A leading engineering consultancy is looking for a Director of Project Controls to lead initiatives and set standards for project controls in Dublin or Cork. The role demands a degree and significant experience in managing project controls for large-scale pharma projects. Responsibilities include developing strategies, ensuring compliance, and mentoring teams. This is an opportunity to shape impactful solutions and drive a legacy of excellence in the industry. #J-18808-Ljbffr
Director of Project Controls Ireland About Us. As an Arcadian, you already help us deliver world leading sustainable design, engineering, and consultancy solutions for natural and built assets. You are part of our global business comprising 36,000 people, in over 70 countries, dedicated to improving quality of life. Everyone has an important role to play. With the power of many curious minds, together we can continue to solve the world’s most complex challenges and deliver more impact together. Location/s Based in our Dublin or Cork Role description The Director of Project Controls will be a key role within the Ireland Management team. The role will involve the development and implementation of a strategy that will strengthen our Projects Controls function across the following key areas: Project services Project Planning/scheduling Project cost estimating Contract Procurement and Administration The role will involve working closely with the Business directors and project managers to set standards, support the development of project execution strategies, support the built of appropriate project teams and act as a peer reviewer on the projects to identify risks and mitigation strategies. The role will have a Utilisation target of 60% Reporting lines Direct reporting line to EU Pharma BU Director and dotted line to Business Directors in Dublin and Cork. Role accountabilities Work closely with Business Directors, Project Managers and Department managers to ensure successful delivery of Project Controls function. Support/Review of Project Controls Proposals. Participate in Corporate and outside industry committees and bodies. Assist with the development of the long-term business strategy, reflective of business trends, in conjunction with the Business Directors, to ensure that the project Controls Function is providing an efficient and effective service. Duties & Responsibilities Provide strong leadership in setting standards for project controls Responsible for the improvement of the Projects Controls procedures, work instruction and guidelines. Audit Operations/projects for compliance with procedure and actively support corrective actions identified in Audits. Ensure compliance with Company Procedures and Work Practices pertinent to Construction activities. Ensure best available technology is implement on projects to align with the digitalisation of workflow processes. Develop in conjunction with the construction management function robust Equipment and Contract procurement strategies to enable successful project delivery. Enhance knowledge of supply chain across European Operations. Ensure project costs analysis are completed and cost database is up to date. Participate in the selection and approval of construction contractors appointed to undertake work for either the Company or on behalf of Clients. Ensure appropriate communication with the Project Management and Construction function occurs at all levels on all aspects of Project Controls. Participate in the recruitment of appropriate project controls resources. Mentor and invest in career development of project controls personnel. Project the Company’s image to clients, public and other third parties by ensuring effective liaison and harmonious relationships. Qualifications & Experience First and foremost, you share our passion for improving the quality of life. You pride yourself for the part you play in transforming the world around you and understand the importance of teamwork. You are a technically capable and come to us with: Degree Qualified Experience as Project Controls Manager on pharma projects of €100m+ Why Arcadis? At Arcadis, we empower everyone to be their best because your contribution matters. Shape your career, deliver sustainable solutions, and leave a lasting legacy. Our Commitment to Equality, Diversity, and Inclusion We’re dedicated to creating a workplace where everyone thrives. Through six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race—we foster innovation by embracing diverse perspectives. Join Arcadis DPS Group. Create a Legacy. #J-18808-Ljbffr
A leading engineering firm in Ireland is seeking a Senior Project Engineer to manage Oil & Gas assignments primarily located in Whitegate, Cork. The role entails leading small projects, overseeing site activities, and ensuring compliance with HSE standards. Candidates should have over 8 years of relevant experience and a degree in Chemical or Mechanical Engineering. This position offers a 12-month contract with opportunities for professional growth in a dynamic team environment. #J-18808-Ljbffr
Arcadis DPS Engineering are a seeking a Senior Project Engineer for an Oil & Gas assignment located in Whitegate, Cork. This is initially a 12-month contract. Responsibilities Lead and execute small projects from initiation to completion, ensuring delivery on time and within budget. Oversee and coordinate daily site activities, particularly in outdoor and challenging environments. Manage relationships and performance of contractors and vendors. Ensure compliance with all relevant HSE (Health, Safety & Environment) standards and company policies. Prepare and present detailed technical reports and project documentation. Identify and resolve project issues efficiently and practically. Communicate project status, risks, and recommendations to stakeholders and management. Support continuous improvement by identifying opportunities for process optimization. Requirements 8+ years in Oil & Gas, Chemicals, Power Generation, or similar heavy industry (offshore or onshore). Degree qualified Chemical or Mechanical Engineer. Excellent technical report writing and presentation abilities. Self-motivated, able to work unsupervised, practical, and resourceful. Strong verbal and written communication skills, adept at stakeholder engagement. 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
