Direct message the job poster from DPS Group Global Senior Recruitment Specialist - Arcadis DPS Group | Pharma/Biopharma (Tech Transfer) | Oil & Gas Arcadis DPS Engineering are a seeking Project Engineer for a Pharmaceutical assignment located in Kinsale, Cork. This is initially a 12-month contract . The ideal candidate will have experience delivering medium-value projects in a GMP environment and will be responsible for overseeing projects from conception through to handover. Responsibilities: Manage and deliver medium-value projects (€1-2M range) within a GMP environment. Support the project lifecycle from concept through design, construction, commissioning, and handover. Interface with users and collaborate with multiple disciplines to ensure projects meet requirements, schedules, and budgets. Conduct risk assessments and develop mitigation strategies to ensure project success. Prepare and maintain project documentation, including design specifications, status reports, and close-out documentation. Ensure compliance with all relevant safety, quality, and regulatory standards. Coordinate and lead project meetings, providing regular updates to stakeholders. Identify and implement process improvements to enhance project delivery and efficiency. Requirements: Bachelor's degree in Mechanical or Process Engineering or a related field. Minimum of 5 years of experience in the pharmaceutical industry. Proven ability to deliver medium-value projects in a GMP environment. Strong independent work ethic and proactive problem-solving skills in a fast-paced manufacturing setting. Excellent communication and interpersonal skills, with the ability to interface effectively with diverse teams. DPS is a leading Project Management and Engineering Company delivering Full Service Engineering with a ‘client first’ mentality and personal touch across a range of market sectors: Project and Programme Management, Procurement, Design, Construction Management, Health & Safety Management, Commissioning, Qualification and Start-up. We have one goal: to deliver more than our clients expect first time, every time. We’ve been serving industry around the world for 40 years plus, relied on for our agility, original thinking, sound judgement and high-calibre people. What sets us apart is the rapport we build with our clients and the care we take to gain a fundamental understanding of our client’s businesses. We employ over 2800+ people out of our sixteen office locations and we serve a broad range of clients ranging from multinational companies to small generic producers. DPS Engineering is an Equal Opportunities Employer. Recruitment Agencies: Please do not reply to this job advert. Seniority level Seniority level Mid-Senior level Employment type Employment type Contract Job function Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at DPS Group Global by 2x Sign in to set job alerts for “Project Engineer” roles. Graduate Mechanical Engineer (Future Talent Opportunity) Cork, County Cork, Ireland €55,000.00-€70,000.00 21 hours ago Cork, County Cork, Ireland 32 minutes ago Mechanical Project Engineer – Asset Management - Utilities Project Engineer, Medical Device (12M, Cork) Mallow, County Cork, Ireland 3 months ago Cork, County Cork, Ireland €35,000.00-€35,000.00 2 weeks ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
Arcadis DPS are seeking a Mechanical Utilities Engineer on a 12-month rolling contract basis for a leading Biopharma company in Sligo. Responsibilities: To manage the execution of projects within the group. To carry out and implement equipment and process improvement initiatives. To ensure the performance of day-to-day preventative and demand maintenance activity for manufacturing and utility equipment. Establish with the Site Engineering Services Manager the performance goals, schedules and timetables for activities Assist with the management and supporting of manufacturing / utility / facility project plans. Preparation of capital expenditure requests for the facility, plant and equipment. Develops monthly engineering metrics for operations, utilities, and facilities which includes owner ship of Site Maintenance Excellence Program to drive operational improvements including implementing cost savings and capex budget management. Ensure successful agency, external, divisional and corporate audits as relates to engineering compliance systems. Issue management reports as requested and on time. Cross train within department to ensure appropriate preventive maintenance schedules are achieved. Ensure safety Quality, Engineering & Safety standards are met Implementation of equipment/process upgrades in an environment of continuous improvement. Support the Engineering Team in ensuring that manufacturing equipment is maintained to meet the required legal, divisional and corporate standards. Liaise with Global Engineering as required. Ensure the effective management of appropriate internal and external plant projects. Supervise external contractors which include development of performance