CQV Engineer The Commissioning, Qualification, Validation resource will report to the Commissioning / Qualification/ Validation lead. The person will be responsible for the successful Preparation of protocols and completion of commissioning and qualification activities on dedicated systems. The Commissioning, Qualification, Validation resource will report to the Commissioning / Qualification/ Validation lead. The person will be responsible for the successful Preparation of protocols and completion of commissioning and qualification activities on dedicated systems.

Process Engineer Position summary: We are currently hiring Process Engineers for our Dublin office. Applicants should have between 2-7 years’ experience. Successful applicants will work closely with colleagues in the process group and other DPS departments to deliver projects for our clients. Our clients are primarily in the Pharmaceutical, Life Science and Food and Beverage sectors. DPS provides full EPCMV (Engineering, Procurement, Construction Management and Validation) services for its clients.

Senior CQV Engineer required for Pharmaceutical client

Process Engineers required for long term opportunity with Dublin based Pharmaceutical client

DPS are seeking a Full Stack Developer for our Advanced Technology Group (ATG team)

DPS are seeking a Senior Business Analyst for our Advanced Technology Group

DPS are seeking an IT Development - Project Manager for our Advanced Technology Group (ATG)

Construction Manager required for DPS Project team based onsite in Co Wicklow

Electrical Site Supervisor required for DPS Project Team based onsite in Co Wicklow

Mechanical Site Supervisor required for DPS Project Team based onsite in Co Wicklow

DPS is seeking a talented and energetic Talent Acquisition Specialist who will serve as the primary point of contact as it pertains to management of staff augmentation services. He/she will be responsible for full lifecycle recruitment from candidate engagement to placement by developing and maintaining the relationship with the Client and Candidates through best in class augmentations services.

DPS is seeking a knowledgeable Quality professional to work with a pharmaceutical client in the Boston, MA area. This individual would be expected to take over the development of an FDA inspection readiness program and help the client to improve their current SOPs and systems to build a more robust inspection readiness plan and procedure. The ideal candidate would own this scope of work and lead the way to implement facility improvements, SOPs and plans with the ability to offer suggestions to the client on industry best practices and policies.

DPS has an excellent opportunity for a highly motivated and ambitious Technical Recruiter to work out of our multidiscipline Engineering Design office in Framingham, MA. As a Technical Recruiter, the successful candidate will support our US Staff Augmentation Business. Reporting to the Vice President of Resourcing, the Technical Recruiter will be responsible for developing, and expanding our business in the USA. Our main clients are currently based on the East Coast and DPS strategy is to build both the existing business in this region and expand throughout the USA. To succeed in this position the candidate must have a strong background in Technical Recruitment supporting Engineering Life sciences and or Microelectronics.

Support the safety planning process for contractor activities. Provides oversight of contractor field activities as required to ensure compliance with EHS requirements.

The Functional area construction coordinator will supervise and coordinate the activities for the tools under their ownership. The CC’s will report to the Project Manager and will take responsibility for implementation of the plans developed by the Project Manager. TI Construction Coordinator (“CC”) is focal point of all trade activities for the respective Functional area (“FA”) or Tool install area

DPS is currently hiring a Lead Process engineer / Department Manager for our Dublin office. We are seeking a senior process engineer with leadership capabilities and extensive experience in the pharmaceutical/Bio engineering project delivery. A key skill/knowledge in process safety is mandatory.

The EHS Specialist will ensure the organisation meets all regulatory and corporate requirements from an EHS & Risk Management perspective, coordinating and implementing all assigned OH&S tasks related to EHS objectives and activities on site.

DPS is currently seeking a Structural Engineer to join our multi-disciplined team working on exciting projects for 1 of our client . Are you an Structural Engineer, capable of undertaking tasks independently on a project? You ideally have experience of working on the entire design process (Basic of design, Detailed design, Construction Support) with between 5 and 7 years experience. Are you looking for a career opportunity with growth potential in a dynamic and international environment?

