3 days ago Be among the first 25 applicantsThis range is provided by Gi Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.Base pay rangeDirect message the job poster from Gi GroupJob Title: Quality Systems ManagerLocation: Co.MayoSalary: €70-95k per annum DOERole: Onsite Full timeSummary:Our medical device client in Mayo is searching for an Experienced Quality Systems Manager with specialised experience in Documentation, Inspection, Training and Receiving for Quality systems. The ideal candidate will hold quality auditing experience within a medical device industry whilst leveraging expertise in the manging the processes and procedures for regulatory approval.Responsibilities:Adheres to all environmental, health and safety requirements, quality system procedures, and facility policiesLeader in compliance to all necessary regulationsAssesses conformance to documented procedures, regulatory, statutory, plant, divisional and corporate requirementsAssists in the establishment and maintenance of the assessment process including scheduling, performing and generating audit reportsResponsible for the management of the Internal Assessment Programme and the Documentation SystemCo-ordination of Audits by Regulatory Bodies and Contract Drug CompaniesResponsibility for the Supplier Quality Management programme which includes assessing and approving supplier quality systems, inspection of Suppliers for reduced inspection or certificationResponsibility for ensuring that an effective quality system is in place and provides assistance to management in the development of quality management systemsResponsibility for the management of the documentation, labelling and training departments. Responsible for the adherence to quality systems that involve the changes to procedures, labels and BOMs etc.Responsible for management of training in conjunction with area management for their respective areas.Responsible for the receiving and inspection and release of raw materials from 3rd party suppliers.Tracks the status of audit issues to help ensure that adequate actions are taken, documented and completed in a timely mannerMaintains adequate documentation to demonstrate that assessments have been performed as scheduledRequirements:Bachelor's degree or equivalent related experienceCertification from a Recognized Body (preferred)Three to five years of related experience required (preferably quality auditing experience within a medical device or other regulated industry)Excellent communication and writing skillsExcellent interpersonal skillsReasoning AbilityThe ability to exercise independent judgment and draw accurate conclusions based on available informationKSGalway__PRESENTJob Title: Quality Systems ManagerLocation: Co.MayoSalary: €70-95k per annum DOERole: Onsite Full timeSummary:Our medical device client in Mayo is searching for an Experienced Quality Systems Manager with specialised experience in Documentation, Inspection, Training and Receiving for Quality systems. The ideal candidate will hold quality auditing experience within a medical device industry whilst leveraging expertise in the manging the processes and procedures for regulatory approval.Responsibilities:Adheres to all environmental, health and safety requirements, quality system procedures, and facility policiesLeader in compliance to all necessary regulationsAssesses conformance to documented procedures, regulatory, statutory, plant, divisional and corporate requirementsAssists in the establishment and maintenance of the assessment process including scheduling, performing and generating audit reportsResponsible for the management of the Internal Assessment Programme and the Documentation SystemCo-ordination of Audits by Regulatory Bodies and Contract Drug CompaniesResponsibility for the Supplier Quality Management programme which includes assessing and approving supplier quality systems, inspection of Suppliers for reduced inspection or certificationResponsibility for ensuring that an effective quality system is in place and provides assistance to management in the development of quality management systemsResponsibility for the management of the documentation, labelling and training departments. Responsible for the adherence to quality systems that involve the changes to procedures, labels and BOMs etc.Responsible for management of training in conjunction with area management for their respective areas.Responsible for the receiving and inspection and release of raw materials from 3rd party suppliers.Tracks the status of audit issues to help ensure that adequate actions are taken, documented and completed in a timely mannerMaintains adequate documentation to demonstrate that assessments have been performed as scheduledRequirements:Bachelor's degree or equivalent related experienceCertification from a Recognized Body (preferred)Three to five years of related experience required (preferably quality auditing experience within a medical device or other regulated industry)Excellent communication and writing skillsExcellent interpersonal skillsGood presentation skillsReasoning AbilityThe ability to exercise independent judgment and draw accurate conclusions based on available informationKSGalway__PRESENTDesired Skills and ExperienceExperience requirements:* Certification from a Recognized Body (preferred)* Three to five years of related experience required (preferably quality auditing experience within a medical device or other regulated industry)* Excellent communication and writing skills* Excellent interpersonal skills* Good presentation skills* Reasoning Ability* The ability to exercise independent judgment and draw accurate conclusions based on available informationEducation requirements:* Bachelor's degree or equivalent related experienceShould you require any support or assistance, please contact your local Gi Group office.Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, pledge members for Neurodiversity in business, Disability committed members, Silver status pledge members for the Armed Forces Covenant, and Bronze trail blazers for Racial Equality matters.Gi Group Holdings Recruitment Limited group of companies includes Gi Recruitment Limited, Draefern Limited, Gi Group Recruitment Ltd, INTOO (UK) Limited, Marks Sattin (UK) Limited, TACK TMI UK Limited, Grafton Professional Staffing Limited, Encore Personnel Services, Gi Group Ireland Limited and Kelly Services (UK) Ltd. Gi Group Ireland Limited are acting as an Employment Agency in relation to this role.We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.Seniority levelSeniority levelMid-Senior levelEmployment typeEmployment typeFull-timeJob functionJob functionQuality AssuranceIndustriesMedical Equipment Manufacturing and Pharmaceutical ManufacturingReferrals increase your chances of interviewing at Gi Group by 2xGet notified about new Quality System Manager jobs in County Mayo, Ireland.Castlebar, County Mayo, Ireland 1 week agoQuality Systems, Documentation/Training & Receiving/Inspection ManagerCastlebar, County Mayo, Ireland 6 days agoWe’re unlocking community knowledge in a new way. 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