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- ...We are presently recruiting for a Production Manager for our clients, a large Engineering company in County Kerry. You will be responsible for overseeing the manufacturing process, ensuring that all production departments run efficiently and maintain high standards of product...SuggestedPermanent employmentFull time
- ...of the Manufacturing Team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors. As an... ...documentation Performing various tests and in-process sampling Reviewing, editing and revising completed batch records, logbooks, and...SuggestedLocal areaShift work
- ...the direction of all facets of commercial and/or clinical scale production of recombinant proteins in Raheen. As an Associate Director... ...implementing comprehensive manufacturing activities reports Reviewing, and/or approving Standard Operating Procedures, specifications...SuggestedLocal area
€217.24k - €261.05k per annum
...implementation of the Disciplinary Procedure e) To formally review the execution of the Clinical Directorate Service Plan with the... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with regulatory...SuggestedPermanent employmentFixed term contractTraineeshipFree visaRelocation packageWork at officeImmediate startRelocation- ...the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research... ...Social events Job Description We are seeking a Data Reviewer to join our exciting Gene Therapy team in Dungarvan Co Waterford...SuggestedFull timeContract workWorldwideFlexible hours
€217.24k - €261.05k per annum
...implementation of the Disciplinary Procedure e) To formally review the execution of the Clinical Directorate Service Plan with the... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with regulatory...SuggestedPermanent employmentFixed term contractFree visaRelocation packageWork at officeImmediate start€217.24k - €261.05k per annum
...implementation of the Disciplinary Procedure e) To formally review the execution of the Clinical Directorate Service Plan with the... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with regulatory...SuggestedPermanent employmentFixed term contractFree visaRelocation packageWork at officeImmediate start€217.24k - €261.05k per annum
...implementation of the Disciplinary Procedure e) To formally review the execution of the Clinical Directorate Service Plan with the... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with regulatory...SuggestedPermanent employmentFull timeContract workFixed term contractFree visaRelocation packageWork at officeLocal areaImmediate startRelocationFlexible hoursRotating shiftSundaySaturday€217.24k - €261.05k per annum
...effective from the commencement date of the appointment. It will be reviewed at 3 months & thereafter annually or at any time, but no less... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with...SuggestedPermanent employmentContract workFixed term contractTraineeshipFree visaRelocation packageWork at officeLocal areaImmediate startRelocationRotating shiftWeekend workDay shiftSaturday- ...catching digital LED display technology and audio systems. Our products bring excitement to professional, college and high school games.... ...Kanban replenishment. Attend daily materials meeting. Review error reports. Review quarterly and biannual physical stock counts...SuggestedFlexible hoursShift workSundayMonday to Thursday
- ...performance to identify areas for improvement and efficiency Reviewing consolidation opportunities at both SKU and supplier level Maintaining... ...planning and optimisation Actioning sales tenders and product requests from the Territory Managers and internal Sales team...SuggestedPermanent employmentFull timeWork at officeRemote workWork from home2 days week1 day week
- ...ensure the highest industry standards while delivering life-changing products worldwide. Job Summary We are hiring a QC Analyst to... ...laboratory setup and equipment qualification. Prepare and review laboratory procedures, protocols, and reports. Perform QC testing...SuggestedWorldwide
€217.24k - €261.05k per annum
...effective from the commencement date of the appointment. It will be reviewed at 3 months & thereafter annually or at any time, but no less... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with...SuggestedPermanent employmentContract workFixed term contractFree visaRelocation packageWork at officeImmediate startRelocationFlexible hoursNight shiftRotating shift€217.24k - €261.05k per annum
...effective from the commencement date of the appointment. It will be reviewed at 3 months & thereafter annually or at any time, but no less... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with...SuggestedPermanent employmentContract workFixed term contractFree visaRelocation packageWork at officeImmediate startRelocationRotating shiftWeekend work- ...who are one of the best at what they do. Duties: Complete auditing/ review of batch documentation to ensure compliance to SOPs, GMPs and applicable regulations Review and approve production and analytical documentation accompanying the release of drug substance, drug...SuggestedContract workWorldwideHybrid work