DPS is currently hiring a Process engineer for one of our clients. Are you a process engineer with experience in the chemical market with a passion for the development of production processes? Are you looking for a dynamic and international work environment? Please find details below.

DPS is seeking an established and knowledgeable Senior CQV Project Manager to work with a BioPharma client in the Southern NH area. Ideal candidates should have previous experience devising and implementing process and equipment validation strategy and authoring site validation master plans within cGMP capital project settings.

DPS is seeking a Senior Process Engineer to support our Framingham, MA office location. This position is a part of a larger team that provides Process Engineering support to Biotech and Pharmaceutical manufacturers that are designing facilities for new clinical candidates and existing products. Applicants should have between 8+ years’ experience, preferably in support of cGMP processes or design. Successful applicants will work closely with colleagues in the process group and other DPS departments to deliver projects for our clients. Our clients are primarily in the Pharmaceutical, Life Science and Food and Beverage sectors. DPS provides full EPCMV (Engineering, Procurement, Construction Management and Validation) services for its clients.

DPS is seeking a Junior Process Engineer to support our Framingham, MA office location. This position is a part of a larger team that provides Process Engineering support to Biotech and Pharmaceutical manufacturers that are designing facilities for new clinical candidates and existing products. Applicants should have between 1-7 years’ experience. Successful applicants will work closely with colleagues in the process group and other DPS departments to deliver projects for our clients. Our clients are primarily in the Pharmaceutical, Life Science and Food and Beverage sectors. DPS provides full EPCMV (Engineering, Procurement, Construction Management and Validation) services for its clients.

DPS is seeking a Construction Project Manager to support our Framingham, MA office location. The Project Manager manages key client projects within the Construction Management Department. Projects will include both those designed by other parties and design/build projects for which the PM will manage the design portion of the project as well as the execution. Project management responsibilities include the coordination and completion of projects on time within budget and within scope. Oversee all aspects of projects. Set deadlines, assign responsibilities and monitor and summarize progress of project. Prepare reports for upper management and clients regarding status of project. The successful candidate will work directly with clients to ensure deliverables fall within the applicable scope and budget. He or she will coordinate with other departments to ensure all aspects of each project full fill client needs while adhering to DPS standards of care.

DPS is looking for a proven Document Control Specialist to assist with a BioPharma client in the Cambridge, MA area. The ideal candidate should have previous experience working within a GMP environment and have familiarity with Quality Management Systems.

DPS Engineering is looking for a Facilities resource to work with a BioPharma client in the Greater Boston, MA area. This individual will provide Project Management and support to Facility-related Projects and must have a strong understanding of GMP manufacturing environments.

DPS Group Global is momenteel op zoek naar een Projectleider.

DPS Group Global is currently looking for a Pharmaceutical Scientist. The Pharmaceuticals Division helps treat some of the most pervasive and persistent health conditions around the world, providing access to some of the most trusted and proven medicines to those who need them most.

Are you an experienced electrical engineer with profound knowledge of industrial electrical power generation and distribution? Do you want to act as a global lead in international construction projects with a consulting mindset to internal customers? Then we are looking for you!

DPS Group Global is currently looking for a Global Lead Utilities Engineer.

DPS Group Global is currently looking for a Global Lead Utility Engineering with in-depth knowledge of sustainable (food / beverage) utilities.

DPS Group Global is momenteel op zoek naar een Electrical Engineer in de Den Bosch regio.

Process Engineer required for a Pharmaceutical organisation based in the Leinster area. Primary focus is to support ongoing manufacturing processes and new product introductions.

DPS Group Global is currently looking for a Design Automation Engineer in the Nijmegen area.

DPS currently have a requirement for an EDMS Manager with a Biotech Client based in North Dublin

Process Cleaning Representative An opportunity now exists for a Process Cleaning Representative to support the small molecule side of the business of our client. The successful resource ideally needs to have a third level degree qualification, good interpersonal skills and an interest in problem-solving.

