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
- ...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
- ...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
- ...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
- ...years industry QC experience. ~ MPS (Manufacturing Process Stream) experience is a must. ~ Knowledge of domestic and international GMP regulations, cGMP’s, policies, performance and budget management. ~ Excellent trouble shooting and problem-solving skills. ~ Ability...SuggestedContract workVisa sponsorshipWork at officeRelocationHybrid workFlexible hoursShift work
- ...technical leadership. Ability to think logically and be proactive under pressure. Knowledge of regulatory and quality guidelines (GMP). Strong focus on quality, safety and compliance. Excellent analytical and technical skills. Preferably broad knowledge of...SuggestedVisa sponsorshipWork at officeRelocationHybrid workFlexible hoursShift work
- ...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
- ...Skills and Education required: ~ Level 6 qualification in a science or engineering discipline desired. ~2+ years experience in a GMP Manufacturing requirement shall be deemed equivalent ~ Ability to work independently and within a cross-functional team. ~...SuggestedFull timeContract workWorldwideShift workWeekend work
€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...SuggestedContract workTemporary workFixed term contractWorldwideShift workWeekend work- ...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
- ...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