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The Validation Engineer has a key role in ensuring the on-going validation and compliance of equipment, systems and processes at Sanofi Ireland. Excellent opportunity for a Validation Engineer to join our team in Waterford! The position being advertised is an exciting and challenging Validation Engineer role in the Sanofi Waterford site.
My Client a major Pharmaceutical company are recruiting for a Lead Validation Engineer. Applications are invited for a Validation Engineer – this may be considered as a secondment opportunity. Reporting directly to the Validation Manager. While the role will be focused on Process Validation, the candidate should be an SME in other areas of Validation.
Responsible for overall product & system validation & verification of products manufactured. Support the business requirements and implement the organization's Validation programs in line with company objectives, ensuring compliance with International & Regulatory Standards.
A Validation Engineer is required by CareerWise Recruitment for a leading company based in Donegal. * Co-ordinate all validation activity within the company working directly with the Engineering & Operations Departments.
The successful candidate will have a strong background in equipment validation and a good understanding equipment installation & technical transfers. Generate & execute validation protocols as required - Resolve and assist in the closure of deviations initiated during qualification / validation execution.
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The purpose of this Job is to develop and conduct appropriate procedures regarding the Qualification and Validation of coating equipment, processes, and systems. Design for Manufacture, ensuring conformance with current equipment, process, and systems validation regulations - Responsible for validation activities for NPI's / product transfers
A leading employer in Galway requires a team player to step into their established validation team. Ideally you will have at least 2 years in a Quality role with some experience of carrying out or supporting validation projects.
The Validation Engineer will be part of the QA Team reporting to the CAPA & Validation Manager. Manage and co-ordinate the Validation Change Control System, Validation Master Plan and associated schedule and all related documentation .
I am delighted to be assisting this lovely SME manufacturer in Shannon find a Validation Engineer to join their team. It is an exciting opportunity for an experienced validation engineer to join their our growing business. 3-5 years' experience in a validation role in either Medical Device or Pharmaceutical Industry.
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.
CAI is looking for individuals with at least 4 to 6 years of experience in Cleaning validation and quality/compliance to join our team in Europe. CAI is looking for individuals with at least 4/6 years of experience in the areas of Cleaning Validation and quality/compliance to join our team in Ireland.
Equipment Validation Engineer - Medical Devices - Galway • Contract position for a Validation Engineer. This position will provide design and verification control for equipment projects within the R&D department The role will provide direct contributions to the creation of lifecycle documentation for biomedical equipment.
Urgently require a Validation Engineer for a 12 month contract with proven and demonstrated experience on clean utilities or compounding systems including CIP/SIP for immediate start.]]>
The successful validation engineer will join the validation team to add expert knowledge and assist the validation manager to deliver with company targets. A leading medical device manufacturer is urgently seeking an experienced Validation Engineer to join their manufacturing facility based in South Dublin.
Our client, a leading medical devices innovator now requires a validation engineer for a 6 month contract • Contract position for a Validation Engineer. This position will provide design and verification control for equipment projects within the R&D department.
Opportunity in Mayo for an Equipment Validation Engineer to join leading manufacturing company. Process Validation against Corporate SOP/FDA/EMEA requirements. Accountable for writing, executing & reporting validation documentation (DQ / FAT / IQ / OQ / PQ / PPQ / pFMEA). Performing of validation functional testing as required. Assist in execution of validation protocols.
Permanent job for Validation Engineer to join leading manufacturing multinational in Galway. Responsible for writing, executing & reporting of all validation activities including but not limited to (DQ / FAT / IQ / OQ / PQ / PPQ / pFMEA). Development of project plans for Validation/Qualification projects.
Plans, coordinates, and participates in a compliant validation process for production automation/enterprise systems which requires formal validation documentation under appropriate regulatory requirements and company manufacturing standards. * Lead process improvement projects to improve the validation of computerized systems
I am delighted to be assisting this lovely SME manufacturer in Shannon find a Junior Validation Engineer to join their team. It is an exciting opportunity for an experienced validation engineer to join their our growing business. 3-5 years' experience in a validation role in either Medical Device or Pharmaceutical Industry.
Our client, a progressive and innovative pharmaceutical company in Waterford, has an opportunity for a Process Validation Engineer to join their team. The primary function of the role is to ensure process validation activities are completed in line with internal and regulatory procedures and guidelines.
The Computer System Validation Engineer will provide IT systems validation and compliance expertise for newly purchased instruments and support of existing instruments. We are seeking an enthusiastic and experienced computer system validation engineer to join the CSV team on a long-term contract basis.
Mentoring of Quality Validation Engineers & training non Validation individuals in the requirements of Validation. Experienced Validation Engineer. Experienced Validation Engineer reqired for Bray Plant. 3 to 5 years’ experience in a Quality Engineering or Validation role. Fully competent in Regulatory requirements of Validation
The newly hired QE’s will provide Quality Engineering and Process Validation services for medical devices and become involved with many projects including supporting the qualification of new equipment and up-grades to existing equipment.
Experienced Quality and Validation Engineer. Excellent opportunities within the Nypro Bray Plant for experienced Quality Validation Engineers. Develops validation and qualification protocols and tracks execution of protocols in support of project timelines. Develops & executes validations through all phases i.e. FAT, IQ, SAT, OQ & PQ