Quality Engineer - Fuze Services - Fixed Term Contract

LetsGetChecked; United States; On-site; USD 70,000 - 79,000; Full time

Benefits offered by this job

Health insurance

Employee Assistance Programme

Pension

Annual compensation reviews

Referral bonus programme

Internal opportunities and careersClin

Leave policy (maternity/paternity/Par.

Job summary

Fuze Health’s Dublin facility seeks a detail-oriented Quality Engineer to ensure medical device compliance with ISO 13485, 21 CFR Part 820, MDR, IVDR, and ISO 14971. You will support change controls, validations, audits, risk management, and cross‑functional teams to maintain product quality and patient safety.

This 12-month fixed-term, onsite role offers competitive compensation and diverse benefits within a collaborative environment.

Qualifications

• Bachelor’s degree in Biomedical Engineering, Quality Management, or related field.
• 2–5 years in quality within medical devices.
• Experience with ISO 13485, 21 CFR Part 820, MDR 2017/745, IVDR 2017/746, ISO 14971, IEC 62366, GAMP5.
• Audits experience (internal/external) a plus; post‑market surveillance knowledge preferred.
• Statistical methods; Lean/Six Sigma; Minitab experience advantageous.
• Strong communication, technical writing, and cross‑functional collaboration.

Responsibilities

• Evaluate current products/processes for regulatory compliance.
• Review/change controls and assist through the change process.
• Approve validation deliverables for equipment and processes.
• Support internal/external audits and resolve findings.
• Lead risk management, maintain docs, assess mitigations.
• Collaborate with cross‑functional teams on changes and automation.
• Handle customer complaints and implement corrective actions.
• Investigate CAPAs and non‑conformances; draft required records.
• Stay updated on regulatory changes and best practices.

Skills

Regulatory compliance

ISO 13485

Six Sigma

Lean

Minitab

SAP QM

Root cause analysis

Technical writing

Cross-functional

Quality culture

Education

Bachelor’s in Biomedical Engineering/Quality Management

Master’s degree advantageous

Tools

SAP S/4HANA QM

GAMP5

Job description

Job Summary

At Fuze Health, we put patients first and tirelessly address the most pressing needs in healthcare. We empower millions to digitally connect with care providers, essential health resources and needed treatments – and enable care providers, employers, health plans and life sciences companies to meaningfully enhance quality, outcomes and value. We are dedicated to helping our partners evolve and modernize to meet emerging patient and marketplace needs. Fuze Health’s foundation is built upon the strategic combination of several proven, technology-powered innovators in the digital health, diagnostics, and pharmacy sectors. Our growing portfolio brings together the capabilities of industry leaders including LetsGetChecked, Truepill, and Alto Pharmacy, to create a distinctive, unified force in healthcare. Together, we have the shared vision, advanced capabilities and talented teams to deliver next‑generation solutions that patients and healthcare partners need today and into the future.

Quality Engineer - Fuze Services

We are seeking a detail‑oriented Quality Engineer to join our dynamic team at our Manufacturing Facility in Dublin to ensure our products and processes comply with relevant regulations and standards, including ISO 13485, 21 CFR Part 820, MDR 2017/745, IVDR 2017/746, and ISO 14971. This role involves supporting change controls, participating and reviewing validations related to manufacturing equipment and processes, supporting and contributing to internal and external audits, leads risk management activities, and collaborating closely with the teams involved in the product life cycle.

This is a 12 Months Fixed Term Contract, based onsite in our Dublin 11 facility.

Job Description

Responsibilities

• Evaluate current products and processes to ensure ongoing compliance with applicable regulations and standards such as ISO 13485, 21 CFR Part 820, MDR 2017/745, IVDR 2017/746, and ISO 14971
• Review and support change controls/design changes, assisting the team through the change process to maintain compliance.
• Review and approval of validation deliverables for equipment and processes, and assist in implementing effective process controls.
• Participate in internal and external audits, supporting audit preparation and the resolution of audit findings by liaising with process owners and managers.
• Lead risk management activities, maintain risk management documentation, and help assess risk mitigation techniques, potential failure modes, defect frequency, severity, and process controls.
• Collaborate with cross‑functional teams to implement changes and automated systems with efficiency and accuracy.
• Responsible for customer complaint handling including the implementation and follow up of corrective actions
• Assist in analysing and summarising potential issues by assessing the impact on customer safety and product quality, and contribute to decisions related to the disposition of non‑conforming product.
• Support the investigation of CAPAs and non‑conformances, drafting and reviewing applicable records and documentation for completion at critical phases.
• Stay updated on regulatory changes and industry best practices, integrating quality into all aspects of work, and offering problem‑solving recommendations to the operations and engineering teams.

What are we looking for?

• Experience: 2–5 years of relevant experience in a quality department within the medical device industry.
• Education: Bachelor’s degree in Biomedical Engineering, Quality Management, or relevant disciplines (a Master’s degree is an advantage).
• Working knowledge of ISO 13485, 21 CFR Part 820, MDR 2017/745, IVDR 2017/746, ISO 14971, IEC 62366, GAMP5, and other applicable industry standards & regulations.
• Experience supporting new product introductions (Class II medical devices, Class A IVDs, Procedure Packs) and knowledge of manufacturing engineering, risk analysis, and documenting risk management files/reports.
• Exposure to supplier, internal, and external audits (a professional certification in auditing is a plus).
• Experience reviewing technical documentation, assisting in assessing the impact of proposed changes on the QMS, and supporting post‑market surveillance activities by working constructively with stakeholders.
• Knowledge of root cause analysis, continuous improvement activities, and execution/verification of effectiveness.
• Familiarity with Statistics, Lean, and Six Sigma methodologies; Minitab experience is an advantage.
• Strong organizational skills with the ability to support project management initiatives and foster a positive work environment.
• Ability to work effectively in a fast‑paced medical device manufacturing environment, multi‑task, and prioritise tasks to meet high expectations and tight deadlines.
• Culture: Ability to work well within cross‑functional teams and promote a ‘Quality Culture’ where compliance is viewed as a competitive advantage.
• Experience using ERP systems such as SAP S/4 HANA (Quality Management [QM] module preferred).
• Strong analytical, troubleshooting, process improvement, technical writing, and verbal communication skills.

Additional Information

Salary and Benefits

Salary Range: €60,000 - €68,000

Benefits - Fuze Health

• Health insurance and an Employee Assistance Programme
• Pension
• Annual Compensation Reviews
• A referral bonus programme to reward you for helping us hire the best talent
• Internal Opportunities and Careers Clinics to help you progress your career within the company
• Maternity, Paternity, Parental and Wedding leave
• LetsGetChecked has a flexible annual leave policy

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Equal Opportunity Employer

Fuze Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, gender identity, sexual orientation, age, disability, veteran status, or any other legally protected basis. If you have a disability and require reasonable accommodation during any portion of the application or hiring process, please contact us at [e-mail].

Fuze Health considers qualified applicants with arrest or conviction records for employment and conducts background checks consistent with applicable law, including the California, Los Angeles County, San Francisco, Philadelphia, and New York City Fair Chance laws. We are an E‑Verify participating company.

Use of Automated Decision Tools

Fuze Health recruiters and hiring managers may use automated decision tools to help identify candidates who match the stated job requirements, and to what extent. These tools are designed to help ensure fairness in all aspects of the hiring process by providing recruiters and hiring managers with data‑backed insights based on information provided in your resume, including work experience, education, and other skills. Fuze Health does not use automated decision tools to make hiring decisions; hiring decisions always involve human review and input. If you have any questions or would like to request an alternative process, please contact us at [e-mail].

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