Average salary: €32,025 /yearly
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€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- ...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,...SuggestedFull timeContract workWorldwideFlexible hours
- ...training system as required. Act as subject matter expert for the training system. Work with relevant departments to prepare the Annual GMP and EHS training plans for the site. Facilitate classroom and skills training as required ( limited requirement). Understand the...SuggestedVisa sponsorshipRelocationHybrid workFlexible hoursShift work
Merck Gruppe - MSD Sharp & Dohme
Dunboyne, Co. Meath19 hours ago - ...cross functionally, focusing on meeting and tracking to schedules and embracing an interdependent work culture. Experience working in a GMP / regulated environment is desirable. Organisation Skills – Ability to manage multiple priorities and know when to escalate issues...SuggestedFull timeContract workWorldwideShift workWeekend work
- ...Laboratory Systems processes related to sample management, testing, and validation. Ensure Laboratory Systems compliance with evolving GMP requirements. Provide training on Laboratory System procedures. Participate proactively in process improvements, change controls,...SuggestedContract workWorldwide
PSC Biotech
Dunboyne, Co. Meath19 hours ago - ...schedule and quality of project-related documentation/electronic records for equipment, utilities assigned. Responsible for ensuring GMP equipment and Clean Utilities are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations....SuggestedContract workFor contractors
- ...in industry Direct experience of device development and manufacturing operations activities for device or drug/device systems in a GMP environment Experience in the implementation of device design controls and ISO/FDA requirements as applicable to device design Demonstrated...Suggested
- ...system release. Provide QA review and approval of Change Controls, Deviations/CAPAs, SOPS and related documentation for compliance to GMP and site requirements at the facility. Provide QA oversight to the qualification/validation, technical transfers, regulatory...SuggestedFull timeContract workWorldwideFlexible hours
- ...withexperience level of candidate. Strong technical writing capability and previousexperience authoring reports and investigations in a GMP environment Competent in analysing complex situations and showpractical problem-solving capabilities. Ability to work...SuggestedContract workWorldwide
PSC Biotech Corporation
Dunboyne, Co. Meath4 days ago - ...: Level 7 qualification in a science or engineering discipline desired. A level 6 with a minimum of 3+ years’ experience in a GMP Manufacturing requirement shall be deemed equivalent Competent in troubleshooting and show practical problem-solving capabilities....SuggestedFull timeContract workWorldwideShift work
- ...by continually reviewing best practice in relation to both commercial and quality issues and ensuring 100% ethical work standards and GMP compliance. - To revise SOPs as required by the Lead Analyst or client representative. - To review analytical data for GMP compliance...SuggestedFull timePart timeFlexible hours
- ...and 10+ years of demonstrated experience within Quality compliance within large molecule manufacturing industry Expert knowledge of GMP requirements for multiple regulatory agencies Expert knowledge of large molecule manufacturing processes (for biologics and/or vaccines...SuggestedFull timeContract workFor contractorsLong term contractVisa sponsorshipWork at officeLocal areaRemote workRelocationHybrid workFlexible hoursShift work3 days weekMonday to Thursday
- ...client Health Authority inspections, internal audits, and supplier audits. Contribute to continuous improvement initiatives to enhance GMP compliance. Collaborate with cross-functional teams to provide quality-related consultation. Stay current with pharmaceutical...Suggested
NRL
Dunboyne, Co. Meath2 days ago - ...procurement, construction, start-up, and validation. Review and approve Change Controls, Deviations, CAPAs, SOPs, and related documents for GMP compliance. Oversee qualification/validation, technical transfers, regulatory approvals, and operations. Review validation...SuggestedContract workWorldwide
PSC Biotech
Dunboyne, Co. Meath4 days ago - ...best practices for Laboratory Systems processes supporting sample management, testing, and validation. Ensure compliance with evolving GMP requirements and trends. Train personnel on Laboratory System procedures. Participate proactively in process improvements,...SuggestedContract workWorldwide
PSC Biotech Corporation
Dunboyne, Co. Meath19 hours ago €46.83k - €79.64k per annum
...functionally, focusing on meeting and tracking to schedules and embracing an interdependent work culture. • Experience working in a GMP / regulated environment is desirable. • Organisation Skills – Ability to manage multiple priorities and know when to escalate issues...Contract workTemporary workFixed term contractWorldwideShift workWeekend work- ...pharmaceutical manufacturing facilities in a maintenance or engineering team is an advantage. Experience of project execution/management within GMP manufacturing is an advantage. Experience with maintenance management and reliability programs is an advantage. Experience of...Contract work
