actions, investigations, and change controls.
  • Ensure documentation is completed within Kneat, TrackWise, DMS, and Veeva systems in accordance with site procedures and regulatory requirements.
  • Ensure compliance with GAMP 5, ISA-88, 21 CFR Part 11, EU Annex 11, applicable GMP regulations, and corporate standards.
  • Represent Controls Engineering in governance forums, Integrated Project Teams, Joint Project Teams, customer discussions, client audits, and regulatory inspections.
  • Provide technical mentoring and coaching to automation and controls engineers.
  • Lead technical reviews, establish engineering standards, and share lessons learned across the organization.
  • Provide direction and oversight to contractors, integrators, and project resources.

About the Company

Lonza

Global life sciences contract manufacturer

Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1897

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