CQV Engineer Location: Dublin, County Dublin, Ireland Job Description: Key Responsibilities: Work closely with the Area CQV Lead to plan, prepare, and execute commissioning and validation activities for Utilities Develop and execute CQV testing documentation for Utilities and HVAC systems Deliver key project milestones related to safety, CQV schedule, and quality of documentation/electronic records. Ensure testing of GMP equipment, Utilities, and HVAC systems is performed in compliance with GMP requirements, company policies, and EU/FDA regulations. Ensure all Utilities, and HVAC systems are commissioned and tested in line with project standards. Lead or support management of deviations related to assigned systems and utilities. Identify and assess CQV risks; develop and implement mitigation plans. Execute FAT testing and incorporate results into the overall qualification lifecycle. Complete all required training in line with project and site metrics. Work effectively within a diverse CQV team to deliver work safely, on schedule, and within budget. Proven ability to execute CQV activities from initiation through handover. Strong experience in the CQV project lifecycle: design, commissioning, qualification, and validation. Demonstrated experience with HVAC systems in controlled environments. Experience with Utilities, including: High Purity Water systems Clean Steam High Purity Gas Systems Strong documentation, execution, and task planning skills with consistent on-time delivery. Excellent communication and stakeholder influencing skills. Experience working in matrix teams and cross‑functional project environments. Familiarity with electronic validation systems (e.g., ValGenesis, Kneat). Qualifications & Experience: Bachelor’s degree in a scientific, engineering, or technical discipline (minimum requirement). Minimum 5 years’ experience in the pharmaceutical industry Proven experience in CQV of HVAC and Utility Systems Seniority Level: Mid‑Senior level Employment Type: Full‑time Job Function: Engineering, Quality Assurance, and Manufacturing Industries: Engineering Services, Pharmaceutical Manufacturing, and Biotechnology Research #J-18808-Ljbffr
Arcadis DPS Engineering are seeking a Packaging Maintenance Technician for a pharmaceutical assignment located in Carrigtwohill, Cork. This is a 12-month contract initially. Responsibilities Perform preventive maintenance on packaging equipment in accordance with CMMS (Maximo) schedules. Independently diagnose and resolve equipment failures, utilising technical drawings, specifications, manuals, and electronic test equipment. Execute corrective maintenance and replace defective components on packaging production lines. Respond promptly to equipment emergencies to minimise production downtime. Maintain accurate and timely maintenance and repair records within the CMMS system. Adhere to current Good Manufacturing Practices (GMP), EHS regulations, and site safety policies in all activities. Promote and maintain a strong safety culture within the maintenance team and across the site. Utilise hand tools, power tools, and electronic test equipment for maintenance tasks. Support continuous improvement initiatives aimed at enhancing equipment reliability and performance. Identify and implement opportunities for process and maintenance improvements, following established SOPs and company policies. Requirements Degree or Trade Qualification in a relevant science or engineering discipline. Minimum 2-3 years’ experience in an engineering or technical role within a pharmaceutical manufacturing environment. Proven experience in preventive and corrective maintenance of packaging equipment (experience with Maximo CMMS is highly desirable). Strong technical troubleshooting skills in both mechanical and electrical systems. Excellent verbal, written, and interpersonal communication skills, with the ability to work independently and collaboratively. Why Join Arcadis? At Arcadis, we empower individuals to excel because your contributions matter. Taking a skills-based approach, we provide opportunities for you to shape your career, maximize your impact, and grow professionally. By joining us, you’ll engage in meaningful work that drives sustainable solutions for a better planet while leaving a lasting legacy. Our Commitment to Equality, Diversity, and Inclusion We are dedicated to creating an environment where everyone can thrive. Through our six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race— we foster innovation by bringing together diverse perspectives. Together, we strive to improve quality of life while building a more inclusive future. #J-18808-Ljbffr
A leading engineering firm in Carrigtwohill, Cork is seeking a Packaging Maintenance Technician on a 12-month contract. The role involves performing preventive and corrective maintenance on packaging equipment while adhering to GMP and safety policies. The ideal candidate has a degree or trade qualification in a relevant field and 2-3 years of experience in a pharmaceutical manufacturing environment. Opportunities for continuous improvement and a commitment to safety are encouraged. #J-18808-Ljbffr
