\nDesign Stage:
\n● Leads design of Pharma pure fluid utility requirements, ensuring:
\n○ Design meets pharma norms, regulations
\n○ In line with customer User Requirement Specification
\n○ Participate in the evolution of the products and range of products
\n○ Compliance with local health & safety regulations
\n
\nProject Stage:
\n● Effectively project-manage and streamline the flow of work of all assigned projects
\nuntil handed over.
\n● Attend the necessary “hand-over” meetings to identify and understand the ‘conditions
\nof contract’ and ensure that the purchase order reflects the scope of the work.
\n● Conduct design reviews to verify that the sales design complies with the project
\nrequirements, procurement budgets and installation method statements before it is
\nadopted.
\n● Check through the water analysis, the mechanical/hydraulic and electrical
\nengineering design requirements of the proposed system.
\n● Monitor progress, prepare progress reports and attend progress meetings as
\nrequired.
\n● Ensure that all potential variations are identified, quantified and agreed with the
\nclients’ agents in accordance with the Project Programme.
\n● Obtain appropriate assistance and input from other people/departments in a timely
\nmanner so as to meet the requirements of the Project Programme.
\n● Prepare a “hand-over” pack for the Service Department and schedule system
\ncommissioning.
\n● Carry post-project meetings as necessary with a view to improving performance.
\nFinance:
\n● Monitor the project for scope, time and budget.
\n● All variations to be approved by the client before work commences.
\n● Prepare cost spreadsheets to determine the project value and margin.
\n● Monitor, maintain and improve the project margin where possible without
\ncompromising technical quality or standards.
\nCustomer Liaison:
\n● Represent the Company on all matters relating to the project and control all related
\ncorrespondence and documentation.
\n● Carry out all client communications politely, professionally and courteously,
\npromoting good relations and efficiency and delivering a professional approach at all
\ntimes.
\n● Plan all site operations with the relevant organisations briefed on the technical, safety
\nand timescale requirements of the project.
\n● Attend site meetings with the Client, Engineering Consultant and Subcontractor when
\nrequired and issue the relevant follow-up minutes.
\n● Ensure that standard and special systems Operating Handbooks are issued to the
\nclient in accordance with the project timeframe and, where appropriate in larger
\nsystems, ensure that clients receive thorough operating training.
AutoCAD
\n● Produce accurate and legible Process Flow Schematic; P&ID and Plant Room
\nLayout.
\n● Drawings to ensure that the equipment fits into the space provided with ample
\nservice access in accordance with Company Procedures and Work Instructions.
\n● Manage the generation of all documentation in accordance with Company
\nProcedures and Work Instructions and the required Project Programme.
\nValidation
\n● Produce validation documentation which comprehensively tests the system supplied;
\ni.e. Installation Qualification Protocols, Commissioning Sheets, and Operation
\nQualification Protocols, in accordance with the required Project Programme.
\n● Ensure that all validation documentation is correctly completed by the Company and
\nthe client and ensure that a copy is filed in-house.
\n● Ensure that the ‘all water treatment system’ documentation and certification supplied
\nby our suppliers and contractors is traceable to the equipment supplied.
\n● Collate the ‘all water treatment system’ certification documentation into a presentable
\ncertification file and prepare the necessary quantity of copies for the client in
\naccordance with the required Project Programme.
\n● Collate the ‘all water treatment system’ O&M documentation into a presentable
\nOperator’s Manual and prepare the necessary quantity of copies for the client in
\naccordance with the required Project Programme.
\n● Upon receipt of the Handover Certificate from the client, ensure that a copy of both
\nthe Operator’s Manual and the Certification are available in-house.
Requirements:
\nEducation:
\n● Degree in Mechanical or Chemical Engineering.
\nSkills and experience:
\n● Good understanding of pharma norms, regulations, GMP, GAMP, ASME BPE.
\n● Familiarity with Pharma pure fluid utilities including:
\n○ Softening
\n○ Reverse osmosis
\n○ Electrodeionisation
\n○ Purification
\n○ Multiple effect distillation
\n○ Pure steam generation
\n○ Storage and distribution of pure fluid utilities
\n○ Validation of pharma systems
\n● General understanding of waste water technologies.
\n● Ability to solve problems and meet project deadlines.
\n● Ability to create P & I D drawings and write Functional design Specifications.
\n● Be cost-conscious and be able to critically analyse new and existing designs to
\ngenerate cost reductions.
\n● Have experience of managing multiple projects and are familiar with using project
\nplans.
\n● Have strong analytical, problem solving and decision making skills.
\n● Have excellent communication skills with the ability to communicate effectively with
\ntechnical and non-technical disciplines.
\n● An awareness of the potential risks to health and safety on all clients' properties.
Full-Time
No salary listed
Junior, Mid
Dublin, Ireland
The role is based in the office in Celbridge, Co. Kildare, and involves regular travel to Europe, particularly Denmark and Switzerland.
Company Size
10,001+
Company Stage
IPO
Headquarters
Aubervilliers, France
Founded
1853
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Paid Vacation
Paid Sick Leave
Phone/Internet Stipend
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