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Fuze Health

Digital health platform enabling care access

Quality Engineer

Validation, Compliance & Quality SystemsPosted on Nov 10
Full-timeDublin, Ireland

About the Job

Requirements

  • A bachelor's degree in Biomedical Engineering, Quality Management, or a relevant discipline is required; a master's degree is an advantage.
  • Two to five years of relevant experience in a quality department within the medical device industry.
  • 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 and regulations.
  • Experience supporting new product introductions for Class II medical devices, Class A in vitro diagnostic devices, and procedure packs; knowledge of manufacturing engineering, risk analysis, and documenting risk management files and reports.
  • Exposure to supplier, internal, and external audits; auditing certification is a plus.
  • Experience reviewing technical documentation, assessing the impact of proposed changes on the quality management system, and supporting post-market surveillance while working constructively with stakeholders.
  • Knowledge of root cause analysis, continuous improvement activities, and execution and verification of effectiveness.
  • Strong analytical, troubleshooting, process improvement, technical writing, and verbal communication skills.
  • Ability to support project management initiatives and work effectively in a fast-paced medical device manufacturing environment, multitask, and prioritize tasks to meet deadlines.
  • Familiarity with statistics, Lean, and Six Sigma methodologies; Minitab experience is an advantage.
  • Experience using enterprise resource planning systems such as SAP S/4HANA; the Quality Management module is preferred.
  • Ability to work effectively within cross-functional teams and promote a quality culture.

Responsibilities

  • Evaluate current products and processes to ensure ongoing compliance with applicable regulations and standards, including ISO 13485, 21 CFR Part 820, MDR 2017/745, IVDR 2017/746, and ISO 14971.
  • Review and support change controls and design changes, assisting the team through the change process to maintain compliance.
  • Review and approve validation deliverables for equipment and processes, and assist in implementing effective process controls.
  • Participate in internal and external audits, support audit preparation, and resolve 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 and severity, and process controls.
  • Collaborate with cross-functional teams to implement changes and automated systems efficiently and accurately.
  • Handle customer complaints, including implementing and following up on corrective actions.
  • Analyze and summarize potential issues by assessing their impact on customer safety and product quality, and contribute to decisions about the disposition of non-conforming products.
  • Support investigations of corrective and preventive actions and non-conformances, drafting and reviewing applicable records and documentation for completion at critical phases.
  • Stay updated on regulatory changes and industry best practices, integrate quality into all aspects of work, and offer problem-solving recommendations to operations and engineering teams.

Desired Qualifications

  • A master's degree is an advantage.
  • A professional certification in auditing is a plus.
  • Experience with Minitab is an advantage.
  • Experience with the SAP S/4HANA Quality Management module is preferred.

About the Company

Fuze Health

Digital health platform enabling care access

Fuze Health runs a digital health platform that connects patients with care providers, health resources, and treatments, while serving healthcare partners like providers, employers, health plans, and life sciences companies. Its products work by linking patients to providers and resources through digital tools and services, including virtual pharmacy and at‑home health options, to personalize and improve care. The company differentiates itself through its large scale and integrated assets from a merger between Truepill and LetsGetChecked, with Alto joining, enabling more therapies and care delivered in more locations, including at home. Its goal is to reach more patients with more therapies in more places, while protecting personal data and using it only to respond to inquiries, support customers, and improve services.

Company size
201-500
Company stage
Not listed
Total funding
Not listed
Headquarters
San Francisco, CA
Founded
Not listed

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