Senior Project Planner

Senior Project Manager - Netherlands, Nijmegen - Long Term Contract/ Permanent PositionQCS Staffing are partnered with a leading independent company who combine engineering, design and consultancy services with software and technology to deliver complex projects across the globe. Our client’s projects include those in the Data Center, Pharmaceutical, Manufacturing, FMCG, Infrastructure, Transport and Water sectors to name a few. Their team is composed of experts in diverse fields such as electrical engineering, mechanical engineering, construction, civil engineering, structural engineering, architecture, fire safety, control engineering, security technology and project management to name a few.To support with these projects and their continued growth, they are currently looking to hire a Senior Project Manager in the Netherlands.What you’ll do: Lead and manage design projects from inception to completion, ensuring they are delivered on time, within scope, and within budget.Develop and maintain project plans, schedules, and budgets.Coordinate and communicate with clients, stakeholders, and team members to ensure project requirements are understood and met.Oversee the design process, ensuring that all design work meets the highest standards of quality and creativity.Identify and mitigate project risks and issues. What you’ll need: Bachelor’s degree in an Engineering related field (Mechanical, Electrical, Civil, Structural etc).Extensive experience in project management, with a focus on design projects.Strong engineering background, preferably with experience as a Design Engineer.Previous employment by a design and engineering company.Strong knowledge of project management methodologies and tools. If this role is of interest to you, please apply now!#LI-LG1

Senior Project Manager - Switzerland, Zurich - Permanent ContractQCS Staffing are partnered with a leading independent company who combine engineering, design and consultancy services with software and technology to deliver complex projects across the globe. Our client’s projects include those in the Data Centre, Pharmaceutical, Manufacturing, FMCG, Infrastructure, Transport and Water sectors to name a few. Their team is composed of experts in diverse fields such as electrical engineering, mechanical engineering, construction, civil engineering, structural engineering, architecture, fire safety, control engineering, security technology and project management to name a few.To support with these projects and their continued growth, they are currently looking to hire a Senior Project Manager in Zurich.What you’ll do: Lead and manage design projects from inception to completion, ensuring they are delivered on time, within scope, and within budget.Develop and maintain project plans, schedules, and budgets.Coordinate and communicate with clients, stakeholders, and team members to ensure project requirements are understood and met.Oversee the design process, ensuring that all design work meets the highest standards of quality and creativity. What you’ll need: Bachelor’s degree in an Engineering related field (Mechanical, Electrical, Civil, Structural etc). Extensive experience in project management, with a focus on design projects.Strong engineering background, preferably with experience as a Design Engineer.Previous employment by a design and engineering company. If this role is of interest to you, please apply now! #LI-ID1

CQV Owners Representative - Copenhagen - 12 Month ContractOur client, a global pharmaceutical company, are looking for a CQV Owners Representative to join their team. The company has grown to become a world leader in the development, manufacture, and marketing of innovative pharmaceutical products to alleviate some of the world’s biggest health problems. What you'll do: Work as Owners rep witnessing CQV contractor, people with enough knowledge to spot when something is wrong and know how to work within a project to get this rectified, ensuring CQV contractor delivers to scope1 Utilities and 1-2 Recovery/Clean Utility focusedEnsure that Commissioning, Qualification, and Validation (CQV) activities meet project and regulatory requirements. What you'll need: Must have experience managing large construction projects (500mn )Client-side experience is preferredStrong experience and proof having worked in a similar role/project. If you would like to apply or find out more, get in touch now!#LI-SC1

HVAC Lead - Denmark, Copenhagen - 12 Months Initial ContractOur client, a global pharmaceutical company, are looking for a HVAC Lead to join their team. The company has grown to become a world leader in the development, manufacture, and marketing of innovative pharmaceutical products to alleviate some of the world’s biggest health problems. What you'll do: Work alongside the EPCM/V and provide direction on areas that can be exploited. The site is huge and they need to help improve the delivery of the EPCM/VIdentifying opportunities to improve scheduleEnsure EPCM/V progress reporting is accurate and if not ensure this is resolvedEnsuring EPCM/V are allocating enough bodies into right areas to achieve required progress What you'll need: A strong background on previous project work in the Pharmaceutical IndustryRobust personalities who can strongly and confidently manage the EPCM/VStrong HVAC experience. If you would like to apply or find out more, get in touch now!#LI-JS5

Rigger - Cologne, Germany - 6 Month ContractAre you looking for your next short-term contract Rigger assignment? Our client, a global leader in crane rental services, is looking to onboard a talented UK based Offshore Crane operator for an ongoing offshore construction project. With state-of-the-art equipment and value engineering, this is your chance to join our client in their creative and intelligent solutions to support this major project. The scope of this construction project is to transport, lift and install various offshore components. What you’ll do: Rigger & Banksman workPreparation works for executing load in lifts with Heavy lift crawler cranes and mobile cranes.Banksman for executing lifts with crawler cranes and mobile cranes What you’ll need: Passport or ID cardDriving licenseA1Basic safety certificate (VCA or equivalent)Certificate of medical examination (fit-to-work certificate)Rigging certificateGWO – Working at heightsWorking with telehandlerCommunicative in English If this role is of interest, please apply now. #LI-CT2

