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- ...continuous improvement objectives. The role requires an individual with expert level technical skills with HMI and PLC systems, gained in a GMP (Medical Devices, Pharma, Life Sciences or Biotech) environment. Essential Duties and Responsibilitiesinclude, but are not limited to,...SuggestedPermanent employmentFull timeFor contractorsRemote workRelocation
- ...statistical control of processes to allow cost saving. Mentoring and training team and cross functional groups as required (induction, GMP etc) Contributing to the development, maintenance and improvements of the policies and procedures to align to best practices,...SuggestedTemporary workRemote workFlexible hours
- ...progressively responsible positions Competent working knowledge of recognized Quality Management Systems (e.g. ISO9001/ ISO13485/ ISO14971/ GMP), Awareness of relevant laws and regulations (e.g. CE/ FDA/ PAL) Broad knowledge of engineering and technical applications applied...SuggestedPermanent employmentContract work
- ...high quality regulatory submission dossiers. Supports regulatory compliance activities, including manufacturing site registration & GMP audits as needed. Acts as company representative, developing and maintaining positive relationships with the device owners through oral...Suggested
- ...external audits. Communicate concerns regarding environmental impact, health, or safety issues to management. Maintain compliance with GMP, GLP, and GDP to ensure quality in all work aspects. Perform additional duties as directed by the supervisor. Identify and...Suggested
- ...maximise overall equipment effectiveness and efficiency. Ensure that all Engineering work and designs are carried out to appropriate GMP, QA/Regulatory Authority standards and Environmental Health and Safety standards. Support the development of new processes in...Suggested
- ...Materials & Compliance Oversight – Establish inspection plans, frequencies, and test methods for incoming materials and ensure GMP compliance . Quality System Leadership – Drive continuous improvement initiatives in compliance with ISO and FDA regulations ....SuggestedFull time
- ...continuous improvement objectives. The role requires an individual with expert level technical skills with HMI and PLC systems, gained in a GMP (Medical Devices, Pharma, Life Sciences or Biotech) environment. Essential Duties and Responsibilitiesinclude, but are not limited to,...SuggestedPermanent employmentFull timeFor contractorsRemote workRelocation
- ...environment. Proven track record supporting internal operations teams and/or external manufacturing partners. Strong knowledge of QMS, GMP, FDA and ISO13485 requirements. Experience with root cause analysis, process improvement methodologies and non-conformance...SuggestedContract workFlexible hours
- ...delivery of medical devices that change lives. Responsibilities: Ensure compliance to all applicable regulatory standards and current GMP procedures and practices. Perform product defect analysis. Routine final functional testing, product release criteria testing/...Suggested
- ...Engineer I Duration: 12 Months Location: Galway, Hybrid Role Responsibilities: Support routine Sterility Assurance activities e.g GMP, Standards Compliance, Cleanroom Risk Assessment, Limits review, Dose Audit activity, Cycle Requalification, Supplier Change control...SuggestedHybrid work
€80k - €100k per annum
...monitor KPIs , dashboards, and performance metrics. Ensure full compliance with relevant regulatory frameworks, including ISO 13485 , GMP , and FDA 21 CFR Part 820 . Champion continuous improvement initiatives across operational areas. Contribute to strategic...SuggestedPermanent employmentContract workFor contractorsLong term contract- ...use of FMEA’s, asset criticality survey’s, and craft/operator engagement. This Job function will change where update procedures to GMP, EHS, Technical / New Equipment, Quality Procedures & BOP’s are made. Major Responsibilities Manage overall engineering spend of...SuggestedFull timeImmediate startShift 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
- ...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
- ...motivate and develop through understanding, personal development and lifelong learning. Ensures department adherence to regulatory and GMP requirements. Drives Operation Growth initiatives within the production area, delivers high quality functional deliverables....No agency
- ...RESPONSIBILITIES To coordinate and oversee daily packaging operations, ensuring that production targets are met in accordance with GMP, safety, and quality standards. Supervise the day-to-day running of assigned packaging lines by leading and coordinating all line activities...Contract workImmediate start
- ...ethic. • Demonstrated process and continuous improvement mindset. • Excellent time management, organisational, communication and interpersonal skills. • Ability to work independently or as part of a team. • Strong commitment to quality, safety and GMP standards....Full timeShift workMonday to Thursday
- ...manufacturing technologies. Requirements: - Mechanical or biomedical engineering degree or equivalent. - Proven experience within a GMP regulated Medical Device Industry. - Project Management experience or alternatively a key core team member as part of a project team....Contract workHybrid work
- ...performance. Assist R&D and Quality in the qualification of all production equipment and facilities including review and approval of GMP qualification protocol (veterinary manufacturing), reports and risk assessments. Develop, manage and monitor departments budgets/...Permanent employmentFull time