metrics for third party service providers of site services. Negotiate cost and drive quality & performance with external contractors. Prepare appropriate CAPA plans and implement timelines. Requirements: Bachelor’s Degree: Engineering (Mechanical, Chemical, Electrical, Biomedical, Electronics) or Relevant Discipline 5+ years’ experience in Facility and Utility Engineering, preferably in a cGMP environment. It may be necessary to re-design elements of manufacturing / utility / facility machinery to adapt to process conditions to improve efficiency with a demonstrated track record in managing budgets. Experience in Chilled Water, boilers, Potable Water distribution, Compressed Air Generation, LPHW, Building Management Systems, Environmental Management Systems, Electricity, Building Safety Systems and Building regulations is desirable. Interested parties should apply via the link below or contact Fergal Walshe via LinkedIn for more information regarding the opportunity #J-18808-Ljbffr
Arcadis DPS Engineering are a seeking a Clinical Supplies Qualified Person (QP) for a Pharmaceutical assignment located in Ballydine, Tipperary. This is an 11-month contract. Responsibilities: Review and certify batches intended for use in clinical trials to ensure compliance with EU GMP, the Product Specification File, and the Clinical Trial Application. Oversee batch certification for products manufactured globally and imported into the EU, including small molecules, biologics, vaccines, and gene therapies. Participate in Health Authority inspections and audits to maintain site licences and ensure compliance. Manage ongoing compliance activities related to clinical trials, including technical and quality agreements with collaborators. Coordinate with cross-functional teams to ensure clinical trial supplies meet quality and regulatory standards. Provide expertise on EU regulations, including EudraLex Chapter 4, Annex 13, Annex 16, and EU CTR regulations 536/2014. Act as a key contact for quality-related issues, ensuring timely resolution and adherence to standards. Support the implementation of process improvements to enhance compliance and efficiency in clinical trial supply management. Requirements: Eligibility to be named as a Qualified Person (QP), with a commitment to maintaining CPD. Practical experience with product disposition, including sterile, non-sterile, biologics, vaccines, or gene therapy, and at least two years in quality assurance or qualitative analysis. Recognised pharmacy degree or equivalent Extensive experience in a cGMP environment, preferably within a Quality function for clinical trials or IMPs. Strong organizational and communication skills, with a proactive approach to working on global teams and collaborating with internal and external stakeholders. DPS is a leading Project Management and Engineering Company delivering Full Service Engineering with a ‘client first’ mentality and personal touch across a range of market sectors: Project and Programme Management, Procurement, Design, Construction Management, Health & Safety Management, Commissioning, Qualification and Start-up. We have one goal: to deliver more than our clients expect first time, every time. We’ve been serving industry around the world for 40 years plus, relied on for our agility, original thinking, sound judgement and high-calibre people. What sets us apart is the rapport we build with our clients and the care we take to gain a fundamental understanding of our client’s businesses. We employ over 2800+ people out of our sixteen office locations and we serve a broad range of clients ranging from multinational companies to small generic producers. DPS Engineering is an Equal Opportunities Employer. Recruitment Agencies: Please do not reply to this job advert. #J-18808-Ljbffr
Arcadis DPS are seeking a Filling Line Projects Engineer on an hourly rate contract basis for a leading Biopharma company in Sligo Responsibilities: To work as a team member to support engineering in pharma operations in line with all safety, regulatory and organizational requirements. Develop and modify procedures as needed to support the manufacturing operation. Participate in process, equipment, and facilities validations efforts and projects implementations. Process and equipment engineering Subject Matter Expert for a vial filling and isolator equipment from design phase to equipment handover. Review, and approve process flow diagrams (PFDs), specifications, layouts and P&ID’s. Interface with vendor to ensure that equipment/facility designs are aligned and to ensure efficient transfer of information between vendor and site. Review vendor design documentation to ensure compliance with process and technical specifications. Lead the FAT and SAT activities ensuring the equipment is design, fabricated and tested to meet the technical requirements of the project. Support foller equipment installation integration and co-ordinate vendor supervision as required. Support the development of the project commissioning and validation