- ...facility. Responsible for assessing the microbiological quality of products, manufacturing equipment, manufacturing process areas, and... ...policies, and SOPs. Completing test records on time and peer reviewing data from other analysts for accuracy and completeness. Assisting...Local areaShift work
- ...one of the best at what they do. Duties: The QP will be involved in the review and certification of batches intended for use in clinical trials, to ensure compliance with EU GMP, the Product Specification File and the Clinical Trial Application. This role will encompass...Contract workHybrid work
- ...efficient administrative support, contributing to the sector's productivity and compliance. Key Responsibilities: QA Assistant Duties... ...stability samples. Equipment monitoring and stability unit trend reviews · Responsible for the Packaging /preparation of the Product...Flexible hours
- ...pivotal role in the design and development of our clients new modular product line. This position will be responsible for creating innovative... ...provide technical support during the manufacturing process. Review and approve design documentation, ensuring compliance with...Flexible hours
- ...innovation and leadership to carry out the following: • Be involved in the review and certification of batches intended for use in clinical trials, to ensure compliance with EU GMP, the Product Specification File and the Clinical Trial Application. • This role will encompass...Contract work
- ...Safety team at an upper-tier COMAH site. Duties: Participate in project design reviews, HAZIDS, Risk Assessments, and HAZOPS for proposed new equipment, modifications, and new product introductions. Ensure management of change processes are followed and serve as an...Contract work
- ...tomorrow Purpose Responsible for the efficient management of production personnel, resources, equipment and materials. Key... ...include Time and Attendance system, Holiday planning, Build Plan review Back Order review, Travel planning etc. ~ Works with EHS to identify...Worldwide
- Location: CorkRole: Permanent Details: Product Engineer required for a leading Electronics manufacturing company, reporting to the Engineering... ...(ESS, Environmental Stress Screen, generation) and design reviews. • Support of material issues in relation to sourcing and...Permanent employment
- ...We are currently seeking an experienced QC Data Reviewer to join our client’s Quality Control team. This role plays a crucial part in... ...management support, maintaining clear communication across Quality and Production teams. Maintain, update, and issue control prints, methods,...
€217.24k - €261.05k per annum
...implementation of the Disciplinary Procedure e) To formally review the execution of the Clinical Directorate Service Plan with the... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with regulatory...Permanent employmentFull timePart timeFixed term contractTraineeship40 hours per weekFree visaRelocation packageWork at officeImmediate startRelocationCity centreRotating shift€217.24k - €261.05k per annum
...effective from the commencement date of the appointment. It will be reviewed at 3 months & thereafter annually or at any time, but no less... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with...Permanent employmentFull timeContract workFixed term contractFree visaRelocation packageWork at officeLocal areaImmediate startRelocationShift workRotating shiftWeekend workAfternoon shiftWeekday work- ..., modifying existing assemblies as needed Conducting program reviews and documenting CNC operations Performing routine machine maintenance... ...the Engineering Manager Collaborating with engineering and production teams to ensure part quality and efficiency Supporting...Full time
€217.24k - €261.05k per annum
...effective from the commencement date of the appointment. It will be reviewed at 3 months & thereafter annually or at any time, but no less... ...in clinical audit and proactive risk management and facilitate production of all data/information required for same in accordance with...Permanent employmentContract workFixed term contractTraineeshipFree visaRelocation packageWork at officeImmediate startRelocationFlexible hoursNight shiftRotating shiftWeekend workDay shiftAfternoon shiftWeekday work- ...knowledge, innovation, and leadership to carry out responsibilities such as: The QP will review and certify batches intended for clinical trials, ensuring compliance with EUGMP, the Product Specification File, and the Clinical Trial Application. This role involves products...Contract workTemporary workWorldwide
- ...including method statements and preparation of clear comments. Review Contractor design submissions against Employers’ requirements... ...proficient in the use of computers in relation to document handling and production of reports. Full Clean Driving License. Have a...For contractorsLocal areaHybrid workFlexible hours