Senior Validation Professional- Medical Device
6 hours ago
Senior Validation Professional-Medical Device About the Company My client is a leading multinational medical device company, specialising in innovative solutions that improve quality of life. About the Position This is an exciting opportunity to manage the validation lifecycle and Advanced Product Quality Planning (APQP) processes for this busy medical device manufacturing plant. Key Responsibilities Lead and Manage the Validation Team: Oversee daily operations, allocate work, and ensure high performance and quality output. Drive Validation Projects: Serve as the lead on all validation projects, ensuring alignment with protocols and production requirements. Ensure Compliance: Develop strategies to meet regulatory requirements, maintain validation policies and procedures, and manage the Validation Master Plan. Lifecycle Management: Oversee product and process transfers, manage PFMEA and control plans, and support post-validation activities. Technical Execution: Lead IQ, OQ, PQ, and process development activities, including DOE and MSA, to ensure process effectiveness. Cross-Functional Collaboration: Work closely with Operations, Planning, and Engineering teams to validate manufacturing processes. Regulatory Audits: Participate in regulatory audits and ensure all validation activities meet industry standards. Experience/Requirements Minimum 5 years of high-volume engineering experience in the medical device industry 3 + years of experience in validation processes BA/BS Engineering or related technical qualification Proficient in statistical techniques, including Minitab, Six Sigma (preferably Green Belt), and Sampling Plans/Sizes. Strong experience in process development, DOE, and risk management (FMEA). Excellent documentation skills and a strong understanding of process validation. Proven ability to lead a team, manage projects, and communicate effectively across departments Strong problem-solving skills and the ability to work independently or as part of a team. Remuneration Package A competitive package is on offer which will include salary, benefits and bonus. Contact For more information on this position or other life sciences roles, please contactCharlie Biggeron oremailor simply click the apply button. To view all live jobs with Brightwater and market insights, please visit our website: Skills: medical device validation equipment process development Leadership
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Senior Product Engineer
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Dublin, Ireland PM Group Full timeOverview Who we are PM Group is an employee owned, international project delivery firm with a team of 3,700 + people. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organisations. We are focused on growing a sustainable business centred...
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(Apply in 3 Minutes) R&D Project Manager
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Dublin, Ireland Allstarmedicalsupply Full timeSTEM Recruitment Partners are collaborating with a leading medical device R&D company to offer a 12-month contract for an R&D Project Manager. This role offers competitive contractor hourly rates. Role Overview: Reporting to the Senior Director of Device Engineering, the Project Manager will lead technical projects, including planning, scheduling, budget...
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▷ High Salary! Validation Engineer New
5 hours ago
Dublin, Ireland CPL Full timeOn behalf of our client, a global medical devices company, we are currently recruiting for a Validation Engineer. This is a permanent, full-site position site based in North Wicklow/South Dublin. Reports to Maintenance, Engineering and Validation Manager Essential responsibilities - Compilation and execution of validation protocols - Compilation of...
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Dublin, Ireland Stem Recruitment Partners Full timeSTEM Recruitment Partners are working with a medical device org, based in Dublin, that is seeking an experienced Senior Design Verification Engineer to join their R&D operations. This role focuses on verifying medical device projects to ensure comprehensive validation throughout development, readiness for formal testing, and effective lab management of...
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Senior QA Validation Specialist
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Dublin, Ireland PE Global Full timeDescription: PE Global is currently recruiting for a Senior QA Validation Specialist on behalf of a leading biotech company based in Dublin South. This is an initial 18-month contract role. Overview: We are seeking an experienced Senior Quality Assurance Professional to provide quality direction and oversight for activities related to the installation of new...
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Senior QA Specialist
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Dublin, Ireland Life Science Consultants (LSC) Full timeLSC have a great contract opportunity for a Senior Quality Assurance Specialist (Validation) to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 7 years of experience working in the pharmaceutical or biotechnology industry and are ready for...
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Medical Sales Representative
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(Urgent) Senior Software Verification Engineer
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Quality Technical Services Manager
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Dublin, Ireland Brightwater Full timeQuality Technical Services Manager -1 Year FTC About the Company My client is a leading multinational medical device company, specialising in innovative solutions that improve quality of life. About the Position My client isseeking a dynamic and detail-oriented professional to ensure the smooth operation of our manufacturing processes, prevent disruptions,...
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