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- ...are looking for top talent to be part of the dynamic team and drive the growth of the business. Job Title: Computer System Validation (CSV) Engineer / Specialist Role Overview We are looking for a Mid-Level CSV Engineer to support validation activities for...SuggestedLocal area
- A leading manufacturing technology company in Cork is seeking a Mid-Level CSV Engineer to support validation activities for GMP-regulated computerized systems. The role involves executing CSV lifecycle deliverables, preparing documentation, and ensuring compliance with regulatory...Suggested
- A leading biotechnology firm is seeking a skilled Computer Systems Validation Engineer to join their Cork team. The ideal candidate will have over 2 years of experience in a similar role, particularly with DeltaV automation in pharmaceutical environments. Responsibilities include...Suggested
- ...much more. SimoTech has an opportunity for aComputer Systems Validation Engineerto join our team, supporting our client at a state-of-the... ...or Life Sciences . Minimum of 2 years’ experience as a CSV Engineer , supporting DeltaV automation in a pharmaceutical environment...SuggestedContract work
- ...Role Overview: The CSV Engineer will be responsible for ensuring that computerized systems used within the organization... ...role involves developing, writing, and executing Computer System Validation (CSV) protocols, managing documentation, and supporting audits...SuggestedFull time
- A leading medical technology firm is seeking a skilled Equipment/Validation Engineer to ensure compliance of automated production lines in Cork, Ireland. The ideal candidate will have a Bachelor's degree in Engineering and experience in validation within the medical device industry...Suggested
- A leading technology company is seeking a CPU Verification Engineer to validate micro-architecture concepts and work with Chip Architects in Cork. The ideal candidate will have significant experience in micro-processor verification and be able to develop test methodologies independently...SuggestedRelocation package
- ...Overview The role would be for a QC equipment validation Specialist role, specifically involving the full qualification of a bench top Near-Infrared (NIR) spectrometer. The managers specifically want someone at a senior level that can take full ownership of the project,...Suggested
- ...while championing patients every step of the way. Learn more at are searching for the best talent for a Senior Scientist Process Validation to be based in Cork Ireland. Our Global Focus in Advanced Therapies: Advanced therapy medicinal products (ATMPs) including...SuggestedFull timeLocal areaRemote workWorldwide
- ...Job Description Summary As the Global Head of Commissioning Qualification & Validation you will be responsible for developing leading and providing oversight to the commissioning qualification and validation (CQV) activities for Capital Projects and Continuous Lifecycle...SuggestedFull timeHybrid workRelocation package
- ...under budget and ensuring timelines for our deliverables are being met. Overview: This position reports to the Process Validation Manager and is responsible for multi-modality process validation activities in a cGMP environment. This position will coordinate and...SuggestedContract workWork at officeWorldwide
- 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 healthcare staffing agency is seeking an experienced NPI Engineer to provide technical leadership in process validation and new product introduction. This senior role involves driving validation strategy, mentoring junior engineers, and leading complex projects within...Suggested
- ...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 and reports for...SuggestedContract work
- ...Prioritize continuously in accordance with the understanding and validation of customer problems and needs. Stay updated with industry trends... ...design and system architecture concepts. Expert knowledge of CSV lifecycle with understanding of GxP (GLP/GCP/GMP) 21CFR Part 11...SuggestedFull timeTemporary workRelocation packageRemote work
- ...Software Engineer to join its IT Engineers (MES, MTS, Data Analytics, Validation & Infrastructure) on a customer site in Cork. The successful... .... Requirements: · Pharma experience and knowledge of GMP, CSV and data integrity requirements essential. · Degree qualification...Full time
- ...Responsibilities: Lead/Execute/Participate in Equipment and System Validation Lifecycle processes Qualification (IQ/OQ/PQ) Revalidation... .../vendors to complete validation tasks. Participate in CSV Validation Lifecycle processes Qualification (RS/QAP/UAT etc) CSV...Contract workFor contractorsWorldwide
- ...familiarity with the development and execution of C&Q documents as well as CSV deliverables such as Planning, User/Functional Requirements,... ...experience in the life sciences industries is preferred. Valid European Union work permits. Desired Soft Skills Excellent analytical...Permanent employmentNo agency
- A global technology innovator is seeking a Graphics Functional Design Verification Engineer in Cork. The role involves collaborating with GPU teams and creating verification methodologies for high-performance products. Ideal candidates will have over 5 years of experience in...Relocation package
- ...pharmacopoeial and regulatory requirements for laboratory equipment qualification and analytical testing. Understanding of Data Integrity & CSV, including 21 CFR Part 11 / Annex 11 compliance for computerised systems. What you'll get in return Flexible working options...Flexible hours
- ...with regulatory requirements. Collaborate with Quality Department to ensure projects and infrastructure meet site QA standards through CSV and other methodologies. Participate in high-risk remediation planning and execution to address OT security and reliability gaps....Local areaFlexible hours
- ...successful Project Manager will be responsible for managing the delivery of multiple projects within the digital space across MES Labs CSV Data Analytics and Infrastructure systems including a stateoftheart digital Material Tracking System. The ideal candidate will have...Full time
- ...Support root cause analysis, deviations, and CAPA execution Perform basic system administration and maintenance activitiesSupport CSV activities including protocol execution, testing evidence, and documentation support Collaborate with Operations, Process Engineering...
- ...be responsible for driving process efficiency and continuous improvement across all stages of complex assembly operations ensuring validated manufacturing systems consistently deliver exceptional product quality and operational excellence. Key Responsibilities Own...Permanent employmentFull timeContract workHybrid work
- ...trained in relevant analytical techniques. Train other analysts where appropriately qualified Carry out testing in accordance to the valid testing procedures and regulatory requirements Ensure that laboratory equipment is well maintained and calibrations are carried out...Full timeRemote workFlexible hours
- ...product process and quality system changes. Customer complaints: Approval of analysis reports and analysis of complaint trends. Validation: Define process and product validation requirements preparation and approval of Master Validation Plans protocols and reports...Worldwide
- ...tools and technical solutions Requirements: Strong communication skills in one of the listed languages EU citizenship or valid work/residency permit for Portugal Spain Greece or Bulgaria Whether you are drawn to the coast the city or a cultural adventure...Long term contractHybrid workRelocation packageRemote work
€40k - €58k per annum
...Staff Nurses for their Theatre Department, this is a permanent full time position. Required: * Must be registered with NMBI & have valid work permits * Must have 2 years plus Theatre experience ideally here in a hospital in Ireland or have strong Theatre experience...Permanent employmentFull time- ...integration development design reviews and collaborating with various departments including Business Operations Automation Technical Services Validation and Quality Assurance. The role will also support the deployment configuration and maintenance of the PAS-X MES system across...Full timeFor contractorsLocal areaShift work
- ...media domains Analyzing and evaluating search outcomes for App Store Content and conducting research using online tools to assess and validate query accuracy and intent by applying market expertise in conjunction with provided directives to evaluate the relevance and purpose...Extra incomeLong term contractPart timeRemote work

