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.
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