Science Medical jobs in Galway, County Galway
- MedtronicGalway, County Galway
- At our Sterilisation Validation Department in Medtronic, plc, we focus on product quality excellence and providing exemplary service to the businesses &…
- Galway Biomedical LtdBallybrit, County Galway
- Knowledge of ISO13485, EU MDR, FDA QMSR and applicable medical device requirements.
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- Vita Global SciencesGalway, County Galway
- Clinical/medical background is a plus.
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- Boston ScientificGalway, County Galway
- Hons Bachelor Degree (Level 8) in engineering or science is essential.
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- Luminate MedicalGalway, County Galway
- Experience with medical device trials (IDE SR/NSR, De Novo, 510(k)).
- MD/PhD/PharmD or equivalent in life sciences, medicine, or related field with demonstrated…
- Luminate MedicalGalway, County Galway
- Experience with medical device trials (IDE SR/NSR, De Novo, 510(k)).
- MD/PhD/PharmD or equivalent in life sciences, medicine, or related field with demonstrated…
- MedtronicGalway, County Galway
- At our Quality Department in Medtronic, plc, we focus on supporting the product value stream to ensure that customer and patient needs are met every day.
- View all Medtronic jobs - Galway jobs - Quality Engineer jobs in Galway, County Galway
- Salary Search: Quality Engineer I salaries in Galway, County Galway
- See popular questions & answers about Medtronic
- Boston ScientificGalway, County Galway
- Hons Bachelor Degree (Level 8) in engineering or science is essential.
- Interest in medical technology, manufacturing, product development or continuous…
- CPLGalway, County Galway
- Bachelor’s degree in science, Engineering, Quality, Life Sciences, or a related discipline.
- Working Hours: 40 hours per week.
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- ViatrisGalway, County Galway
- Bachelor's degree (or equivalent) in a science-related discipline.
- Develop and implement global CMC regulatory strategies for injectable products.
- Freudenberg Medical Ireland Ltd.Spiddal, County Galway
- Good working knowledge of ISO 13485, FDA requirements and medical device Quality Systems.
- Health Insurance: Rely on comprehensive services whenever you need it.
- Boston ScientificGalway, County Galway
- The shift for this position is Nights.
- You will demonstrate commitment to the Quality Policy through your daily execution of sound quality practices and the…
- Caragh PrecisionGalway, County Galway
- Previous Quality Control or Quality Inspection experience within the medical device industry.
- Perform visual inspections of medical device components and…
- ICS Medical DevicesGalway, County Galway
- Research and assess emerging technologies for medical device applications.
- Produce clear technical documentation aligned with medical device regulatory…
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- LUMA VisionGalway, County Galway
- Support RD/NPI activities at our contract manufacturing site, on site 4 days a week.
- Design and develop mechanical components, sub-assemblies and large…
- MedtronicGalway, County Galway
- Experience in development and sustaining of medical devices.
- As a Senior Released Product Engineer, you will be a member of the Operations team working within…
Quality Engineer 1 - Sterilization Validation
Quality Engineer 1 - Sterilization Validation
Job details
Full job description
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
At our Sterilisation Validation Department in Medtronic, plc, we focus on product quality excellence and providing exemplary service to the businesses & operating units we support. Our Sterilisation Quality Engineers anticipate and respond tochanging sterility requirements, provide strategic leadership to influence the
global sterility environment to benefit the patients we serve and are directly
involved in building the organisation in support of Sterility Assurance assessments for New Product Development and site transfers.
- Support routine Sterility Assurance activities e.g GMP, Standards Compliance, Cleanroom Risk Assessment, Limits review, Dose Audit activity, Cycle Requalification, Supplier Change control etc.
- Support Sterility Assurance activities for new products and change control, developing strong partnering relationships with these groups, at both manufacturing and design sites.
- Participate in root cause investigations and continuous improvement in day-to-day activity, initiating appropriate corrective actions and following through to implementation.
- Support cross functional teams in design protocols to ensure that new products/product changes are adequately evaluated/tested to guarantee compliance to all regulatory standards.
- Deliver on projects assigned and works with other stakeholders to achieve desired results within defined timeframes.
- Support your projects in internal and external audits and in submission preparation, addressing any questions regarding these submissions.
- Perform calculations, technical and record keeping duties in conformance with company and regulatory policies and standards to meet quality and accuracy requirements.
- Review systems and processes for optimisation and troubleshooting. • Adhere to all relevant site wide procedures and practices for Safety & GMP.
Key Skills & Experience
- Minimum Level 7 degree in a relevant technical discipline e.g. Science or Engineering.
- 1-2 years’ experience with Sterilisation Validation/Microbiology is desirable.
- Excellent understanding of GMP and documentation required.
- Dynamic team player with good communication skills. Can work effectively and proactively as an individual or on cross functional teams.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com .
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
The final salary within this range will be determined based on objective, job-related criteria, including relevant experience, skills and qualifications, in accordance with our compensation framework. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).