Process Engineer - II

Occupli Limited; Carlow; On-site; EUR 45,000 - 65,000; Full time

Job summary

A leading engineering support company in Carlow is seeking a motivated Process Engineer. This role involves providing technical support for a key pharmaceutical manufacturing client, focusing on new product introductions and continuous improvement initiatives. The ideal candidate will have a degree in engineering and at least 3 years' relevant experience in the pharmaceutical sector. You will engage in process optimisation and ensure adherence to safety and quality standards.

Qualifications

• Minimum 3 years’ experience in a manufacturing or process engineering role.
• Demonstrated experience in technology transfer and process optimisation.
• Knowledge of regulatory requirements and industry standards is essential.

Responsibilities

• Provide engineering support for new product introductions.
• Develop and execute validation and qualification protocols.
• Drive continuous improvement projects using Lean Six Sigma principles.

Skills

Experience in manufacturing or process engineering

Technology transfer expertise

Problem-solving skills

Excellent communication

Teamwork

Education

Degree in Engineering, Science, or related technical discipline

Tools

DeltaV automation systems

Pi data systems

Job description

Overview

Job Description – Process Engineer (Pharmaceutical ClientSupport)

Location: Carlow, Ireland

Reports to: Technical Engineering Manager (Occupli Assignment)

Contract Type: Full-time contract

About the Role

Occupli is seeking a motivated Process Engineer to join our team and support a key pharmaceutical manufacturing client. This role offers an exciting opportunity to work at the interface of engineering, manufacturing, and technical services, with a focus on new product introduction, process optimisation, and continuous improvement initiatives.

The successful candidate will provide technical and operational support to ensure smooth technology transfer, reliable manufacturing performance, and adherence to quality and safety standards. You will collaborate with cross-functional teams and external partners, contributing to both routine operations and strategic improvement projects.

Responsibilities

• Provide engineering support for new product introductions (NPI) and commercial manufacturing activities.
• Develop, review, and execute validation and qualification protocols for equipment, processes, and systems.
• Prepare and manage change controls, risk assessments, and technical reports.
• Investigate deviations and process issues, supporting root cause analysis and implementing corrective/preventive actions.
• Drive and participate in continuous improvement projects, applying Lean Six Sigma principles.
• Contribute to process development studies and data-driven decision-making.
• Collaborate with automation, utilities, validation, and quality teams to support manufacturing operations.
• Ensure work practices comply with GMP, safety, and regulatory standards at all times.
• Represent the engineering function during internal and external audits as required.

Qualifications & Experience

• Degree in Engineering, Science, or a related technical discipline.
• Minimum 3 years’ experience in a manufacturing or process engineering role (pharmaceutical, biotechnology, or related industries preferred).
• Demonstrated experience in technology transfer, validation, and process optimisation.
• Knowledge of automation systems (e.g., DeltaV), process monitoring, or data systems (e.g., Pi) is advantageous but not essential.
• Familiarity with regulatory requirements and industry standards (Irish, European, and international).
• Excellent communication, teamwork, and problem-solving skills.
• Opportunity to work on challenging, high-impact projects within a global pharmaceutical environment.
• Exposure to cutting-edge facilities and diverse engineering disciplines.