plan. Develop commissioning plans for all process related equipment ensuring that plans meet the requirements of Good Engineering Practice (GEP) Review all process related validation protocols for completeness and accuracy. Execute protocols in a timely basis to meet the project schedule requirements. Participating in design and process project conversations to ensure reliability by design is built in prior to equipment arrival. Leadership of manufacturing and validation activities during project life cycle. Support of technical transfers for future product introductions to the site. Assesses and owns the relationship between process requirements and unit operation equipment. Understands the impact of equipment control systems on processing performance Investigate process exceptions or equipment malfunction incidents affecting the process. Liaising with operations, quality and S&T to ensure equipment and process performance is maximized. To liaise with Internal/External Engineering Personnel and contract maintenance providers in maintaining trouble shooting and installing/commissioning equipment. Implementation of equipment/process upgrade in an environment of continuous improvement. Support the Production Team in ensuring that manufacturing equipment is maintained to meet the output and yield requirements. Adhering to all relevant policies relating to Quality & Safety. Ensure successful external inspections, and Division and Corporate audits. Supervision of external contractors. Requirements: A relevant third level qualification in an engineering, science or technical discipline (Degree Level or Masters Preferable) At least six (5) years of total combined experience in Process / Equipment or Manufacturing Engineering of a Pharmaceutical and Health Care Organization. At least three (3) years of experience in the manufacturing environment of a biotechnology, pharmaceutical or health care plant. Previous experience in manufacturing processes of biotechnological drugs, parenteral drugs, solutions preparation, and sterilization operations preferable. Experience in new product introductions (drug product) to pharmaceutical facilities is desirable Interested parties should apply via the link below or contact Fergal Walshe via LinkedIn for more information #J-18808-Ljbffr
1 day ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Direct message the job poster from DPS Group Global Arcadis DPS : Life Science Engineering Experts! Arcadis are seeking a Qualified Person on a contract basis for a biotech facility in Sligo Responsibilities: Comply with EudraLex Volume 4 EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use Annex 16: Certification by a Qualified Person and Batch Release; Article 47 of Directive 2001/83/EC. Qualified Person is responsible for ensuring that each individual batch has been manufactured and checked in compliance with laws in force in the Member State where certification takes place, in accordance with the requirements of the Product Specification File (PSF)/Marketing Authorisation (MA) and with Good Manufacturing Practice (GMP) for products manufactured at the biologics facility in Sligo To ensure that products manufactured are manufactured in accordance with the relevant GMPs. The Quality Assurance Specialist / Qualified Person (QP) is responsible for the disposition of bulk product manufactured at site as acceptable for release or reject based on the information available relating to the manufacture and testing of the product. To disposition bulk product as acceptable for release, or reject, to ensure patient safety based on the information available relating to the manufacture and testing of the batch. Requirements: Third level qualification in a science discipline with 5 years' experience in the pharmaceutical industry. MSc in Industrial Pharmaceutical Science or similar course recognized by Regulatory Authority to permit Qualified Person (QP) status as per Article 49 of Directive 2001/83/EC 5 years industrial experience gained in an FDA and EMEA approved pharmaceutical environment. 2 Years’ experience gained within an aseptic processing environment, ideally gained within a quality function. Interested parties should forward a copy of their CV through the link below or contact Fergal Walshe via LinkedIn for more information regarding the opportunity Seniority level Seniority level Not Applicable Employment type Employment type Contract Job function Job function Quality Assurance and Manufacturing Industries Pharmaceutical Manufacturing and Biotechnology Research Referrals increase your chances of interviewing at DPS Group Global by 2x Get notified about new Quality Assurance Manager jobs in Sligo, County Sligo, Ireland . We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
