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Hovione

CDMO for complex drug APIs manufacturing

Senior Automation Engineer

Controls & Automation EngineeringConfirmed live in the last 24 hours
Full-timeCork, IrelandNo salary listedIn-person

About the Job

Requirements

  • A degree in Automation Engineering, Chemical Engineering, Mechanical Engineering, or a related discipline is required.
  • A minimum of 5 years of experience in industrial automation within a manufacturing environment is required.
  • Strong hands-on DeltaV programming and configuration experience is required.
  • Experience with automation system design, commissioning, qualification, and lifecycle management is required.
  • The candidate must be able to troubleshoot and resolve automation issues in live production environments.
  • Knowledge of Good Manufacturing Practice (GMP) regulations and 21 CFR Part 11 requirements is required.
  • Experience developing technical documentation, specifications, test protocols, and validation documents is required.
  • Strong problem-solving and root cause analysis skills are required.
  • Project management and stakeholder management capabilities are required.
  • Fluency in written and spoken English is required.

Responsibilities

  • Maintain, support, and optimize existing automation and process control systems.
  • Design, develop, configure, and implement automation solutions using DeltaV and associated technologies.
  • Troubleshoot and resolve complex automation issues affecting manufacturing operations.
  • Provide technical guidance and recommendations to manufacturing, engineering, and process teams.
  • Develop and maintain standards for process control, alarms, interlocks, and human-machine interfaces.
  • Support system lifecycle management, including upgrades, enhancements, and obsolescence planning.
  • Develop, review, and approve automation specifications, testing documentation, qualification protocols, and standard operating procedures.
  • Execute and support commissioning, qualification, validation, and testing activities.
  • Ensure compliance with GMP requirements, 21 CFR Part 11, and internal quality standards.
  • Participate in internal and external audits, inspections, and regulatory activities.
  • Support root cause investigations and implement corrective and preventive actions.
  • Define requirements, plan, and execute automation projects and system modifications.
  • Manage automation project activities from concept through implementation and qualification.
  • Collaborate with internal stakeholders and external contractors to ensure successful project delivery.
  • Support the development and implementation of new digital and automation technologies.
  • Drive continuous improvement initiatives across automation systems and manufacturing processes.
  • Collaborate with automation teams across Hovione sites to share best practices and standardization opportunities.
  • Contribute to annual automation objectives, resource planning, and budgeting activities.
  • Monitor and report automation system performance and project outcomes.
  • Influence automation strategy and process design decisions through technical expertise.
  • Support HSE initiatives and participate in risk assessments including PHA, FMEA, and HAZOP studies.

Desired Qualifications

  • Pharmaceutical manufacturing experience is preferred.
  • Experience within medical devices, biotechnology, oil and gas, or distillery industries using DeltaV systems is preferred.
  • Emerson DeltaV expertise is preferred.
  • Exposure to digital transformation and industrial automation innovation initiatives is preferred.

About the Company

Hovione

CDMO for complex drug APIs manufacturing

Hovione is a contract development and manufacturing organization that creates and scales active pharmaceutical ingredients (APIs) for medicines. It handles complex chemistry and specializes in processes like particle engineering and spray drying to improve drug absorption. It differentiates itself through a long history of tackling difficult compounds, deep manufacturing expertise, and an FDA-inspected global footprint across Portugal, Ireland, China, and the US. Its goal is to help drug developers bring new medicines to market efficiently by providing high-quality, scalable manufacturing and expanding capacity, especially in the U.S.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Loures, Portugal
Founded
1959

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