Medical Device Quality Engineer

Solventum is a company that enables better, smarter, safer healthcare to improve lives. We pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best.As a new company with a long legacy of creating breakthrough solutions...

Company ProfileSolventum is a cutting-edge health technology company that combines innovative thinking with operational excellence. We are dedicated to improving patient outcomes through our products and services.About the RoleThis position is responsible for maintaining and repairing complex medical devices, ensuring they operate efficiently and...

Teleflex is seeking a Medical Device QA Lead to join its Global QA Operations team. As a member of this team, you will play a critical role in ensuring the quality of medical devices throughout the distribution process.Your responsibilities will include:Supporting the Global QA L&D Operations processEnsuring adherence to regulatory and corporate compliance...

About the RoleWe are looking for a highly skilled Medical Device Technician to support production equipment in a medical device healthcare environment. The ideal candidate will have experience in repairing and troubleshooting automated electro/mechanical equipment failures.In this role, you will schedule and perform preventative maintenance procedures...

About UsTeleflex is a global leader in medical technologies, dedicated to improving healthcare outcomes through innovative products and services. Our purpose-driven approach enables us to create meaningful differences in patients' lives.Job SummaryWe seek a highly skilled Regulatory Affairs Associate to join our team in the EMEA region. The successful...

Solventum is committed to delivering innovative healthcare solutions that make a tangible difference in people's lives. As a Director of Medical Surgical International Plant Quality, you will play a pivotal role in ensuring the highest standards of quality excellence and compliance across our global operations.This challenging yet rewarding role requires a...

**About the Role:**The successful candidate will be responsible for leading software validation activities, overseeing validation plans, protocols, execution, and documentation. If you have experience working in regulated environments, specifically in medical devices, and possess strong knowledge of software validation principles and regulatory requirements,...

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear...

Thank you for your interest in working for our Company.Recruiting the right talent is crucial to our goals.On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum.We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding.Please bear with...

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear...

Engineering Recruiter - +353 86 440 3725 | choices@hero.ieResponsibilitiesRepresenting Quality function in Site Management meetings as required.Acting as a delegate for the Quality Lead.Act as Quality Systems Software Validation Lead for site.Leading and implementing significant process improvements, projects and cost saving initiatives using data & quality...

RequirementsBachelor's Degree or higher in Engineering or Science related fieldMinimum of five years' experience working in regulated environments such as medical device, FDA or ISO 13485 registered work environmentsStrong knowledge and experience of software lifecycle management tools such as JIRA, Qtest and VERAExperience with audit and regulatory...

Job DescriptionThis is a unique opportunity to join a global medical device organization as their software validation site lead. As a software quality assurance specialist, you will play a critical role in ensuring compliance with FDA and ISO 13485 regulations.Key Responsibilities:Lead software validation activities, including development and maintenance of...

Medtronic At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.  Our Purpose  At our Manufacturing Facility, we focus on meeting customer and patient needs every day. Our focus is on delivering the highest levels of quality products to our...

Job DescriptionThe role of Senior Quality Systems Engineer at HERO Recruitment is to provide technical guidance and leadership in the implementation of quality systems and processes within a regulated environment. This includes acting as a delegate for the Quality Lead, representing the Quality function in Site Management meetings, and leading investigations...

As a Software Validation Engineer, you will join a Global Medical Device organisation as their Software Validation site lead, sitting in and supported by a strong and tenured Quality function.Your day to day;Lead Software Validation Activities: Own and drive the validation of quality and manufacturing software systems to ensure compliance with FDA, ISO...

Direct message the job poster from HERO RecruitmentPrincipal Recruitment Consultant - Contact STEM@hero.ie or call 0868395533As a Software Validation Engineer, you will join a Global Medical Device organisation as their Software Validation site lead, sitting in and supported by a strong and tenured Quality function.Your day to day;Lead Software Validation...

Job OverviewAs a global leader in medical technologies, Teleflex is driven by its purpose to improve the health and quality of people's lives. Through its vision to become the most trusted partner in healthcare, it offers a diverse portfolio with solutions in various therapy areas. We believe that the potential of great people, purpose-driven innovation, and...

Required Skills and QualificationsTo be successful in this role, you will require:Bachelor's Degree or higher in Engineering or Science related field.Five (5) years' experience working in a regulated environments, specifically medical device, FDA or ISO 13485 registered work environments.Lead Auditor or Internal Auditor certification an advantage.

**Requirements:**To succeed in this role, the ideal candidate will possess a Bachelor's Degree or higher in Engineering, Computer Science, or a related field, and at least five years of experience working in a regulated environment, specifically in medical devices, FDA, or ISO 13485-registered industries. Familiarity with JIRA, Qtest, VERA, Oracle,...