Average salary: €17,288 /yearly
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- ...Job Description We are seeking a Data Reviewer to join our exciting Gene Therapy team in Dungarvan Co Waterford. 3+ years' GMP Pharma experience is required to apply for this role. The purpose of this job is the data review of scientific test procedures used...SuggestedFull timeContract workWorldwideFlexible hours
- ...Data Governance (DG) frameworks, policies, and procedures aligned with regulatory requirements and industry standards. As a Principal GMP Data Governance Specialist, a typical day might include the following: Evaluating current and emerging regulatory guidance and...SuggestedLocal area
€16 per hour
...We are currently looking for Full-time GMP Cleaners to join our team in a manufacturing environment in Dunboyne, Co Meath Working Pattern: Monday ~Sunday shifts , day 7AM-7PM and night 7PM -7AM Main Duties and Responsibilities Perform GMP cleaning per site specifications...SuggestedPermanent employmentFull timeImmediate startShift workNight shiftSunday- Consider joining Eurofins where people are the most important element in our business. Eurofins Biopharma Product Testing is a leading contract lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients...SuggestedFull timeContract workWorldwide
- The Associate Director, IT Operational Technology ensures the reliable operation of the IOPS IT/OT infrastructure and operations. The role will provide administrative direction and support for the daily IT operational activities for the Automation department. This may include...SuggestedTemporary workLocal area
- ...automation discipline, with a minimum of 5 years’ experience in industry, preferably in a pharmaceutical, biotechnology, blue chip or relevant GMP manufacturing environment. The ideal candidate will have excellent communication skills and strong problem skills. Candidates trained...SuggestedContract workFor contractorsRemote workRelocationHybrid work
- ...desirable. Excellent interpersonal communication skills, both written and oral. Excellent PC Skills Experience and good understanding of GMP (Good Manufacturing Practice). Works well within a team of designers/developers. Ability to work on own initiative; highly motivated.SuggestedPermanent employmentFull timeWork at office
- ...preventative maintenance schedules are adhered to •Achieve operational excellence targets •Minimise downtime Quality •Implement company GMP policies to maintain best in class standards •Facilitate inspections and action inspection reports •Identify and correct/continuous...SuggestedShift workWeekend work
- ...contractors’ roles for electrical/mechanical duties. # Ensure that electrical/mechanical activity in the production areas conforms to GMP standards and promotes a safe and healthy work environment through the continuous improvement of safety standards. # Flexible working...SuggestedFor contractorsFlexible hours
- ...Perform high-precision wiring tasks, ensuring components meet exact specifications. Conduct quality checks to ensure compliance with GMP and ISO standards. Prepare parts for anodising and assist in mechanical assembly during machine builds. Perform daily maintenance...SuggestedPermanent employmentContract work
€70k - €75k per annum
...electrical, and automation systems . Proven track record in project management , team leadership, and regulatory compliance (HACCP, GMP). Excellent problem-solving skills and a continuous improvement mindset . In return, you'll join a forward-thinking company...SuggestedPermanent employment- ...supervision and guidance of ISL technical and operational teams. Like all SGS personnel, they are committed to upholding stringent technical and GMP standards, ensuring the safety of medications for the multitude of patients relying on the products we test. Due to growth, we have...SuggestedFull timeLocal areaWorldwideFlexible hours
- ...contractors, during project conception and implementation stages. Experience of implementing and delivering large projects in complex GMP (Pharma, Life Sciences, Medical Devices) manufacturing environments is essential. Candidates without 2 or more years experience in this...SuggestedFor contractorsRelocationHybrid work2 days week3 days week
- ...production equipment Key Responsibilities Ensure that all work is completed in a manner aligned with the requirements of ISO 13485, GMP and the Technopath Quality Management System Performs other related duties as assigned. Assist in the manufacture of serum...SuggestedFull timeLong term contractLocal area
- ...Provide training to other technicians as required. Support safety and quality programs and initiatives. Ensure compliance with GMP standards in all practices. Perform other duties as assigned to support departmental and organizational goals. Skills and Requirements...SuggestedFull timeImmediate start
