Quality Manager Medical Device jobs
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- GE HEALTHCAREMascot NSW 2020
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- Avance ClinicalRemote
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- CSL BehringBroadmeadows VIC
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- Department of HealthMelbourne City Centre VIC
- Demonstrated experience in healthcare clinical governance and/or quality improvement initiatives.
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- Novo NordiskSydney NSW
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- University of MelbourneParkville VIC 3010
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- ProductLife GroupAustralia
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- Queensland GovernmentBrisbane QLD
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- EnovisBrisbane QLD
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- Blackmores GroupBraeside VIC
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- ArcadisMelbourne VIC
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Job Post Details
Medical Device Auditor IVD ISO13485(home based) - job post
Job details
Job type
- Full-time
Location
Full job description
We exist to create positive change for people and the planet. Join us and make a difference too!
Position- Medical devices Auditor( IVD technical background preferred )
Location – New South Wales Australia (homebased)
Are you looking for a career where you can use your expertise to ensure patient safety?
Do you want variety and exposure to different medical device manufacturers and cultures?
Your next career could be as an auditor; or as we call them at BSI a Client Manager.
Our team in APAC are looking for medical device professionals who can demonstrate their expertise with design and/or manufacture or servicing of animal tissues in Medical Devices.
What will I do?
- Firstly, you’ll undertake extensive training to deliver in your role. This includes: ISO13485 Lead Auditor course, MDSAP (Medical Device Single Audit Programme), and MDR (Medical Device Regulation).
- Then as a Client Manager you’ll be responsible for frequently travelling across New Zealand and Australia and some International travel might be required.
- You’ll assess ISO13485 quality management systems and associated medical device regulatory requirements on customer sites or sometimes remotely, write up comprehensive reports and present these to the client.
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Experience with In Vitro Diagnostic (IVD) devices would be an advantage for this role.
To be a successful Auditor you’ll:
- Be degree educated (Bioscience or Biotechnology degree, Masters or equivalent qualifications)
- Your education must be in a discipline relevant to medical device manufacture and use and contain modules relating to implantable devices.
- Have a minimum of 5 years being directly responsible of either the design and development or research and development, of an array of different medical devices.
- Strong background in in-vitro diagnostic medical devices, including both reagents and instruments, and their interfaces (experience can be - research, design and development, manufacturing, or testing).
- This position is open to local candidates only. BSI does not provide sponsorship for work permits.
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