A leading engineering services firm in Dublin is seeking a CQV Engineer to manage commissioning and validation activities for Utilities and HVAC systems. The ideal candidate has over 5 years of experience in the pharmaceutical industry and a strong background in CQV project lifecycles. This full-time role offers the opportunity to work closely with diverse teams to ensure compliance with quality and safety standards. #J-18808-Ljbffr
A leading global engineering firm in Ireland is seeking an experienced NPI Process Engineer to lead the delivery of capital engineering projects from design to operational handover. You will collaborate with cross-functional teams and ensure that all equipment complies with GMP and safety regulations. Ideal candidates will have over 5 years of experience in a GMP environment and a relevant engineering degree. This role offers a 12-month contract with a strong prospect of extension. #J-18808-Ljbffr
About Arcadis Arcadis is the world’s leading company in sustainable design, engineering, and consultancy for natural and built assets. With over 36,000 professionals across 70+ countries, we are united in our mission to improve quality of life and solve the world’s most complex challenges. Be part of something meaningful – join us! Job Summary: In this NPI Process Engineer job, you will spearhead the delivery of capital engineering projects and new product introductions across the full project lifecycle from concept design through to operational handover. You will provide technical expertise to ensure systems and equipment are installed, commissioned, and qualified in line with GMP and regulatory expectations. This will be an initial 12-month contract with strong prospect of extension Main Duties: As NPI Process Engineer, your job will be to work closely with cross-functional New Product Introduction (NPI) teams to interpret process requirements and collaborate with automation engineers on the design of process control strategies. Prepare and execute commissioning, qualification, and verification protocols for new or modified process equipment and associated automation systems. Provide technical support and troubleshooting during initial production batches for new or transferred processes. Ensure all installed equipment meets safety, quality, and regulatory requirements. Adhere to all engineering policies, technical procedures, and compliance standards. Represent engineering on project teams, providing subject matter expertise and guiding the resolution of technical issues throughout the project lifecycle. Ensure projects remain on schedule and within scope, working proactively with internal stakeholders to overcome challenges and meet delivery timelines. Support a culture focused on high-quality, Right-First-Time execution in partnership with Operations, Project Engineering, and NPI teams. Contribute technical input during internal and external audits and be prepared to present/defend engineering systems, change controls, investigations, and qualification documentation as required. Your background: For this NPI Process Engineer job, you will have 5+ years’ experience in a similar role in a GMP pharmaceutical environment. You will also have a relevant degree in engineering or a related discipline and experience commissioning/qualifying process equipment. Why Join Arcadis? At Arcadis, we empower individuals to excel because your contributions matter. Taking a skills-based approach, we provide opportunities for you to shape your career, maximize your impact, and grow professionally. By joining us, you’ll engage in meaningful work that drives sustainable solutions for a better planet while leaving a lasting legacy. Our Commitment to Equality, Diversity, and Inclusion We are dedicated to creating an environment where everyone can thrive. Through our six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race—we foster innovation by bringing together diverse perspectives. Together, we strive to improve quality of life while building a more inclusive future. #J-18808-Ljbffr
A leading pharmaceutical firm in Ireland, Munster is seeking a QA Validation Specialist. The ideal candidate will have a BSc or equivalent qualifications, with strong reviewing skills and attention to detail. Responsibilities include managing GxP validation activities, ensuring compliance with regulatory requirements, and participating in project teams related to validation documentation. Experience in the pharmaceutical industry is preferred. #J-18808-Ljbffr