Get AI-powered advice on this job and more exclusive features. Direct message the job poster from DPS Group Global Recruitment Specialist @ Arcadis DPS Group Job Purpose: Dublin based Oral Solid Dose Pharmaceutical client require a Senior Project Engineer for their Capital Projects Group. They will also manage the delivery of the key documentation required for a best-practice Stage Gate managed process, including (but not limited to) a detailed Project Execution Plan and cost estimate. They will manage the full range of activities associated with the project life-cycle from cradle to grave: URS; Concept; Basis of Design; Detailed Design; Construction; Commissioning and Qualification. Responsibilities: Project management and coordination of same within the production environment. Installation, Commissioning, and Validation of manufacturing plant equipment and processes. Troubleshooting and debug of equipment under the site change control system. Leading the generation of lifecycle documentation for process equipment and associated systems.(URS, FDS, DDS, FAT, SAT, IQ/OQ, Risk Assessments, procedures etc). Supporting Engineering functions, such as Factory Acceptance Testing, Commissioning, Qualification, etc. applying good project management and Engineering principles. Ensuring Projects are handed over in a controlled manner with manuals, training maintenance systems and site master drawings updated. Optimisation of new and existing processes to achieve production output targets. Provide routine technical support for assigned process and packaging activities. Review line metrics and provide technical solutions to increase operational efficiency. Collaborate significantly with internal/external functions and suppliers to finalize process and equipment design. Follow cGMP guidelines, safety procedures, and SOPs at all times. The Person/Requirement The successful applicant must possess the following knowledge, skills, qualifications and experience. A 3rd level Engineering (honours) degree in a relevant field of study. E.G Mechanical, Process or Chemical Engineering (other disciplines may also be considered) 5+ Years experience in Pharmaceutical Project Engineering with OSD experience an advantage Significant exposure to Technical Investigations and Process Optimisation initiatives and projects. Excellent time management skills with ability to prioritise and work to strict deadlines. Excellent leadership (Projects), interpersonal, presentation and communications skills with the ability to work within cross-functional teams. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Project Management and Engineering Industries Pharmaceutical Manufacturing, Biotechnology Research, and Engineering Services Referrals increase your chances of interviewing at DPS Group Global by 2x Get notified about new Project Engineer jobs in Dublin, County Dublin, Ireland . Dublin, County Dublin, Ireland 3 weeks ago Dublin, County Dublin, Ireland 1 month ago Dublin, County Dublin, Ireland 2 days ago Dublin, County Dublin, Ireland 2 weeks ago Dublin 14, County Dublin, Ireland 1 day ago Dublin, County Dublin, Ireland 2 weeks ago Dublin 14, County Dublin, Ireland 1 day ago Dublin, County Dublin, Ireland 1 week ago Dublin, County Dublin, Ireland 2 weeks ago Dublin, County Dublin, Ireland 1 month ago Engineering Graduate Rotation Programme 2025 – Damastown Dublin, County Dublin, Ireland 1 week ago Dublin, County Dublin, Ireland 3 weeks ago Dublin, County Dublin, Ireland 1 month ago Dublin, County Dublin, Ireland 2 weeks ago Dublin, County Dublin, Ireland €73,000.00-€87,500.00 2 weeks ago Dublin, County Dublin, Ireland €72,000.00-€85,000.00 2 weeks ago Dublin, County Dublin, Ireland 2 weeks ago Dublin, County Dublin, Ireland 2 weeks ago Maynooth, County Kildare, Ireland 1 week ago Dublin, County Dublin, Ireland 1 week ago Dublin, County Dublin, Ireland 4 days ago Dublin, County Dublin, Ireland 3 weeks ago Dublin, County Dublin, Ireland 2 days ago Dublin, County Dublin, Ireland 2 months ago Dublin, County Dublin, Ireland 1 week ago Mechanical Project Engineers - Dublin - 144386 Dublin, County Dublin, Ireland 1 week ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
DPS Engineering are a seeking a Senior Project Manager for a Pharmaceutical assignment located in Ringaskiddy, Cork. This is initially a 12 month contract. Responsibilities: Lead and manage a €7 million project from inception to completion, ensuring all objectives are met on time and within budget. Develop comprehensive project plans, including timelines, resource allocation, and risk management strategies. Collaborate effectively with internal teams and external partners to ensure seamless communication and alignment on project goals. Ensure all project deliverables meet the highest standards of quality and compliance with industry regulations. Track project progress and performance, implementing corrective actions as needed to maintain project trajectory. Optimize the use of project resources, including personnel, materials, and budget, to maximize efficiency and effectiveness. Prepare detailed project reports for senior management, highlighting key milestones, challenges, and opportunities. Identify opportunities for process improvements and implement best practices to enhance project delivery. Requirements: Bachelor’s