Archives: Jobs

Role Summary: We are seeking a reliable and organised Part-Time Administrator to support operations at a pharmaceutical manufacturing facility in Kildare. This role will be 3 days a week on site in Kildare. Core Duties and Responsibilities: Coordinate employee training schedules and maintain training records Assist with new starter inductions and onboarding activities Support day-to-day […]

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 Experience: Experience in a highly regulated GMP environment. Degree in an Engineering discipline. Strong problem solving and communication skills. Strong documentation/protocol generation and execution skills. Strong data analysis experience with equipment and integrated systems is desirable. Please note, we do not require agency assistance with this role.

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. Effectively communicate and discuss related day to day activity and concerns within the team for efficiency and performance improvement Coordinate with design consultants as required and respective user departments for the design/manufacturing of equipment Review and approval on detailed designs as submitted by vendors Ensure project execution work and follow ups with different depts (QA, QM, Operations) to meet project completion within stipulated time frame Minimum Qualifications and Experience: Level 7 /8 degree in Engineering, Science, or a related technical field. 5+ years of experience in validation, engineering, or quality roles within pharmaceutical, biotech, medical device, or similar regulated industries. Strong knowledge of validation principles, GxP requirements, and risk‑based approaches. Experience with equipment qualification, process validation, and/or computer system validation is an advantage. Excellent project management, documentation, and communication skills. Ability to work independently and collaboratively in a fast‑paced environment. Experience with automation systems, data integrity principles, or digital validation tools Please note, we do not require agency assistance with this role.

Role Summary: Our client is looking for a Construction Manager based in Co. Waterford. The Construction Lead / Manager will be responsible for the overview of several projects at the site in Waterford – primarily civil / structural related projects. Core Duties and Responsibilities: Proactively ensure a positive safety culture at the site adopting an […]

Role Summary: A new opportunity has arisen for an experienced PMO Project Engineer to join our client’s new manufacturing site in Co. Kilkenny. You will be responsible for leading key elements of the program and acting as the program voice for your given workstream. You will also take ownership of the successful implementation of a […]

Role Summary: Our client, a leading pharmaceutical organisation is seeking to hire an EHS Specialist on a 12-month contract, on site in Co. Wicklow. The EHS Support Specialist, reporting to the Capital Project Lead, takes responsibility and ownership for all EHS activities associated with the Automation & Electrical Upgrade project. The role is responsible for […]

Role Summary: A new opportunity has arisen for an Electrical Engineer to join our client’s pharmaceutical facility in Co. Wicklow. This position reports directly to the Engineering Capital Lead and supports delivery of the Wicklow Site capital project by providing electrical engineering oversight to ensure all electrical systems are designed, installed, commissioned, and maintained in […]

Role Summary: A new vacancy has arisen for a Project Portfolio Lead supporting our client’s Project Portfolio Management group based on their bio-pharmaceutical site in Co. Waterford. The Project Portfolio Management group provides oversight and delivers projects for the Waterford site and to the benefit of the patients and the company. We are looking for […]

Role Summary: Our client, a biopharmaceutical company based in Co. Waterford, is seeking a Regulatory Site Officer to join their Regulatory Affairs Department, responsible for managing products manufactured at Waterford from a regulatory perspective; ensuring submissions are submitted on time, assessing change controls and deviations and ensuring regulatory compliance. The team is an energetic and […]

Role Summary: An exciting new opportunity has arisen for a Project Engineer (Equipment) to join our client’s busy biopharmaceutical facility in Co. Waterford. We are looking for an accountable project engineer to deliver a diverse project portfolio assignment. Delivery of this project portfolio will be within the biopharmaceutical operations which include enzyme, monoclonal antibodies (mAbs), oral […]

Role Summary: Our client, in the pharmaceutical sector, is seeking to hire a CSV Specialist to join their team. This position reports directly to the Engineering Capital Lead and as CSV Specialist/Engineer, will act as the site Computer System Validation (CSV) Subject Matter Expert for the duration of the major Capital Project. Provide CSV leadership […]

Role Summary: A new vacancy has arisen for an experienced Automation Engineer supporting our client’s Automation Team. The successful candidate will play an integral role in providing automation support and expertise across multiple departments on a busy pharmaceutical site. Core Duties and Responsibilities: Work with the Automation Team to provide Automation support for operations and […]

Graduate Applications for 2026: We are now taking applications for our 2026 Graduate Program. Joining Prochem Engineering’s Graduate Program is an extraordinary opportunity to embark on a journey of professional growth and development. Over the 18 Month program, you will have the privilege of learning from some of the most brilliant minds in the industry, […]

Role Summary: We are currently recruiting for a Process Engineer to join the engineering design team for projects in the Bio-pharmaceutical, API and Food Science manufacturing sectors, delivering concept, front end & detail design engineering activities. To manage activity planning, work scheduling, assigning responsibilities to the team, and ensuring deliverables can be met. Core Duties […]

Role Summary: We have an immediate requirement for a Lead Building Services Engineer to work as part of an established design team in our Cork Office. To manage activity planning, work scheduling, assigning responsibilities to the team, and ensuring deliverables can be met. Core Duties and Responsibilities: Leading the design of a range of HVAC […]