A leading engineering consultancy in Dublin is seeking an NPI Process Engineer to spearhead the delivery of capital engineering projects. The ideal candidate will have over 5 years of experience in a GMP pharmaceutical environment and a relevant engineering degree. This role involves managing projects from concept design to operational handover, ensuring compliance with regulatory expectations. Join a company dedicated to sustainability and professional growth. #J-18808-Ljbffr
About Arcadis Arcadis is the world’s leading company in sustainable design, engineering, and consultancy for natural and built assets. With over 36,000 professionals across 70+ countries, we are united in our mission to improve quality of life and solve the world’s most complex challenges. Be part of something meaningful – join us! Join us and contribute to transformative projects that drive sustainability and create lasting value for communities worldwide. Job Summary In this NPI Process Engineer role, you will spearhead the delivery of capital engineering projects and new product introductions across the full project lifecycle from concept design through to operational handover. You will provide technical expertise to ensure systems and equipment are installed, commissioned, and qualified in line with GMP and regulatory expectations. This is an initial 12-month contract with strong prospect of extension. Main Duties Work closely with cross‑functional New Product Introduction (NPI) teams to interpret process requirements and collaborate with automation engineers on the design of process control strategies. Prepare and execute commissioning, qualification, and verification protocols for new or modified process equipment and associated automation systems. Provide technical support and troubleshooting during initial production batches for new or transferred processes. Ensure all installed equipment meets safety, quality, and regulatory requirements. Adhere to all engineering policies, technical procedures, and compliance standards. Represent engineering on project teams, providing subject matter expertise and guiding the resolution of technical issues throughout the project lifecycle. Ensure projects remain on schedule and within scope, working proactively with internal stakeholders to overcome challenges and meet delivery timelines. Support a culture focused on high‑quality, Right‑First‑Time execution in partnership with Operations, Project Engineering, and NPI teams. Contribute technical input during internal and external audits and be prepared to present/defend engineering systems, change controls, investigations, and qualification documentation as required. Your background 5+ years of experience in a similar role in a GMP pharmaceutical environment. Relevant degree in engineering or a related discipline and experience commissioning/qualifying process equipment. Why Join Arcadis? At Arcadis, we empower individuals to excel because your contributions matter. Taking a skills‑based approach, we provide opportunities for you to shape your career, maximize your impact, and grow professionally. By joining us, you’ll engage in meaningful work that drives sustainable solutions for a better planet while leaving a lasting legacy. Our Commitment to Equality, Diversity, and Inclusion We are dedicated to creating an environment where everyone can thrive. Through our six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race—we foster innovation by bringing together diverse perspectives. Together, we strive to improve quality of life while building a more inclusive future. #J-18808-Ljbffr
QA Validation Specialist – Kerry The successful QA Validation Specialist will be qualified with a BSc or equivalent academic qualifications with previous Industrial/pharmaceutical experience an advantage. Strong reviewing skills and attention to detail to ensure right first time with GxP Validation or validation governance experience an advantage. GxP Change Control experience also an advantage. Duties: Involvement in the development, improvement and control of GxP validation activities. QA Final approval compliance governance function. Reviewing and approving validation documentation, e.g. User Requirement Specifications, Validation Plans, OQ, PQ, Validation Protocols/ Reports, Qualification Data etc. Ensuring compliance with AICL(KP) procedures and regulatory requirements. Participation in project teams to advise and assist in ensuring that validation documentation is written and executed in accordance with internal validation procedures, policies and adheres to the principles of cGxP. Familiarisation with developments, evolving regulatory requirements and innovations in validation requirements. QA Management of site GxP change control processes, ensuring maintenance of GxP compliance, procedural compliance and of the validated state. QA Management of Computerised System Periodic Reviews to ensure maintenance of the validated state. Generation of the site Product Quality Reviews for GxP change control activities. Biannual Trend Review of GxP site change controls. Equal Opportunities Employer. #J-18808-Ljbffr