Degree in Project Management, Engineering, or a related field. Proven experience at a similar level in project management, ideally within the pharmaceutical sector. In-depth knowledge of the pharmaceutical industry, including regulatory requirements and industry best practices. Must be eligible to work in Ireland. Demonstrated ability to lead cross-functional teams and manage complex projects successfully. DPS is a leading Project Management and Engineering Company delivering Full Service Engineering with a ‘client first’ mentality and personal touch across a range of market sectors: Project and Programme Management, Procurement, Design, Construction Management, Health & Safety Management, Commissioning, Qualification and Start-up. We have one goal: to deliver more than our clients expect first time, every time. We’ve been serving industry around the world for 40 years plus, relied on for our agility, original thinking, sound judgement and high-calibre people. What sets us apart is the rapport we build with our clients and the care we take to gain a fundamental understanding of our client’s businesses. We employ over 2400+ people out of our 17 office locations and we serve a broad range of clients ranging from multinational companies to small generic producers. DPS Engineering is an Equal Opportunities Employer. Recruitment Agencies: Please do not reply to this job advert. #J-18808-Ljbffr
Project Controls Department Manager Dublin Arcadis is the world’s leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets. We are more than 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 solve the world’s most complex challenges and deliver more impact together. Role Description The Project Controls Department Manager will be a key role within the Operations leadership team. The role will involve the delivery of the following Project Controls areas across all projects within the operation: Project reporting & control of indirect cost Project Change Management Project Planning and scheduling Project cost estimating Equipment and Contract Procurement Contract Administration The role will involve working closely with Clients, Business/Operations Director, Project Managers, Engineering Discipline Managers, and Construction Management Teams. Reporting Lines The Project Controls Department Manager will report to the Business/Operations Director. Duties & Responsibilities: Successful delivery of Project Controls function across all projects. Preparation of Project Controls Proposals and associated ProServices hours estimates. Supporting Business Development and participation in presentations. Resourcing Project Controls teams in line with agreed staffing plans. Ensure best available technology is implemented on projects to align with the digitalisation of workflow processes. 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 technically capable and come to us with: Degree Qualified. Experience as Project Controls Manager on Industrial projects of 100m+. Ability to convey complex information clearly to diverse stakeholders. Strong analytical capabilities to assess project performance, identify trends, and implement corrective actions. Continue Your Career Journey as an Arcadian We can only achieve our goals when everyone is empowered to be their best. We believe everyone’s contribution matters. It’s why we are pioneering a skills-based approach, where you can harness your unique experience and expertise to carve your career path and maximize the impact we can make together. You do meaningful work, and no matter where your next role in Arcadis takes you, you’ll be helping to deliver sustainable solutions for a more prosperous planet. Make your mark; on your career, your colleagues, your clients, your life, and the world around you. Together, we can create a lasting legacy. Our Commitment to Equality, Diversity, Inclusion & Belonging: We want you to be able to bring your best self to work every day which is why we take equality and inclusion seriously and hold ourselves to account for our actions. Our ambition is to be an employer of choice and provide a great place to work for all our people. We believe that by working together diverse people with different experiences develop the most innovative ideas. Equality, diversity, and inclusion is at the heart of how we improve quality of life and we work closely with our people across six ED&I Workstreams: Age, Disability, Faith, Gender, LGBT+ and Race. A diverse and skilled workforce is essential to our success. #LI-TY1 #J-18808-Ljbffr
