Average salary: €42,453 /yearly
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- Quality & Policy Expert Responsibilities to include but not be limited the following Partner... ...Operational Guidelines, and reinforce associated changes to operations teams. Make well... ...empathy 2+ years' experience in a quality control environment Written and verbal language...SuggestedPermanent employmentLocal area
- ...related changes, systems, and validation activities comply with regulatory requirements and site Quality standards . This role provides subject matter expertise across change control, validation, and quality systems , supporting manufacturing, laboratory, engineering, and...Suggested
- ...health for more at Job Function: Quality Job Sub Function: Quality... ...key quality systems/programs like Design Controls Technology Transfer Production & Process... ...communicating the quality management system GMP and associated documents and procedures to all staff...SuggestedFull timeLocal areaShift work
- ...and profoundly impact health for more at Job Function: Quality Job Sub Function: Quality Assurance Job Category:... ...Centered Design ISO 9001 Issue Escalation Problem Solving Quality Control (QC) Quality Management Systems (QMS) Quality Standards...Suggested
- ...line with an unwavering commitment to the quality and the delivery of safe and effective... ...established sampling and statistical process control procedures. Your expertise will help in... ...manufacturing records (paper / electronic) and associated manufacturing deviations are reviewed in...SuggestedFull timeRelocation packageFlexible hoursShift work
- ...the highest standards of professional excellence and quality assurance in the business with responsibility for... ...and approval of SOPs quality risk assessments change controls and otherdocumentation as applicable associated with QC functions. Review and approval of QC and...SuggestedFull timeContract workWorldwideOverseasFlexible hoursShift work
- ...Your mission at LINDAL The Quality and Compliance Systems Specialist is responsible for managing, maintaining and improving the Quality... ...regulatory requirements. This role ensures that documentation control, audits and systems are effectively administered, continuously improved...SuggestedLong term contractFull timeFlexible hours
€ 50 - 58 per hour
...leading aseptic manufacturing plant. The Quality Assurance Technical Support (QA TS)... ...areas (i.e. Inspection, Validation, Quality Control, Engineering, ), ensuring that programs,... ...validation Plans, Protocols, IQ, OQ, PQ and associated validation documents Review of...SuggestedHourly payFull timeContract workHybrid workWork at officeLocal areaRemote work1 day week- ...Laboratory Practices (GLPs). Demonstrates working knowledge of quality assurance systems methods and procedures. Demonstrates... .... Reviews manufacturing environmental monitoring and quality control data for in-process and finished products. Manage and execute...SuggestedFull timeFor contractorsLocal area
- ...countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections pharmaceuticals contract... ...the QA NPI Specialist will: Review and approve change controls corrective and preventive actions (CAPAs) deviations including investigation...SuggestedFull timeContract workWorldwide
- Wiodąca firma farmaceutyczna w Dublinie poszukuje Specjalisty Technicznego na umowę agencyjną na 12 miesięcy. Do zadań należy prowadzenie badań jakościowych oraz rozwijanie innowacyjnych rozwiązań dla wyzwań w produkcji. Wymagana jest dyplom z nauk ścisłych i doświadczenie w...SuggestedContract work
- A leading biopharmaceutical company is seeking a Specialist External Manufacturing in Dublin, Ireland. In this role, you will manage quality records for deviations and CAPAs, conduct site visits, and support supplier relations. The ideal candidate should have at least 3 years...SuggestedFlexible hours
- Quality Specialist - Hybrid Role We are currently seeking to recruit a Quality Specialist for a leading Pharmaceutical Manufacturer within... ...and review complaints and deviation investigations, change controls and CAPA’s. * Compiles data for reports and presentations - May...SuggestedContract workHybrid work
- ...Job Description Summary As a QA Specialist reporting to our Quality Leader youll manage the sites QA systems alongside other specialists... ...commitments (Regulatory Agency investigation audit etc.) change controls forms logbooks QC stability program validation and batch release...SuggestedFull timeRelocation packageWorldwide
