Engineering Solutions, Excellent People

About Our Company

Prochem Engineering is one of the leading engineering consultancy firms in Ireland

Prochem Engineering was established in 1995 to meet the professional consulting engineering and project management needs of the process industry in Ireland. We have grown to become one of the leading engineering consultancy firms in the country. Our clients range from indigenous companies to large multinationals which all benefit from our director-led, personal approach and our commitment to client success.

We excel in Process Engineering and Building Services Engineering, where we deliver high-quality, integrated solutions throughout the project life cycle and into the operational environment.

Separately, we operate a successful resourcing service – Tech³ – that utilises our significant technical experience for the recruitment of technical personnel to fulfil client resource requirements.

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Sectors

Prochem Sectors of Expertise

Life Sciences

Industry

Food & Beverage

Our Work

Prochem Case Studies

Chiller Upgrade

Prochem Icon on back of case study card when it flips, text overlaid.

Our client had set ambitious energy and carbon reduction targets for their site. To assist with achieving these targets, Prochem were engaged to identify and deliver energy and carbon reduction projects which included the upgrade of the chilled water plant.

New Production Laboratory

Our Client had a requirement for a new production laboratory at their distillery site. Best available technology was used to deliver a 250sq.m laboratory. The project included a sensory room where sight, smell and taste are used to assess the whiskey to develop new blends and ensure quality control.

R&D Office Renovation

Significant alterations & reconfigurations were required to our client’s existing R&D office and meeting room accommodation to meet their global standards and branding.

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Careers

Browse our job positions in all our areas of operation

Process Engineer – Product Supply

Waterford

Role Summary: Our client, based in Co. Waterford, is looking for a Process Engineer – Product Supply. Reporting to the Product Supply Team Lead, you will play an integral role within the Product Supply Unit’s team, ensuring reliable supply of syringe and vial products to our patients globally. The Product Supply APU consists of multiple platforms for the PFS inspection, assembly, labelling, cartoning, of autoinjectors and prefilled syringes and vials. The platforms range from manual processes through to high-speed, high volume automated production lines. Core Duties and Responsibilities: Provide process engineering support to the Product Supply APU. Support delivery of continuous improvement projects to existing equipment. Work closely with various departments, such as MSAT, Technical Development, Quality Assurance, and Supply Chain. Utilisation of knowledge gained from existing manufacturing technologies to aid in the development of new technologies with the goal of implementing higher output and yield. Ensure safety compliance, providing technical and engineering support for process and equipment failures, identifying, and implementing process and product improvements, supporting qualification of new products/processes, analysing machine performance data, and managing improvement projects within budget and time constraints. Support new product introductions and capacity expansions, including new vendor selections, maintenance planning, design changes, change controls, OEE improvement, yield improvement, etc. Lead systematic technical root cause investigations. Support all company safety and quality programs and initiatives. Minimum Qualifications and…

Validation Project Engineer

Tipperary

Role Summary: Our client, a pharmaceutical company in Tipperary is looking to hire a Validation Project Engineer The Validation Project Engineer is responsible for planning, executing, and managing validation activities to ensure equipment, systems, and processes meet regulatory, quality, and operational requirements. This role supports cross‑functional teams, leads validation projects from concept through completion, and ensures compliance with industry standards and internal procedures. Core Duties and Responsibilities: Lead validation projects across equipment, utilities, facilities, and manufacturing processes, ensuring timely and compliant execution. Develop and execute validation documentation, including URS, DQ, IQ, OQ, PQ, risk assessments, and validation reports. Manage project timelines, resources, and deliverables while coordinating with the wider engineering team quality, operations, and external vendors. Ensure compliance with regulatory guidelines (e.g. FDA, GAMP 5) and internal quality systems. Support equipment commissioning, FAT/SAT activities, and process qualification efforts. Analyze validation data, identify trends or issue, and recommend corrective or preventive actions. Contribute to continuous improvement initiatives, including process optimization and standardization of validation practices. Ensure that engineering, qualification and validation records are developed and maintained as per cGMP and GDP requirements Develop lifecycle activities including device innovation, concept generation, design reviews, specification development, device industrialization, manufacturing process development, validation and design verification Lead the Equipment Qualification aspects of Projects on site. Perform root cause analysis of Project issues when required.…