BioTalent
Regulatory Specialist
Reading
Posted about 20 hours ago
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BioTalent is currently partnered exclusively with an SME Class 2 Device business who are looking to find their latest addition to their regulatory team
The role will give you:
- A chance to work across both NPD and NPI
- Work in global markets
- Support by a senior leader that BioTalent has had many years of working with
- Variety of tasks
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You will need to bring in:
- Minimum of 3 years of experience within regulatory affairs within Medical Devices or IVD
- Experienced working ISO 13485
- Hands on experience with technical file creation, MDR updates and some exposure to registrations
- Ideal candidates will have worked within global markets such as US or MDSAP countries
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If this role sounds interesting please apply or reach out on michael.kakoullis@biotalent.com or call +447833626032
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