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- A global traceability systems provider in Ireland is seeking a Validation Specialist responsible for creating and maintaining validation documents. This role involves developing templates, conducting risk analysis, and ensuring compliance with industry standards. The ideal candidate...Suggested
- A global healthcare company is seeking a Technical Lead for Validation in Dublin. This role involves leading validation projects, ensuring compliance with regulatory standards, and collaborating with various departments on validation efforts. Ideal candidates will have a degree...Suggested
- A global healthcare leader is seeking an experienced Validation Specialist for their Cootehill site in Ireland. This role is crucial for coordinating validation activities and ensuring regulatory compliance within a dynamic team. Ideal candidates will have at least 4 years of...Suggested
- ...QA Validation Specialist Dublin 22, Grange Castle Cpl in partnership with our client Pfizer are Seeking a QA Validation Specialist to join the team at their state-of-the-art Dublin, Grange Castle Plant for an 11-month fixed term contract with Hybrid working model....SuggestedFixed term contractHybrid work
- A pharmaceutical company in Dublin is seeking a QA Systems & Validation Specialist responsible for ensuring all GMP-related changes and validation activities comply with regulatory requirements. The ideal candidate will have at least 3 years of experience in the pharmaceutical...Suggested
- ...text_color="" animation_type="" animation_direction="left" animation_speed="0.3" animation_offset=""] QA Resources are looking for a number of contract QA Validation Specialists for an exciting project based in Cork. Role and requirements: Review of IQ/OQ/PQ protocols...SuggestedContract work
- ...The role PE Global is currently recruiting for a QA Validation Specialist on behalf of a leading pharmaceutical company based in Dundalk. This is an initial 11 month contract role. Overview A fantastic opportunity has arisen for a Quality Assurance, Validation Specialist...SuggestedContract work
- ...Position Summary The QA Systems & Validation Specialist is responsible for ensuring that all GMP-related changes, systems, and validation activities comply with regulatory requirements and site Quality standards . This role provides subject matter expertise across...Suggested
- QA Resources is seeking multiple contract QA Validation Specialists for a project in Cork. The role involves reviewing and developing validation protocols, ensuring compliance with regulatory standards, and supporting equipment qualification. Candidates must possess a Bachelor...SuggestedContract work
- A leading pharmaceutical company in Dundalk is hiring a QA Validation Specialist for an 11-month contract. The role involves ensuring compliance with cGMP and cGLP standards, collaborating with various teams for QA support, and approving Validation Lifecycle documents. Candidates...SuggestedContract work
- ...Job Spec for QA Validation Contract Contract for 6-12 months. Role is mostly on site could be scope for small amount remote but most weeks would be fully on site especially during execution and review of protocols. Summary : QA Validation role to ensure...SuggestedContract workRemote work
- ...We are now hiring a QA Validation Engineer on our Ballytivnan Medical Device site in Sligo. In this role you will join AbbVies Quality team supporting the development and maintenance of the site validation program and ensuring compliance with AbbVie FDA and cGMP standards...SuggestedFull time
- ...For more on 8 West Consulting visit our website on We are seeking an experienced QA/Test Engineer to join our QA Team. The role is based in Cork servicing the needs of our client. The role will report to the Software Project Manager. The successful candidate will work...SuggestedDaily paidContract work
- ...Safeguard quality and drive validation excellence as two new pharmaceutical products move toward commercial launch. R&D Partners is seeking a QA Validation Engineer to join a rapidly growing pharmaceutical company in Ireland. This is an exciting opportunity to contribute...SuggestedPermanent employment
- A leading multinational pharmaceutical company is seeking an experienced Senior QA Validation Specialist for their Dundalk facility. The successful candidate will oversee validation activities, ensure compliance with regulations, and manage the QA Validations team. Ideal candidates...Suggested
- ...we PSC Biotech is a leading Biotech Consultancy firm founded in 1996 headquartered in Pomona... ...has arisen for a Quality Assurance Validation Specialist . You will support new Validation... ...to. You will be the key in driving QA compliance to ensure standards are best in...Full timeContract workWorldwide
- ...Designation/Service provider QA Validation Specialist Reporting to whom Senior Manager QA Ops Summary : QA Validation role to ensure Qualification of Equipment / Computerised Systems / Facilities and Utilities is performed in compliance with...Full time
- ...QA Validation Specialist Lab 6 mth contract Summary : QA Validation role to ensure Qualification of LIMS and Laboratory instruments is performed in compliance with regulatory requirements company policy and procedures. Key Responsibilities: Support the introduction...Full timeContract work
- ...QA Validation Specialist Equipment Utilities 6 mth contract Summary : QA Validation role to ensure Qualification of Equipment / Computerised Systems / Facilities and Utilities is performed in compliance with regulatory requirements company policy and procedures. Support...Full timeContract work
- A global financial services leader in Ireland seeks a Test Automation Engineer specialized in Databricks and data platforms. This role involves developing automated testing frameworks and collaborating with data engineering teams to ensure data solutions' quality and reliability...Flexible hours
- An established industry player is seeking a Senior Staff Verification Engineer to join their innovative team. In this pivotal role, you will collaborate closely with design, firmware, and hardware teams to ensure the performance and correctness of cutting-edge power devices....Hybrid work
- ...new challenge in engineering? Step into a high-impact role where your expertise in utility validation helps power the future of pharmaceutical innovation. R&D Partners is seeking a QA Validation Engineer - Utilities to join a pharmaceutical company on a contract basis...Contract workTemporary work
- ...providing innovative healthcare and life science product and service solutions around the globe. Position Summary Manages Customer Validations ensuring that all validation activities are carried out in compliance with Customer requirements, STERIS policies & procedures, ISO...Local area
- ...the Position Provide Quality Assurance support to ensure the Quality System is of the highest standard with particular focus on validations and non-conformances. Key Responsibilities Write and execute validation protocols and reports for new product introductions,...Immediate start
- An established industry player in the semiconductor sector is seeking a skilled Analog Design Engineer to enhance their innovative IC design team. This role offers the chance to work on diverse projects in medical, automotive, and aerospace fields, providing a unique opportunity...
- ...Europe, Southeast Asia, the Middle East, Latin America, and Canada. Role Overview – Validation Specialist We are seeking an experienced Validation Specialist to join our established QA Team. Reporting to the Validation Manager, this role is central to coordinating...Contract workWorldwide
- ...Knowledge of manufacturing automation, machine design, development, and validation processes (GAMP 5 guidelines preferred). Experience in a... ...information on this role please contact Roisin Vaughan on consult@hero.ie or (***) ***-**** Check out all our open jobs on our HERO...
- A leading recruitment agency is seeking a Sterilisation Validation Engineer I for a hybrid role in Galway. This entry-level position requires a University degree and 1-2 years of experience in Sterility Assurance and GMP compliance. Key responsibilities include supporting sterility...Hybrid work
- ...Team Horizon is seeking a Sr Validation Engineer for various capital and equipment lifecycle projects joining a dynamic team. This role will be responsible for equipment validation in Sterile Fill Finish to ensure the maximum levels of performance and compliance are maintained...Hybrid work
- ...1996, that has grown year over year to nearly 700 people worldwide. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries. Are You...Long term contractFor contractorsLocal areaWorldwide
