.. every service associated with your packaging project. From concept through to design, development, production, inspection and logistics, our capabilities touch all bases. As a global organization with regional manufacturing and logistics sites in Europe, North America, and Asia, we have created an infrastructure .. read more
Job DescriptionBased in North Cambridgeshire, this is an exciting opportunity to join a MedTech company focused on the development of IoT medical wearable technology.
The company are hoping for someone to start quickly and they have a great product that can really support people in a range of environments.
This role can also be full time or part time, so it really is a unique opportunity.The Regulatory Manager will be responsible for internal and regulatory audits, which will include ATEX, FDA and CE Medical Devices, they will also need to manage the technical file.The successful candidate will have a good background in Medical Regulator Approvals within either BioTech or MedTech, along with some experience in Management.
Along with:* Experience with internal and regulatory audits* ATEX, FDA and CE Medical DevicesAs mentioned this role can be full time or part time, salary will not reflect this.
The company also offers excellent benefits and bonus.We are also looking for a regulatory manager who has experience with internal and regulatory audits, atex, fda and CE medical devices.
They need to be able to manage technical file.
They would ideally be able to start within 6 weeks also.
Salary £50K FTE but could be part time.
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