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- ...Position: Computer System Validation (CSV) Engineer. Location: Munster, Ireland. PACIV, a global leader in industrial automation solutions with offices in Ireland, the United States and Puerto Rico, and serving the Life Science, F&B and Utilities industries, is looking...SuggestedFull timeNo agency
- ...Senior CSV Engineer We are seeking an experienced Senior CSV Engineer to support a major pharmaceutical manufacturing and capital... .... The successful candidate will take a lead role in the validation and compliance of computerised systems, ensuring systems are implemented...SuggestedFull time
£48 per hour
...Job Purpose Lead and support the validation and life-cycle maintenance of site computer systems and analytical equipment in line with regulatory... .... Experience leading or significantly contributing to CSV / data integrity programmes at site or network level. Prior experience...SuggestedLong term contractContract work- ...wide range of elements in order to improve product quality and promote a more responsible use of resources. Summary: The Validation Specialist is responsible for creating and maintaining validation documents, such as internal validation protocols, Installation Qualification...SuggestedFull timeWorldwideFlexible hours
- Excellent opportunity for a Validation Engineer with a Leading Life Sciences company in Sligo. The Validation Engineer will support site expansion and revalidation projects , requiring 3–5 years’ validation experience across autoclaves, lyophilisers, parts washers...SuggestedTemporary work
- Excellent opportunity for a Validation Engineer with a Biopharma in Sligo on a 6 month contract . The Validation Engineer will support on validation related to Autoclaves, lyophilsation, parts washers. The ideal candidate will have validation execution experience, Aseptic...SuggestedContract workTemporary work
- ...Are you a Validation Engineer looking to work on cutting-edge pharmaceutical and biotech projects in Ireland? CAI is seeking a QA Validation Engineer to support qualification and validation activities for laboratory and process equipment across leading pharmaceutical and...SuggestedFull time
€54.2k - €88.4k per annum
...science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Senior QA Validation Specialist to join our Quality Assurance team. This position offers the opportunity to contribute to a fast-growing, science...SuggestedFull timeFor contractorsWorldwide- ...potentially even some of our international clients around the globe. Role accountabilities: As a Commissioning, Qualification and Validation (CQV) Engineer, you will join a team delivering projects across the pharmaceutical sector, including Biotech, API, Sterile...Suggested
- ...company established in 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...SuggestedFull timeFor contractorsWorldwide
- ...Validation Engineer – Senior ________________________________________ CAI Overview: Are You Ready? CAI is a professional services company established in 1996 that has grown year over year to nearly 700 people worldwide. For Life Sciences and Mission Critical industries...SuggestedFull timeTemporary workWorldwide
- Role: QA Validation & Technical Operations Specialist (Sterile Drug Product) Location: Dublin Contract: 12-month contract 50% Remote... ...qualification. You will support GMP design reviews, and CQV / CSV / Automation through all phases of the project up to and including...SuggestedContract workRemote work
€60k - €100k per annum
...product and service lines and regulated domains (e.g., GCP, HIPAA, CSV). This role will work closely with cross-functional global teams... ...activities and deliverables, such as process definition, validation testing, and product releases/changes for in scope products and systems...SuggestedRemote jobWork at officeLocal areaWork from home- ...project teams. Identify and manage implementation risks, recommending appropriate mitigation actions. Support Software System Validation (CSV) activities in line with FDA guidelines and GMP requirements. Update requirements, design, and security documentation as...SuggestedFull timeImmediate start
- ...Manufacturing Execution Systems) with automation layers to enhance data flow, traceability, and paperless manufacturing Computer System Validation (CSV) & GxP Compliance Author and execute validation documentation (URS, FS, DS, IQ, OQ, PQ, Validation Strategy) in accordance...SuggestedContract workFixed term contractWorldwideShift work
- ...edit data files, ensuring quality and consistency. Conduct data validation and error-checking routines. Upload, transfer, and confirm... ...management systems. Familiarity with common file formats (PDF, CSV, XML) and basic troubleshooting. Awareness of GDPR and best practices...Long term contractFull timeHybrid workWork at officeWorldwide2 days week
- ...CQV activities · Manage stakeholders to the DeltaV commissioning and qualification process · Partner with Computer System Validation (CSV) and Digital Data Quality (DDQ) teams to ensure compliance with applicable standards and policies. · Partner with internal...Full time
- ...alidation) delivers automation, controls, instrumentation, and validation solutions to manufacturing and regulated industries. For over 30... ...and commissioning reports. Support Computer System Validation (CSV) activities, including URS, risk assessments, IQ/OQ/PQ protocols,...Full timeContract work
- ...Ethernet, Foundation Fieldbus). Collaborate with Automation, CSV, QA, and Operations teams during project execution. Ensure compliance... ...21 CFR Part 11 requirements. Maintain documentation, SOPs, validation records, and infrastructure reports . Requirements...
Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL)
Dunboyne, Co. Meathmore than 2 months ago - ...Support root cause analysis, deviations, and CAPA execution Perform basic system administration and maintenance activities Support CSV activities including protocol execution, testing evidence, and documentation support Collaborate with Operations, Process...
Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL)
Dundalk, Co. Loutha month ago - ...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 hours1 day week
- ...(word or excel) Ensure engineering calculations and drawings meet required robust industry and legal standards Responsible for validation of Intermediate & Graduate Engineer input into designs Support the delivery of projects in accordance with the expectations of the...For contractorsHybrid workWork at office
- ...on call duties, in line with business needs Requirements: ~ Fully qualified Electrician with 2+ years management experience ~ Valid Verification & Certification qualification (QC number) ~ Valid Safe Pass an advantage ~3+ years domestic experience ~ Excellent...Weekend work
- ...Responsibilities: Assist with the end-to-end payroll process, ensuring accuracy and timely completion of all pay cycles Process and validate timesheets (both manual and digital), resolving any discrepancies Support onboarding of new employees, maintaining accurate...Permanent employment
- ...applying industry best practices and benchmarking data to create robust and achievable schedules. Progress Monitoring: Track and validate work progress, updating schedules in line with actual performance. Variance Analysis: Identify and report on schedule variances, including...Permanent employmentFull timeHybrid workRemote workFlexible hours
- ...Bring deep, hands-on understanding of the sportsbook engine: odds and price ingestion, market and event modelling, bet placement and validation, liability and risk/trading management, cash-out, and the settlement pipeline. ~ Scale and latency. Architect for the throughput...Odd jobLong term contractRemote work
- ..., Biotechnology, Pharmaceutical Sciences, or related discipline ~10+ years’ experience in Commissioning & Qualification / CQV / Validation ~ Strong working knowledge of GMP requirements, FDA and EMA regulations ~ Strong hands-on upstream and downstream bioprocess knowledge...40 hours per weekFull timeContract workWorldwide
- ...additional tasks as reasonably required by the Check Supervisor. Requirements Knowledge, Skills and Experience: • Must hold a valid, unrestricted EASA B1 Licence. • Boeing 737NG Type rating endorsed on license (Essential). Additional Boeing 737 Max Type Rating...Flexible hoursShift work
- ...Excellent problem-solving skills and attention to detail. Ability to work both independently and collaboratively in a team setting. Strong communication skills and a customer-focused approach. Valid driver's license and any required automotive certifications....
- ...and blueprints. Strong leadership and team management capabilities. Knowledge of safety regulations and best practices in pipefitting. Effective communication and problem-solving skills. Valid driver’s license and relevant pipefitting certifications....
