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Medical Devices Auditor - QMS

BSI Companies

United Kingdom

Hybrid

GBP 40,000 - 70,000

30+ days ago

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Job summary

Join a pioneering organization as a Medical Devices Auditor, where your expertise will help ensure patient safety and regulatory compliance across various medical devices. This role offers a unique opportunity to travel within EMEA, conducting audits that uphold the highest standards of quality management systems. With comprehensive training in ISO 13485 and MDSAP, you'll grow into a key player in the auditing process, working both independently and as part of a team. Be part of a legacy that has shaped national standards for over a century, and contribute to a mission of excellence in healthcare technology.

Qualifications

  • 4+ years experience in medical device sectors including design, R&D, or manufacturing.
  • 2+ years working with quality management systems.

Responsibilities

  • Conduct audits on-site, remotely, or hybrid after training.
  • Write reports and manage client audit schedules.

Skills

ISO 13485

MDSAP

Medical Device Regulation (MDR)

Quality Management Systems

Research and Development

Manufacturing or Production

Education

BSc in Biology or Microbiology

MSc in Chemistry or Biochemistry

PhD in Engineering or Bioengineering

Tools

Audit Tools

Reporting Software

Job description

Medical Devices Auditor - QMS

Location: UK - field-based, 70%-75% of travel required within EMEA

We’re looking for talented people to join our medical device auditor team. The role involves travelling to various locations to assess quality management systems, supporting patient safety and regulatory compliance. Our audits encompass standards such as ISO 9001 / ISO 13485 and schemes such as MDSAP. We also support conformity assessment activities such as those related to UKCA and CE marking.

Responsibilities:

In the first six months of being a Client Manager, you will:

  1. Be given training in ISO 13485 Lead Auditor training, MDSAP (Medical Device Single Audit Programme) and MDR (Medical Device Regulation)
  2. Initially observe how audits are conducted but then grow to conduct them on an individual basis

In a typical week after being fully trained, you will:

  1. Conduct an audit on site, remotely or hybrid, working alone or as part of a team
  2. Write up your reports and liaise with the planning team and delivery manager to manage your clients and audit schedule
  3. Complete other administrative activities as required

Minimum Requirements:

To be successful you need to have a minimum of 4 years hands-on experience in one or more of the following areas:

  1. Research and development
  2. Design or design development
  3. Servicing, maintenance and/or testing
  4. Manufacturing or production experience

Covering a range of medical devices which could include:

  1. Active devices: X-rays, Heart Lung machines, Defibrillators, MRI Scanners
  2. IVD (invitro diagnostics) instrumentation and/or reagents
  3. Active Implantable Medical Devices: Cochlear Implants, MEMS systems, Implantable infusion pumps, including Software as a Medical Device
  4. Orthopaedics - spinal implants, bone/dental cements, cartilage, and soft tissue repair
  5. Wound and skin care - dressings, foams, gels

Your experience will also include at least 2 years' working with quality management systems.

You must have completed a university or technical college degree or equivalent in a related STEM subject (BSc, MSc or PhD) such as: Biology or Microbiology, Chemistry or Biochemistry, Computer and Software Technology, Electrical, Electronic, Mechanical, or Bioengineering, Human Physiology, Medicine, Pharmacy, Physics or Biophysics.

Do you believe the world deserves excellence?

Headquartered in London, BSI is the world's first national standards organization with more than 100 years of experience. If you want to contribute to this inspiring challenge, bring your open and enthusiastic mindset to our dynamic team, apply now and become part of the BSI family!

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