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- ...Position: CSV Engineer. Location: Dublin, Ireland. PACIV, a global leader in industrial automation solutions with offices in Ireland... ...hybrid role (3 days per week on site). Applicants must have a valid EU Work Permit and Irish Residency Job Description The Control...SuggestedFull timeContract workHybrid workNo agency3 days week
- ...environmental impact and foster vibrant and diverse communities around the globe. SUMMARY CSV & Data Integrity Specialist will ensure that all GxP relevant computerised systems are validated in accordance with applicable regulatory requirements (e.g. EU GMP Annex 11 FDA 21 CFR...SuggestedFull timeLocal areaWorldwide
- ...culture. We are committed to equal employment opportunities that foster an inclusive environment. Posiition Summary The CSV Validation Engineer serves as the subject matter expert (SME) within the Validation team leading validation strategies for major capital projects...SuggestedFull timeLocal area
- ...for our deliverables are being met. Overview: Reporting to the Digital Project Manager and CSV Lead, specifically responsible for Computer System Validation. The CSV engineer will be responsible for the development of key quality documents, such as Quality...SuggestedContract workWorldwide
- ...Reporting to the Project Manager and CSV Lead specifically responsible for Computer System Validation. The CSV engineer will be responsible for the development of key quality documents such as Quality Assurance (QAPs) test plans Requirements Traceability Matrices...SuggestedFull time
- ...Overview We are seeking a motivated Junior CSV Engineer with a strong interest in automation systems used in pharmaceutical manufacturing. This role supports the validation of automated platforms equipment control systems and associated software to ensure compliance...SuggestedFull time
- ...benefits career progression educational support and much more. Lab IT CSV Engineer 1607 SimoTech has a new opportunity for an engineer with 3 years experience in Computer Systems Validation and Laboratory IT systems to join our team. The successful candidate will...SuggestedFull timeHybrid work3 days week
- ...experience in the planning, document generation, support or execution of CSV activities in a biologic drug substance manufacturing plant. A... ...to have qualification in Project Management and Computer Validation. Very Strong Collaboration, Compliance and Communication Skills...SuggestedPermanent employmentContract workTemporary workWorldwide
- ...Job Title: Computer System Validation (CSV) Engineer Location: On-site (Limerick) Role Overview: The CSV Engineer will be responsible for ensuring that all computerised systems within the pharmaceutical environment are validated in compliance with industry...Suggested
Project Delivery Partners
Limericka month ago - ...our expanding team. We are looking to add an experienced Junior CSV Engineer to the team of our pharmaceutical client based in Dublin... ...minimum of 4 years ~1-3 years experience with Computer systems validation ~5+ years experience working in a GMP environment ~ BS in a...SuggestedFull time
- ...At Hays Specialist Recruitment we have a great opportunity for a CSV Engineer to join our Biopharmaceutical client in Dublin on an initial 12-month contract. The CSV Engineer (Computer System Validation Engineer) is responsible for validating and maintaining computerised...SuggestedContract work
- ...Role: CSV Engineer Location: Dublin Contract: 12-month contract Daily rate contract. At Hays Specialist Recruitment we have... ...initial 12-month contract. The CSV Engineer (Computer System Validation Engineer) is responsible for validating and maintaining computerised...SuggestedDaily paidContract work
- ...looking for dedicated, innovative and driven talent to join our expanding team. About the role: We are currently looking to hire an CSV Validation Engineer to join our projects team in Cork, supporting multiple projects with the worlds leading Pharmaceutical and Biotech...SuggestedPermanent employment3 days weekCork8 days ago
- ...at AbbVie. We are now looking for a Site Process and Cleaning Validation Lead to join our diverse Technical Centre leadership team at... ...Expertise in the relevant subject matter areas –example cleaning, CSV, Aseptics, process, CPV ~ Understanding of Process Validation,...SuggestedPermanent employment
- ...Designation/Service provider QA Validation Specialist Reporting to whom Senior Manager QA Ops Summary : QA Validation... ...and regulatory advice for qualification activities including CSV qualification and data integrity. Provide QA Validation...SuggestedFull time
- ...QA Validation Specialist Equipment Utilities 6 mth contract Summary : QA Validation role to ensure Qualification of Equipment / Computerised... ...on qualification validation and computerized system validation (CSV) activities including data integrity compliance. Lead...Full timeContract work
- ...QA Validation Specialist Lab 6 mth contract Summary : QA Validation role to ensure Qualification of LIMS and Laboratory instruments is... ...Serve as QA Validation SME overseeing Computer System Validation (CSV) activities including URS FS RA IQ OQ PQ and validation reports....Full timeContract work
- ...role with full Stryker benefits. Member of the Global GQO-QA Validation team as Staff Validation Engineer. Support validation projects... ...support for those specialties (e.g. Computer System Validation (CSV) / Qualification of Buildings Facilities and Utilities (BFU) / Measuring...Full timeContract workHybrid workLocal area
- ...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...Contract workTemporary workWork at officeWorldwide
- ...Hanley Calibration are currently looking to hire Senior Validation Technicians for a Blue Chip pharmaceutical site in Limerick. Requirements Strong Commissioning Experience. Good understanding of the IQ, OQ, PQ and Design Process GMP Experience in Pharmaceutical background...Permanent employmentFor contractorsApprenticeship
- ...automated systems including PLC, SCADA, DCS, Historian and process equipment. Support specification, procurement, implementation, and validation of automated systems, ensuring adherence to GMP procedures on-site for all related tasks Manage and execute automation change...Full timeFor subcontractorLocal area
- ...committed to equal employment opportunities that foster an inclusive environment. POSITION SUMMARY: Write review and execute Validation Plans Protocols and Reports for Albumin Projects ensuring compliance to all relevant global and local quality and validation...Full timeContract workLocal area
- ...budget and ensuring timelines for our deliverables are being met. A fantastic opportunity has arisen for a Quality Assurance Validation Specialist . You will support new Validation and Commissioning programs across site as well as the periodic review of validated systems...Full timeContract workWorldwide
- ...V alidation Engineer – Permanent or SubContractor Opportunity We are seeking a talented Validation Engineer to join our team, where you’ll have the opportunity to support cutting-edge projects and make a real impact on product quality and compliance for our client based...Permanent employmentFor subcontractorFlexible hours
- ...CLEANING VALIDATION SPECIALIST Job Purpose: Pfizer Grange Castle seeks a Cleaning Validation Specialist to work within the Cleaning Validation Team supporting new product introduction and cleaning validation activities across the site. A critical enabler to product manufacture...Full timeHybrid workRelocation packageWorking Monday to Friday
- ...Are you looking for a 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...Contract workTemporary work
- ...We have fantastic opportunity for a Validation Engineer to join our Quality team in Dungarvan Co Waterford. The purpose of this of this role is to execute the Metrology schedule and Metrology helpdesk activity required to support the Operations function operating at the...Full timeFor contractorsRemote work
- ...outside of the function and organisation. ~ Excellent communication skills with the ability to formulate thoughts in a clear and concise manner to provide clarity and a path forward on any issues. ~ Applicants must have a valid EU Work Permit and Irish Residency...Full time
- ...Validation Engineer - County Longford. In this role you will be responsible for supporting all validation activities associated with the successful qualification of new tools / product introduction. You will support the organisation to achieve new product introduction objectives...Full time
- ...Quality / Validation Engineer - County Westmeath. In this role you will provide Quality Assurance support to ensure the Quality System is of the highest standard with a particular focus on validations and non-conformances. Key Responsibilities: - Implement and maintain...Full time
