Process Engineer

UNAVAILABLE; Cork; Presencial; EUR 70.000 - 110.000; Jornada completa

Descripción de la vacante

Hovione in Cork, Ireland, seeks a Degree-qualified Process Engineer to lead the design, optimization and transfer of pharmaceutical manufacturing processes. You will ensure right-first-time production, support scale-ups, and drive improvements across projects with cross‑functional teams.

The role requires pharma experience, strong knowledge of GMP/HSE, and the ability to manage multiple projects and stakeholders, including customers, while maintaining compliant documentation.

Formación

• Degree in Science or Engineering, preferably Chemical Engineering.
• Mandatory pharma industry experience, incl. Fine Chemistry, Particle Engineering, Drug Product Development & Manufacturing, Process Development & Scale-up.
• Experience providing technical manufacturing support.
• Experience in equipment and technology design and in technology transfer/capital projects.

Responsabilidades

• Design, implement, optimize manufacturing processes.
• Ensure reliable, right-first-time production of intermediates and finished products.
• Support technology transfers, scale-up activities, and process improvements.
• Lead multiple process engineering projects and liaise directly with customers.
• Contribute to the design of new facilities and modification of existing installations.
• Ensure GMP/HSE compliance and prepare GMP documentation.
• Conduct risk assessments and lead CAPA investigations.
• Monitor manufacturing performance and support production activities.
• Drive productivity through process optimization and new technologies.
• Train operators and onboarding of new staff.

Conocimientos

Process Engineering

Pharmaceutical Manufacturing

GMP Compliance

HSE Awareness

Stakeholder Management

English Proficiency

Educación

Science/Engineering degree, preferably Chemical Engineering

Herramientas

SAP

Microsoft Office

Descripción del empleo

Join a Market Leader

About Hovione

At Hovione, we help partners turn scientific innovation into medicines that reach patients around the world. For more than 65 years, we have connected science, technology, and manufacturing to scale complex ideas into high-quality and innovative solutions that truly make a difference.

As an international Contract Development and Manufacturing Organization (CDMO), we support the development and manufacture of drug substances, intermediates, and drug products across the full life cycle. We are globally recognized for our leadership in specialized technologies such as Spray Drying and Continuous Tableting. But what truly sets us apart is not just what we do — it is how we do it: with purpose, care, collaboration, and a deep commitment to doing the right things right.

Our people are the reason for our success. We are a global and diverse team of more than 2,600 team members across Europe, the USA, and Asia, bringing together different experiences and perspectives to help our partners to overcome complex challenges. We believe that an inclusive environment — where everyone, regardless of background, identity or ability, is respected, heard and empowered to contribute — is essential to drive innovation, ensure quality, and secure long‑term sustainable success.

And as we grow, so do the opportunities for our people to develop, broaden their perspectives, and build meaningful careers. Because at Hovione, better starts with those who choose to make a difference every day. Will you be one of them?

You will be responsible to:

Purpose of the Role

Enable the efficient manufacture of pharmaceutical products, including highly potent compounds, while ensuring full compliance with cGMP and HSE requirements. The role is responsible for defining, implementing, improving, and supporting manufacturing processes and systems to deliver products safely, on time, within budget, and according to customer and business requirements.

Manufacturing Process Management

• Design, implement, optimize, and troubleshoot manufacturing processes.
• Ensure reliable, right-first-time production of intermediates and finished products.
• Support technology transfers, scale-up activities, and process improvement initiatives.
• Lead multiple process engineering projects and liaise directly with customers when required.
• Contribute to the design of new facilities and modification of existing installations.

GMP & Compliance

• Ensure compliance with all applicable cGMP, HSE regulations, internal procedures, and industry standards.
• Prepare and review GMP documentation including:
  • Batch Production Records (BPRs)
  • Campaign Reports
  • Change Controls
  • Validation Plans and Reports
  • Mass Balance Sheets
  • Bills of Materials (BOMs)
  • Operating Procedures and Manuals
  • Cost Proposals
• Participate in audits and inspections.

Risk Management & Investigations

• Conduct risk assessments for assigned activities and projects.
• Identify and document deviations, discrepancies, non-conformances, and abnormal events.
• Lead investigations and implement appropriate CAPAs.
• Proactively identify risks and opportunities for improvement.

Operational Support

• Monitor manufacturing performance and support production activities.
• Report equipment abnormalities and contribute to preventive and corrective maintenance activities.
• Support internal stakeholders with cost estimates, cycle times, and project-related information.
• Monitor and communicate trends impacting operational KPIs.

Continuous Improvement

• Drive productivity improvements through process optimization and introduction of new technologies.
• Evaluate and implement best practices, methodologies, and innovative solutions.
• Prepare project plans and business cases for optimization initiatives.

Training & Knowledge Sharing

• Train operators and technical teams on manufacturing processes, systems, and procedures.
• Support onboarding and qualification of new employees.
• Promote technical knowledge sharing and engineering excellence across teams.

Health, Safety & Environment

• Promote a strong safety culture and ensure compliance with all HSE requirements.
• Maintain high standards of housekeeping, hygiene, and equipment care.
• Carry out all activities safely and in accordance with company procedures and regulations.

Key Competencies

• Process Engineering
• Pharmaceutical Manufacturing
• cGMP Compliance
• Risk Assessment
• Technical Documentation
• Process Validation
• Technology Transfer
• Continuous Improvement
• Project Management
• Root Cause Analysis & CAPA
• Stakeholder Management
• Training & Coaching
• HSE Awareness
• Customer Focus

Success Measures

• On-time and right-first-time production delivery.
• Compliance with GMP and HSE requirements.
• Successful implementation of process improvements and tech transfers.
• Reduction of deviations and manufacturing inefficiencies.
• Achievement of operational and project KPIs.
• Effective support of customer and business requirements

We are looking to recruit a Candidate:

-

• Degree in Science or Engineering, preferablyChemical Engineering.
• Mandatory experience in thepharmaceutical industry, particularly in:
  • Pharmaceutical Fine Chemistry
  • Particle Engineering
  • Drug Product Development and Manufacturing
  • Process Development and Scale-up
• Experience providingtechnical manufacturing support.
• Experience inequipment and technology design.
• Experience supportingtechnology transferandcapital projects.
• Experience managing multiple projects and products from development through commercial manufacture.
• Knowledge ofGMPandHSErequirements (preferred).
• Intermediate knowledge of:
  • Organic Chemistry and/or Particle Engineering Technologies
  • Scale-up of Chemical Engineering Operations and/or Drug Product Manufacturing
• Strong project management and process improvement capabilities.
• Experience in troubleshooting, optimization, and continuous improvement initiatives.
• Strong stakeholder management and communication skills.
• Good written and spokenEnglish.
• Proficient inMicrosoft OfficeandSAP.
• Strong problem-solving, analytical, and root-cause investigation skills.
• Ability to work effectively in cross-functional teams and customer-facing environments.
• Committed to compliance, quality, safety, and operational excellence.

Hovione is a proud Equal Opportunity Employer

Inclusion and diversity are key to us. We are committed to creating an inclusive recruitment experience and welcome applications from all qualified candidates. If you require any reasonable accommodation or support during the application or interview process, please contact us, and we will be happy to assist.

Notice to Agencies and Search Firms Representatives

Hovione does not accept unsolicited resumes from agencies or search firms for this job posting. Any resumes submitted to Hovione by a third-party agency or search firm without a valid written and signed search agreement will become the sole property of Hovione. No fees will be paid if a candidate is hired for this position as a result of an unsolicited referral.