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Validation Engineer Job Title: Validation Engineer – Process Equipment Validation Engineer to support C&Q activities. * Assist in the management of process equipment validation aspects of the project to ensure that both GMP compliance and project milestones are achieved. * Review of vendor validation lifecycle documentation
Additional Keywords: Validation Engineer, Instrument Engineer, Medical Device Engineer, Pharmaceutical Device Engineer, Validation Instrument Engineer, Medical Instrumentation Engineer, SIP Engineer, Steam in Place Engineer.
Working with the LotusWorks team as a Validation Engineer you will be responsible for the technical leadership and development of the validation project team. You will also be responsible for the assignment of validation activities to the validation project team.
Excellent opportunity for a Validation Engineer join one of the top 10 global companies in the medical device outsourcing industry. * Generate validation documentation (URS, IQ, OQ, PQ and process characterisation studies & validation reports) and assist in the execution of protocols for equipment, process, utilities, methods and computerised systems.
As CSV Engineer you will report directly into the Site Validation Manager and be responsible for implementation of the Site Validation Policy as well as compliance with regulations and current industry standards. Exciting Permanent CSV Engineer role with Leading Biopharmaceutical comapny to be based on site in their GMP facility in West Dublin.
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CAI is looking for individuals with at least 2 years of experience in the areas of commissioning, validation, automation and quality/compliance to join our team in Europe. Commissioning Agents, Inc. is always looking for individuals in the areas of commissioning, validation, automation and quality/compliance to join our team in Europe!
As a validation engineer, you will primarily be responsible for developing, maintaining and improving a standardised validation process for the Plant to ensure compliance to required regulations within the engineering function.
Headcount Engineering is seeking a Validation Engineer for our biopharmaceutical client in Limerick for an initial contract period of 12 months. * Experience in Validation specifically continuing (re-validation or maintaining a qualified state in relation to equipment/utilities).
Develop Validation Documentation to support new process/product introductions and existing business continuity and process improvement requirements. * Work with the various departments / groups in development and execution of validation activities associated with new equipment / product or IM System upgrades.
Validation Engineer required for a Mayo / Sligo based Pharmaceutical client. Validation Engineer * Requirement to hire a contract Validation Engineer to work on multiple projects across the site as well as ongoing site compliance activities. * The candidate should be an experienced Validation Engineer.
Job Title: Validation Engineer Our Client is looking for an experienced, enthusiastic and capable engineer to join validation engineering team in high volume medical device manufacturer to support a wide range of projects.
Experienced in equipment development and validation This is a contract position. Roles & Responsibilities * Preparation Equipment Binder documentation * User Requirements Specifications * Risk Assessments * Identify a modular testing strategy based on the vendors Equipment Specification (ES) and defined in a test plan (EDST) * Requirements Traceability Matrix (URS, ES & EDST)
Our client is an innovative start-up in Limerick and seeking a Validation Engineer with experience in software to join their team in a role which is brand-new and reports to the CTO. • Responsible for the creation of validation documentation including validation plan, validation report, traceability matrix for custom and COTS software
Excellent position now open for a Validation engineer in Limerick on a 12 month contract with possible extension. * Having knowledge of and ability to provide Interpretation and Guidance on Regulations, Corporate, Divisional and Site Local procedures as they relate to validation activities.
Strong working knowledge in the application of quality engineering tools and techniques with key emphasis on GAMP5 and Master Validation Planning. * Generate applicable documentation to Automated Equipment Validation of Quality * Write the necessary validation protocols, & amendments of the Quality Management * Development of validation projects.
Validation Team Lead role within the Project Technology Group role. Responsibility for coordinating activities of the validation team. Validation Scheduling * Evaluation of validation requirements in relation to new equipment, change controls and new * Allocate Validation resources to projects and validation activities as required to meet project
Our client, a major medical manufacturer , have an opening for a Quality Validation Engineer with specialization in process design and technical writing, validation, technical support at their site in Dublin. Quality Validation Engineer Process Design, Process Validation, Verifications & Technical Writing
Working with the LotusWorks team as a Software Validation Engineer you will ensure that best software validation practices are employed by all departments. * Ensures that software validation is carried out in compliance with site/corporate policies and SOPs.
A leading biopharmaceutical client of Headcount Engineering is seeking Cleaning Validation Engineers for its Limerick facility. * Experience in Validation, specifically cleaning validation * An excellent understanding of how Manufacturing/Cleaning Validation/Cleaning Equipment works * Ability to maintain and update Cleaning Validation Plan.
The Computer Systems Validation Engineer is responsible for implementation of the Site Validation Policy as well as compliance with regulations and current industry standards. We are seeking a Computer Systems Validation Engineer.
Senior QA Validation Specialist is required for an innovative and rapidly growing Biopharmaceutical company in Limerick. o Experience in Continuing Validation (re-validation or maintaining a qualified state in relation to equipment/Utilities).
Our client, a leading regulated manufacturing company are looking for a Quality Validation Engineer to join their team. * Strong working knowledge in the application of quality engineering tools and techniques with key emphasis on GAMP5 and Master Validation Planning.
A CLEANING VALIDATION ENGINEER is required by CareerWise Recruitment for our Limerick based biopharmaceutical client. This is a fantastic opportunity for an Engineer/Specialist with 3+ years Cleaning Validation experience to join a leading biotech company in Limerick.
As Senior Validation Engineer you will lead and manage projects for the validation of equipment, processes and products to meet all safety, quality, regulatory and operational requirements.
As a software validation engineer, you will be a member of the validation team in the Quality department. Excellent position now open in Galway for a Software Validation Engineer (salary ca. You are primarily responsible for documentation and execution of validation activities in accordance with validation plans and procedures.