Project Manager - Ireland, Arklow - 12 Month Contract Are you local to Arklow and looking for your next contract assignment? Our client, a leading pharmaceutical organisation, are recruiting for a Project Manager to join their newly assembled team and help contribute towards the development of their next core projects.   What you'll do: Build relationships with the site teams, manage the projects, and execute improvement initiatives to drive growthDrive projects to ensure complianceMaintaining working with appropriate stakeholders (QA, Maintenance, Capital) to improve unit efficiency and performanceDevelops a knowledge and understanding of products/systems/services, customers and customer needs of business area supported.Conducts feasibility studies, determines manpower and cost estimates, and develops engineering criteria. What you'll need: Primary Degree in Mechanical / Process / Chemical / Electrical EngineeringExtensive Project Experience with knowledge and exposure to Process Plant, Utilities, Electrical, Maintenance & Facilities systems and ideally within a highly regulated GMP environmentUnderstanding of GMP and the Quality standards required in the Pharmaceutical Manufacturing sectorAPI Previous experience ideally If this role is of interest to you, please apply now!#LI-FY1

Lab CSV Engineer - Dublin, Ireland - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Lab CSV Engineer for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology. What you’ll do: Develop and execute validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), for computer systems and software applications.Collaborate with cross-functional teams, including IT, Quality Assurance, and Operations, to ensure compliance with regulatory guidelines and internal policies.Perform risk assessments and impact analyses to identify critical system functionalities and potential vulnerabilities.Create and maintain validation documentation, such as validation plans, test scripts, traceability matrices, and validation summary reports.Conduct periodic reviews to ensure ongoing compliance with regulatory requirements and internal procedures. What you’ll need: Bachelor's degree in Computer Science, Engineering, or a related field.Experienced in computer systems validation (CSV) from requirements to through release of analytical instruments used in Quality Control (QC) laboratories or in manufacturing operations as part of Process analytical Technology (PAT).Experienced in computer systems validation (CSV) of server / database-based laboratory software, middleware and enterprise applications, for example LIMS, Empower, NuGenesis.Completion of Electronic Record Electronic Signatures (ERES) assessments and Data Integrity Risk Assessments for analytical instruments and software systems.Experienced in the use of paperless validation and test tools such as ValGenesis, Kneat, ALM.  If this role is of interest, please apply now!#LI-JS4

CQV Engineer Benchtop Equipment - Dublin, Ireland - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a Benchtop Equipment CQV Engineer for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology. What you’ll do: Development and execution of CQV testing documentation for benchtop, mobile, analytical, PAT, incubators, BSCs, and TCU equipment for the Sterile Drug product facility.Responsible for meeting key project deliverables for safety, CQV schedule and quality of project related documentation/electronic records for equipment, utilities assigned.Responsible for ensuring GMP equipment are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.Responsible for ensuring that all equipment, is tested in compliance with project related standards from a commissioning perspective.Deviation management associated with the assigned equipment and utilities. What you’ll need: The ideal candidate should hold a minimum of a BS qualification (Degree) in a scientific, technical or engineering disciplineExtensive experience within the pharmaceutical industrial ideally with familiarity with Sterile Drug Product filling line experience.Demonstratable capacity to effectively execute the CQV testing approach for assigned from initiation to completion.CQV project lifecycle experience from design through to C&Q and handover.Demonstrable experience of performing as part of diverse team of CQV professionals/ contractors to deliver on tasks safely, with quality focus, on time and within budget. If this role is of interest, please apply now!#LI-JS4

CQV Engineer - Formulation & Component Prep - Dublin, Ireland - 12 Month ContractOne of the top 10 best companies to work in Ireland is looking for a CQV Engineer for their large-scale new facility in Dublin. Is this you? An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology. What you’ll do: Development and execution of CQV testing documentation for Equipment for the Sterile Drug product facility.Responsible for meeting key project deliverables for safety, CQV schedule and quality of project related documentation/electronic records for equipment assigned.Responsible for ensuring GMP equipment are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.Responsible for ensuring that all non GMP equipment, are tested in compliance with project related standards from a commissioning perspective.Deviation management associated with the assigned equipment and utilities. What you’ll need: The ideal candidate should hold a minimum of a BS qualification (Degree) in a scientific, technical or engineering disciplineExtensive experience within the pharmaceutical industrial ideally with familiarity with Sterile Drug Product filling line experience.Demonstratable capacity to effectively execute the CQV testing approach for assigned from initiation to completion.CQV project lifecycle experience from design through to C&Q and handover.Demonstrable experience of performing as part of diverse team of CQV professionals/ contractors to deliver on tasks safely, with quality focus, on time and within budget. If this role is of interest, please apply now!#LI-JS4