- ...General position summary: This role is responsible for providing support with real time inspection readiness activities supporting GMP quality. The role requires the ability to adapt to pipeline program milestones, whilst effectively ensuring alignment with corporate...Contract workTemporary workHybrid work
- ...maintaining laboratory management systems such as LIMS, LabX, Empower systems and an interest in coding/ script. ~ Experience working in a GMP Regulated Pharma/Biopharma company or related industry is desirable. ~ Have an understanding in analytical methodology (e.g., HPLC,...Full timeContract workWorldwideFlexible hours
- ...qualification in an Engineering discipline ~ Trade qualified will also be considered ~3-5 years experience in a regulated environment (GMP preferable) ~ Strong IT knowledge is required. ~ Strong trouble shooting and documentation skills ~ Working knowledge of ATEX...Full timeContract workFor contractorsShift workAfternoon shift
- ...Operating Procedures. Quality & Compliance ~Work closely with the Quality team to ensure adherence to Good Manufacturing Practices (GMP) during product development. ~Conduct and interpret chemical, physical, sensory, and microbiological tests, and take appropriate...Permanent employmentFull timeContract work
- ...implementation Manage traceability in the plant and coordinates required simulation for traceability. Conducts training in Food Safety, GMP in Production, GMP for Maintenance, PRPs etc Draft Manuals & Procedures and Manages Plant Quality Documentation System Coordinates...Permanent employment
€ 45 - 50 per hour
...SAP experience essential Supply Chain Mgr experience. This is an individual contributor role – no need for managing / leading team GMP experience Profiles such as Compliance Trade, Transport Logistics, etc. are not relevant to this role. This role is all about...Hourly payFull timeContract workWork at officeHybrid workFlexible hours2 days week1 day week€80 per hour
...Master’s degree in Engineering, Life Sciences, or a related field. 5–10+ years of experience in Commissioning & Qualification within a GMP-regulated environment, preferably in the pharmaceutical or biopharmaceutical sector. Proven leadership experience managing C&Q teams...Hourly payFull timeContract workFor contractorsWork at officeRemote workHybrid work€ 55 - 62 per hour
...project. Ensure the C&Q activities associated with the capital project are completed safely, as per schedule and in compliance with GMP and Quality Requirements. Commissioning & Qualification of Clean Utility Systems / Facility and Process equipment. Generation of...Hourly payFull timeContract workWork at office3 days week- ...Other duties as assigned Training will be provided Working Charge Hands Accountability Breaks Washdowns and Changeovers GMP Reporting of Small breakdowns and repeating issues Reporting of Quality Issues Waste Performance of Operators Key...Permanent employmentShift workNight shiftRotating shiftWeekend workSundaySaturdayMonday to Wednesday
- ...Wants to develop and help others. The ability to work under time pressure and with on own initiative. Safety, Documentation and GMP awareness / compliance. Safety/Quality focused. Experience of troubleshooting and repair of manufacturing equipment. Interest...Permanent employmentApprenticeshipShift workWeekend workSundaySaturdayMonday to Wednesday
- ...accordance with the requirements of the Product Specification File (PSF)/Marketing Authorisation (MA) and with Good Manufacturing Practice (GMP) for products manufactured * Ensure that products are manufactured in accordance with the relevant GMPs. * The Quality Assurance...Contract work
- ...Document Control systems and to work as part of the Quality Department to support Quality Systems. The person should have good knowledge of GMP specifically with regard to issue and version control of documents. As with all members of staff, this person is responsible for...Full timeContract workWorldwideFlexible hours
- ...activities of the Quality Assurance team, including handling product information requests ~Monitor compliance with food safety, legal and GMP (Good Manufacturing Practices) requirements ~Assist in the preparation of bi-annual REPAK packaging reports ~Perform daily product...Permanent employmentFull time
- ...site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup of GMP operations. The QC Systems and Compliance team provides support to the QC function owning cross lab programs such as electronic systems...Long term contract
- ...services tailored to the diverse needs of pharmaceutical facilities, biotechnology labs, medical device production centers, and more. From GMP and GLP laboratories to manufacturing pharmacies, clinics, and institutions, Exyte is a firmly established trusted industry partner...Local area