Maintenance Engineer required for a Pharmaceuticals organisation based in South Leinster.

Quality Specialist The successful Quality Specialist will be responsible for ensuring that all products managed by External Quality Assurance (EQA) are manufactured, packaged, analyzed, released, stored, and distributed in accordance with expectations and all applicable regulatory requirements.

Both Upstream & Downstream Technical Specialists required in support of a new drug substance technology transfer at a Dublin based BioPharmaceutical facility.

DPS Engineering are recruiting for a GMP Documentation Specialist on behalf of a Dublin based Pharmaceutical Company

Technical Writer / Documentation Specialist This position is for a Technical Writer in the Production/Quality area of the formulation and API facilities. Reporting to the Shop Floor Data Integrity Lead. 

DPS is currently looking for a Document Controller, who plays a key role in the delivery of DPS’s multi-disciplinary projects. The Document Controller is responsible for ensuring all documentation and drawings are up to date and at the correct revision, also support project personnel with all aspects of Document Control.

DPS have a requirement for a Project Scheduler to work Client Side on a large scale Pharmaceutical project in South Leinster. 

DPS Engineering is looking for a Document Control Lead to assist with a BioPharma client of ours in the Providence, RI area. This individual would be expected to setup a document management system suitable for the multi-million dollar project and would be a key person responsible for managing the document flow for the project from A/E, CM, Vendors, C&Q, etc.

DPS is looking for a Senior Quality Assurance Specialist to work with a BioPharma client in the MA and NH areas. Ideal candidates should have a strong understanding of GMPs and have previous experience working within highly regulated pharmaceutical/biotech facilities. The QA Specialist will support the delivery of quality system activities at the Manufacturing Facility to ensure commercial and/or clinical products are manufactured and distributed in accordance with all regulatory and corporate requirements.

DPS is seeking an established and knowledgeable Quality Specialist to work with a BioPharma client in the Boston, MA area. Successful candidates should have previous experience working with other departments to ensure the quality of products and compliance to internal procedures and external standards. Must have previous experience with TrackWise, change controls, and deviations.

DPS is seeking an established and knowledgeable Quality Assurance resource to work with a pharmaceutical client in the Boston, MA area. Successful candidates should have previous experience providing QA support of internal and external audits of sites for testing and manufacturing activities at all stages of product life cycle. Providing support for other QA activities will also be included in the role. This position requires travel 25% of the time domestically and internationally.

DPS is seeking a talented and energetic Talent Acquisition Specialist who will serve as the primary point of contact as it pertains to management of staff augmentation services. He/she will be responsible for full lifecycle recruitment from candidate engagement to placement by developing and maintaining the relationship with the Client and Candidates through best in class augmentations services.

Voor een onsite rol is DPS Group Belgium op zoek naar een Support in Microbiological Lab Analyses.

Scheduler (DPS Group East Cork area) The successful Project Planner / Scheduler will provide lead support on various projects as part of a DPS Group project team to deliver projects for our clients on schedule. Our clients are primarily in the Pharmaceutical, Chemical and Micro Electronic industry sectors. DPS provides full EPCMV (Engineering, Procurement, Construction Management and Validation) services to its clients.

DPS Engineering is looking for a capable Deviation Investigator to work with a BioPharma client in the Boston, MA area. Ideal candidates should have a strong understanding of GMPs and have previous experience working within highly regulated pharmaceutical/biotech facilities. This individual will provide direct support to Manufacturing while investigating process deviations; designing effective CAPA; developing and delivering successful training; and monitoring and measuring ongoing performance of Bulk Manufacturing quality systems.

DPS is looking for a QA Systems Manager to work with a pharmaceutical client in the Cambridge/Lexington, MA area. Ideal candidates should have a strong understanding of GMP and have previous experience working within highly regulated pharmaceutical/biotech facilities. This individual will be expected to support day-to-day quality operations via oversight of all elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), investigations, excursions, Out of Specifications (OOS), change control, batch review and disposition, and data integrity in support of biologics manufacturing production. Additional responsibilities include supporting/conducting internal audits and external supplier/vendor audits. This role may also require 20 – 40% travel.