- ...leading pharmaceutical company in Dublin is seeking a Technical Specialist for a 12-month agency contract. The role involves conducting quality investigations, supporting change management, and analyzing technical data to improve product quality. The ideal candidate will have...SuggestedContract work
- ...Contract Type: Regular Full-Time Area: Quality Would you like to join an... ...Support the manufacturing in‑process control (IPC) and end‑of‑batch reconciliation processes... ...of Grade A, B, C, D classified areas and associated controls in‑situ, utilizing RABS technology...Full timeContract workWorldwide
- ...As Quality Specialist (QA for QC) you will be responsible for supporting the Pharmaceutical Quality System (PQS) in place adhering to all... .... Participate and lead as necessary deviations CAPAs change controls suspect analytical result investigations laboratory and site investigations...Full timeContract workLocal areaWorldwide
- ...software & procedures are up to date and maintained within the Quality Department ensuring that all QC systems are kept up to-date maintained... ...policies and regulatory requirements. Ensure the necessary controls are in place to ensure excellence in regulatory safety and...Full timeFor contractorsFixed term contractLocal area
- A multinational healthcare organization in Dublin is seeking a QA Manufacturing (Shop Floor) Specialist. The role focuses on assurance of aseptic compliance and GxP standards within a new purification and aseptic filling plant. Ideal candidates will have a degree in Pharmaceutical...
- A leading biotechnology company in Dún Laoghaire is looking for a Specialist in Manufacturing to manage quality records and lead investigations. The role requires a deep understanding of Good Manufacturing Practices and experience in quality management systems. Ideal candidates...
- ...Compliance Specialist is responsible for documenting and establishing a quality system which ensures full compliance with all regulatory and... ...performance meetings. Coordinating change management change control and Change planning activities. Monitoring quality...Part timeFixed term contract
- ...protection efforts. This role involves working with senior management to implement programs and conduct inspections related to water quality and pollution investigations. The candidate should have a relevant degree and strong interpersonal skills. The position requires flexibility...Permanent employmentContract work
- ...a CSQ/CQV to become a key member of the Quality Team of a leading Pharmaceutical Multinational... ...and Validation (CQV) activities associated with the site supporting the transition... ...manufacturing processes, storage areas, controlled temperature units (CTUs) and shipping processes...Contract work
- An established industry player in the pharmaceutical sector is seeking a dedicated Quality Engineer to enhance their quality assurance processes. In this role, you will be responsible for ensuring compliance with regulatory standards and managing the quality system effectively...
€37.33k per annum
Multi Channel- Quality Expert Reviewer (Polish speaker) - Dublin City Centre Must be able to evidence previous Content Moderator Experience... ...Checking: Right to Work Criminal Record Check Any other associated checks Joining the team: Please note that this role is fully...Permanent employmentFull timeContract workCity centreWork at officeFlexible hoursShift work- ...Dundalk Ireland. This is a crucial role within the Quality organisation with responsibility for directly supporting... ...Perform QA review of SOPs risk assessments change controls and other documentation as applicable associated with Drug Substance manufacturing operations...Full timeContract workLocal areaWorldwide
- [fusion_builder_container type="flex" hundred_percent="no" hundred_percent_height="no" min_height="" hundred_percent_height_scroll="no" align_content="stretch" flex_align_items="flex-start" flex_justify_content="flex-start" flex_column_spacing="" hundred_percent_height_center...Contract work
- ...and ability including a high standard of suitability for the proper discharge of the office. Demonstrate experience in the area of quality & patient safety. Experience with Excel and data management to monitor metrics and KPIs. Proficient in Microsoft Word and...Part timeWork at office1 day week
- ...systems, cleaning, processes, storage areas, controlled temperature units (CTUs) and shipping.... ...of QA oversight to the CQV activities associated with the Dundalk Facility start-up... ...include but are not limited to: Ensure the quality oversight of the qualification/...
- ...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. You will support new Validation and Commissioning programs across site as well as the periodic...Contract work