Senior Process Engineer – Dublin Arcadis is the world’s leading company in sustainable design, engineering, and consultancy for natural and built assets. With over 36,000 professionals in 70+ countries, we are united in improving quality of life and solving the world’s most complex challenges. About the Role Arcadis DPS Group specializes in Project Management, Multi-Discipline Design, and Construction Management for Pharmaceutical and Life Science Buildings. Based in our Dublin office, you will play a key role as Senior Process Engineer. Reporting to the Process Dept Manager, you will lead the development of production processes and drive plant improvements while providing technical expertise. Key Responsibilities Deliver Technical Excellence: take responsibility for process engineering deliverables sets—including PFDs, P&IDs, process reports, calculations, utility sizing, and equipment specifications—ensuring high standards of technical quality, safety, and compliance with project requirements, budgets, and schedules. Lead Project Sections: on smaller projects, lead the process engineering scope from design through to completion; on larger projects, manage specific sections or workstreams, supporting the Lead Process Engineer in achieving overall project goals. Manage Change and Controls: prepare, manage, and communicate process project change by assessing and implementing modifications to project scope, schedule, or budget; document all impacts, mitigate risks, and ensure project delivery commitments are maintained. Support & Mentor: provide guidance and support to junior engineers and team members, encouraging an environment of collaboration, continuous learning, and professional growth. Contribute to Project Delivery: collaborate with multidisciplinary teams, including other Arcadis offices, clients/end users, and equipment suppliers to coordinate and integrate process inputs and deliverables throughout the design process. Uphold Standards: ensure all work meets relevant local, international, and client-specific codes and standards. Drive Safety and Quality: participate in PHAs, HAZOPs, design reviews, and peer reviews, maintaining a strong focus on process safety and quality assurance. Engage with Clients: occasionally represent the process engineering team in client meetings or presentations, supporting the Lead Process Engineer as required. Innovate and Improve: identify opportunities for process improvement and support the implementation of new technologies and best practices within project teams. Skills & Experience Required Education: A higher technical degree in Industrial, Process, or Chemical Engineering. Experience: Minimum 7 years of experience as a process engineer in design consultancy or Food/Pharmaceuticals/GMP manufacturing environments, with demonstrated involvement in design project execution. Technical Skills: strong track record in process design, calculations, and documentation for engineering projects. Collaboration Skills: ability to work effectively across disciplines, with A&E teams, vendors, and system owners. Problem-Solving: solid decision-making and problem-solving abilities. Communication: strong written and verbal communication skills, with fluency in English. Teamwork: ability to work collaboratively within a team and to mentor junior colleagues. Tech-Savvy: proficiency in MS Office and process-related software, with good organisational and time-management skills. Nice-to-Have Pharmaceutical Industry SME: experience in process engineering design and implementation within the pharmaceutical sector, with the capability to serve as a Subject Matter Expert on projects. Leadership: experience managing small projects or leading sections within larger projects. Why Arcadis? At Arcadis, we empower everyone to be their best because your contribution matters. Shape your career, deliver sustainable solutions, and leave a lasting legacy. Our Commitment to Equality, Diversity, and Inclusion We’re dedicated to creating a workplace where everyone thrives. Through six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race—we foster innovation by embracing diverse perspectives. #J-18808-Ljbffr
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: Our client, a leading pharmaceutical company, is hiring an Automation Project Engineer to join their team in North Dublin. This role will lead the implementation of a BMS project on-site. It is a great opportunity for someone with strong project‑management ability and extensive experience with Siemens. The position is an initial 12‑month contract with a strong prospect for extension. Main Duties: Ensure the successful delivery of CapEx automation projects on site. Design, program, and implement automation solutions for manufacturing processes and systems. Participate in the IQ, OQ, PQ of relevant systems and equipment. Ensure that systems meet all relevant regulatory requirements. Prepare and review validation documentation, test protocols, design specifications, etc. Liaise with relevant internal and external stakeholders to ensure projects are completed on time and in adherence to scope and budget. Perform any other duties as required. Your background: Minimum 5 years’ experience in a similar position within the pharmaceutical or medical device sector working on BMS projects. Strong project‑management skills and experience with Siemens. 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. Seniority level Mid‑Senior level Employment type Full‑time Job function Pharmaceutical Manufacturing #J-18808-Ljbffr
A leading engineering consultancy in Dublin is seeking a Senior Process Engineer to lead process development and improvements. The ideal candidate will have over 7 years of experience in process engineering within the pharmaceutical sector. Key responsibilities include delivering engineering standards, managing project changes, and mentoring junior staff. This role offers opportunities for professional growth in a collaborative environment. #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
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
Process Engineer / Scientist We are seeking a Process Engineer / Scientist to join the Process Development Commercial Support team. This team is responsible for providing process and product support to drug product formulation and fill‑finish operations, acting as subject matter experts (SMEs) for all drug product processes. The successful candidate will provide technical and process support, lead investigations, and drive continuous improvement initiatives to optimise performance and ensure robust operations within a GMP environment. Key Responsibilities Primary Focus Areas: Provide day‑to‑day operational support as a subject matter expert in drug product formulation, vial filling, pre‑filled syringe filling, lyophilization, and vial capping . Serve as a key contributor to product and process investigations , including assessment of product and process impact. Lead continuous improvement projects aimed at enhancing process performance, yield, and productivity. Additional Responsibilities Include: Assess product impact associated with proposed process changes under the change control system. Generate product impact assessments for process deviations and excursions, referencing relevant product technical documentation. Support new product introductions (NPI) as a process SME – including recipe development, protocol execution, troubleshooting, and investigation support. Review and approve updates to operating procedures, electronic batch records, and product documentation. Conduct risk assessments and implement mitigation strategies related to equipment and line performance. Perform process gap analyses and develop strategies to address identified issues. Analyse process performance data and trends to identify and resolve potential issues. Basic Qualifications Bachelor’s or Master’s degree in Engineering, Science, or a related discipline , with a minimum of 6 years’ experience in a similar role; OR PhD with 3 years of directly related experience . Preferred Qualifications 4–6 years’ experience in drug product formulation, vial or pre‑filled syringe filling, or lyophilisation . Experience with new product introductions (NPI), process development, or MSAT in a GMP environment . Certification or demonstrated experience in Lean or Six Sigma methodologies. Strong analytical, problem‑solving, and communication skills. #J-18808-Ljbffr
