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Fuze Health

Digital health platform enabling care access

Document Controller

Regulatory & Quality (Life Sciences)Updated on Nov 12
Full-timeDublin, Ireland

About the Job

Requirements

  • A bachelor's degree is required.
  • One to two years of experience in document control and change control within the medical device or pharmaceutical industry is required.
  • A basic understanding of ISO 13485:2016 and FDA 21 CFR Part 820 is required.
  • Strong attention to detail is required to maintain accurate documentation and comprehensive change control records.
  • Analytical skills are required to assess proposed changes and identify potential risks or conflicts within Quality Management System documentation.
  • Organisational and time management skills are required to manage competing priorities and work with minimal supervision.
  • Written and verbal communication skills are required to collaborate across functions and escalate issues appropriately.
  • The ability to adapt to changing priorities and business requirements is required.

Responsibilities

  • Own and coordinate document control and change control activities within the electronic Quality Management System.
  • Ensure Quality Management System changes are recorded, assessed and approved through the change control process before implementation.
  • Develop and maintain work instructions supporting effective document control and change control processes.
  • Coordinate meetings with process owners to review proposed changes, assess their impact and agree required actions.
  • Organise change control review meetings, track outstanding actions and support achievement of process key performance indicators.
  • Review document submissions for accuracy and completeness and route them to appropriate reviewers and approvers.
  • Confirm required approvals and applicable training are completed before documents are published.
  • Work with department managers and process owners to identify training requirements arising from new or revised documents and processes.
  • Maintain role-based training requirements and matrices in collaboration with the Quality Manager and relevant department managers.
  • Deliver Quality Management System induction training and onboard new employees to the electronic Quality Management System.
  • Maintain accurate, complete and traceable quality records within the Quality Management System.
  • Support review of products, processes and quality documentation against applicable regulatory and quality requirements.
  • Escalate overdue actions, documentation issues and potential compliance risks to the Quality Manager and relevant stakeholders.

Desired Qualifications

  • A degree in Science, Engineering or a related discipline is desirable.
  • Experience using an electronic Quality Management System to manage controlled documents, change controls and training records is desirable.
  • Familiarity with EU MDR 2017/745, EU IVDR 2017/746 and ISO 14971 is desirable.

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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