DPS is looking for a proven Senior Project Engineer to work with a BioPharma client in the Boston, MA area. Ideal candidates should have a strong understanding of GMPs and experience providing Project Engineering support in highly regulated or pharmaceutical/biotech facilities.

DPS is looking for a Senior Utilities/Facilities/Plant Engineer to work with a BioPharma client in the Southern MA area. Ideal candidates should have strong experience with clean and plant utility systems including but not limited to WFI, Clean Steam, HVAC, and other related systems. This individual must also have strong previous biologics and capital projects experience.

DPS is looking for a Quality Investigations Manager to work with a pharmaceutical client in the Cambridge/Lexington, MA area. Ideal candidates should have a strong understanding of GMP and have previous experience working within highly regulated pharmaceutical/biotech facilities. This individual will support day-to-day quality operations via oversight of elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), investigations, environmental and utility excursions, Out of Specifications (OOS), and change controls in support of biologics manufacturing production. Additional responsibilities include supporting internal and/or third party or regulatory agency audits.

DPS is seeking a highly motivated individual with a BioPharma client in the Boston, MA area. As a Process Engineer, you will provide process development and engineering support for technology transfers, process validations and GMP. Additionally, you will draft and review protocols, production procedures, and process development reports, and provide technical assessment and approval for engineering and process changes as well as documentation pertaining to process development, qualification, and validation to meet regulatory requirements. This role will focus on aspects of ensuring a robust, scalable and efficient manufacturing processes to produce late-phase human clinical trial and commercial gene transfer vector products.

DPS is seeking a knowledgeable Process Validation Engineer to work with a BioPharma client in the Boston, MA area. Preferred candidates should have experience working within aseptic and GMP environments.

DPS is looking for a Senior Quality resource to work with a pharmaceutical client in the Cambridge/Lexington, MA area. Ideal candidates should have a strong understanding of GMP and have previous experience working within highly regulated pharmaceutical/biotech facilities. This individual will support day-to-day quality operations via oversight of all elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), investigations, excursions, Out of Specifications (OOS), change control, batch review and disposition, data integrity, and training in support of biologics manufacturing production.

DPS is looking for a Senior Quality resource to work with a pharmaceutical client in the Cambridge/Lexington, MA area. Ideal candidates should have a strong understanding of GMP and have previous experience working within highly regulated pharmaceutical/biotech facilities. This individual will support day-to-day quality operations via oversight of all elements of the Quality Management System (QMS), including but not limited to deviations, Corrective and Preventive Actions (CAPAs), investigations, excursions, Out of Specifications (OOS), change control, batch review and disposition, data integrity, and training in support of biologics manufacturing production.

DPS is looking for an experienced Process Development Engineer to work with a pharmaceutical client in the Boston, MA area. This individual would need to be able to step in with minimal training to execute based on the project goals and must be able to work independently with minimal supervision. The ideal candidate will be able to accomplish multiple tasks concurrently and think independently.

DPS is seeking a knowledgeable Metrology/Calibration professional to work with a pharmaceutical client in the Lexington, MA area. The ideal candidate should have previous pharmaceutical or biotech knowledge and will support an existing manufacturing facility through troubleshooting and maintenance.

QA Rep Engineering The successful QA Rep Engineering will have a BSc (Hons) Micro, Engineering, Biochemistry, Chemistry, Analytical or a related discipline with ideally a minimum of 2 years similar QA experience.

DPS Engineering currently have an opportunity for a Maintenance Planner with a Midlands based Pharmaceutical client.

DPS currently have an opportunity for a CQV Engineer with a Midlands based Pharmaceutical client.

Maintenance Reliability Engineer (East Cork area) The successful Maintenance Engineer will report to the Maintenance Business Unit Manager and will be. You will be responsible for the development and implementation of a mechanical integrity program