Senior Architect SME About Us As an Arcadian, you help 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. Position Summary The ideal candidate will have experience in a team environment, experience running and designing enterprise-scale services and platforms, technical depth in cloud platforms, agile development practices, and experience in designing & tuning telemetry. In addition, this position requires an individual who can demonstrate the ability to ensure highly resilient and scalable service designs through partnership with other members of the service team. Job Description: The datacenter design architect will be responsible for the development of Microsoft’s industry-leading datacenter designs which includes defining new technology and advanced concepts from pre-programming through design development, construction, and the turnover to Operations. Key Responsibilities: This position will manage multiple projects on a global scale and be part of the core team that’s launching the Microsoft cloud. The Design Architect will provide thought leadership and direction for the civil, structural, and architectural workings to align with defined project scope, schedule, and budget. The architect will engage with key MS stakeholders, authority having jurisdiction, as well as outside vendors who specialize in datacenter architecture. The candidate will provide technical direction to vendors which includes professional architects, civil and structural engineers. This position will manage multiple concurrent projects on a global scale and be part of the core team that’s launching the MS cloud infrastructure worldwide. Some domestic and international travel is required. The architect will provide technical direction for the civil, structural, and architectural components of the projects including facilitating systems coordination and organization throughout the sites and datacenters. The candidate must have excellent communication, be highly organized and exhibit a high level of project leadership; possess a high level of expertise in commercial and industrial architecture with a primary focus on datacenter design; have adequate experience in civil and structural design to provide confident direction to civil and structural engineering vendor experts. The candidate must also be able to work with other technical and non-technical groups in a fast-paced environment and must be a person of integrity with a methodical and detail-oriented work ethic. Knowledge, Experience, and Skills: Bachelor’s degree in Architecture Registered Professional Architect 10+ years of experience in architecture/engineering with experience as a lead architect 7+ years of experience in mission-critical projects (Datacenters, Laboratories, and/or Micro-Electronics projects or similar) Demonstrated ability to write, speak, and present information effectively and persuasively Excellent analytical and organizational skills Strong interpersonal skills; ability to lead and be proactive Excellent problem-solving, judgment, team building, and decision-making skills Experience using MS Outlook, Word, PowerPoint, MS Project, Visio, and Excel including effective reporting/presentations of project information Preferred, Not Required: Experience operating CAD, Sketchup and/or BIM software for drawing review and adjustments is desirable #J-18808-Ljbffr
Design Safety Lead 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 Cork office, you will lead design safety for diverse Pharmaceutical and Life Science projects across Ireland and Europe, reporting to our Design Safety Manager. Be part of something impactful – join us! Key Responsibilities: Design Safety Coordination: Act as the primary Health & Safety Coordinator during the design phase (PSDP role). Conduct detailed reviews of safety-related documentation (e.g., Hazardous Area Classifications, Risk Assessments, and Emergency Relief Calculations). Oversee and maintain Design Safety documentation (e.g., Basis of Safety, Preliminary Health & Safety Plan). Lead and document multidisciplinary Risk Assessment exercises, including HAZID/HAZOP/LOPA. Coordinate action closures from risk assessments and ensure project Safety File handover. Client & Team Support: Support business development and maintain client relationships. Ensure adherence to Arcadis General Business Principles, codes, and standards. Experience & Skills Required: Engineering qualification (Third Level) with 10+ years in a multi-disciplinary design office or client engineering team. Background in Design or Process Safety (PSDP experience desirable). Familiarity with designing Active Pharmaceutical Ingredient (API) manufacturing facilities is an advantage. Strong interpersonal, communication, organizational, and multitasking skills. Detail-oriented, self-motivated, and capable of working independently. Why Arcadis? At Arcadis, we empower everyone to be their best because your contribution matters. We take a skills-based approach, allowing you to shape your career and maximize your impact. By joining us, you’ll do meaningful work, delivering sustainable solutions for a better planet and leaving a lasting legacy. Our Commitment to Equality, Diversity, and Inclusion We’re dedicated to creating a workplace where everyone can thrive. Through six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race—we foster innovation by bringing together diverse perspectives. Together, we improve quality of life while building a more inclusive future. Join Arcadis. Create a Legacy. #ARCTY #LI-TY1 #J-18808-Ljbffr
