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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
- ...Role Overview: The CSV Engineer will be responsible for ensuring that computerized systems used within the organization... ...This role involves developing writing and executing Computer System Validation (CSV) protocols managing documentation and supporting audits...SuggestedFull time
- ...deliverables are being met. Overview: Looking for senior Validation Engineer with team lead experience reporting to the Commissioning... ...to the various Validation disciplines e.g. FUE Qualification CSV New Product Introductions and Change Control. Develop...SuggestedFull timeContract workWorldwide
- ...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...SuggestedFull timeContract workWork at officeWorldwide
- ...Role: MSAT Validation Engineer Location: Cork / Hybrid 12-month Contract Hourly rate or PAYE The MSAT Engineer will be responsible for the following. Active engagement with the MSAT team, delivering a successful outcome for all MSAT validation activities using...SuggestedHourly payContract workFor contractorsHybrid work
- ...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
- ...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
- ...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...SuggestedFull timeContract workFor contractorsWorldwide
- ...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
- ...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 Engineering Quality...SuggestedFull time
- ...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....SuggestedLocal areaFlexible hours
- ...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...SuggestedFlexible hours
- ...Work Flexibility: Onsite What you will do: Designs validates and brings new products to market. Specifies precise new product functional requirements; designs tests and integrates components to produce final designs; and evaluates the designs overall effectiveness...SuggestedFull timeInternship
- ...product development team. KEY AREAS OF RESPONSIBILITY: What you will do: Technical Responsibilities: Conduct verification and validation testing of medical devices. This can include mechanical wear corrosion and other standardized or non-standardized testing. Under...SuggestedFull time
- ...volume budget movements, rebalancing, and reconciliations Owning month-end activities including accruals, reclassifications, and validation checks Supporting forecasting accuracy, cost tracking, and financial controls Maintaining audit-ready financial documentation...SuggestedLong term contractPermanent employmentContract workImmediate start
- ...Provides leadership in the development and management of Quality through the following actions: Supports GMP qualification and validation activities through execution of supplier/contractor audits and directing review of qualification/validation documents to provide oversight...Full timeFor contractorsFlexible hours
- ...please attach your CV via the link provided Please submit your updated CV in Word Format If you are living in Ireland and hold a valid work permit, we would love to hear from you, if however, you do not hold a valid work permit unfortunately we will not be in a...Long term contractPermanent employmentFull timeContract work
- ...to define project risk and to effectively manage project risks. Experience of statistical methods and design product and process validations would prove beneficial. Experience of Process mapping statistical methods and process/ product validations would prove...Full timeHybrid work
- ...commercial colleagues. Working closely with the wider GEA network you will help develop training materials advisory methodologies and validated propositions that enhance farm performance and customer satisfaction. This is a highly autonomous role offering freedom under...Full time
- ...controls with focus on regulatory and Marketing Authorization (MA) impact; escalate complex changes to QP. Evaluating qualification and validation documentation for manufacturing and packaging processes. Participate in supplier qualification activities and review critical...Permanent employmentFull timeFor contractorsTraineeshipLocal area
- ...implementation approaches Pull clean and merge data from internal systems to produce analysisready datasets Perform statistical validation of multivariate/chemometric models assessing robustness accuracy specificity and stability and prepare GxP-compliant validation...Full timeLocal area
- ...functional alignment, and maintain project momentum. Ensure project deliverables support manufacturing readiness, including process validation, documentation, training, equipment readiness, and quality system requirements. Champion continuous improvement by identifying...Full timeContract workTemporary work
€60k - €70k per annum
...please attach your CV via the link provided Please submit your updated CV in Word Format If you are living in Ireland and hold a valid work permit, we would love to hear from you, if however, you do not hold a valid work permit unfortunately we will not be in a...Permanent employmentFor subcontractor- ...Provide technical review and approval on QTS for the internal change management process. Responsible for API specifications process validation and AMTE activities Evaluate RSM strategies within the API portfolio and evaluating specification robustness Develop plans to...Full timeContract workHybrid workRelocation package
- ...rapid-response environment. Contracting & Supplier Management Coordinate contract reviews with Legal Finance and stakeholders. Validate pricing SLAs scope and contractual accuracy (training provided). Support supplier performance tracking and follow-up actions....Full timeContract workFlexible hours
- ...plant (Microbial Particulate Water). Perform or Review product testing (Bioburden and Endotoxin). Perform or Review product validations. Collect compile and analyse data and prepare laboratory reports. Assist in any investigations into out of specification results...Permanent employmentFull timeWork at officeWorldwideShift work
- ...and active travel schemes, Demonstratable experience of adhering to the Safety, Health and Welfare at Work (Construction) Regulations 2013 Willingness to travel and possession of a full, valid driver’s licence #LI-DB1 .. Why SYSTRA? Read more sur Why SYSTRA?Work at office
- ...goods as required. Operates shrink-wrap machine if assigned. Qualifications ~2 Years Experience in similar roles ~ Must have valid Counter Balance and Reach truck License ~ Special Requirements: Must have excellent work habits. Must be familiar with warehouse...Full timeLocal areaWorldwideShift work
€2,000 per month
...current work experience in Oncology in a JCI-accredited hospital in the Middle East (mandatory requirement) - With IELTS/OET certificate (valid until Oct 2026) - With an NMBI Decision Letter (preferable but not mandatory upon application; if you have one, it should be valid...Full timeRelocation package- ...~ Strong communicator; and comfortable in contributing to the overall hotel strategy. ~ Ability to develop and build relationships and influence with all levels of the business. ~ Must speak fluent English. Must be a resident of Ireland or have a valid work permit...Full time

