Regulatory Affairs Specialist for Medical Device Compliance
3 days ago
Yolk Recruitment Ltd is partnering with a growing medical device manufacturer to find a skilled Regulatory contractor.
This part-time opportunity, requiring 2-3 days of work per week, involves supporting the company's regulatory activities, including worldwide submissions, standards database management, and compliant procedure creation.
The ideal candidate will have previous experience in Medical Devices Regulatory Affairs and knowledge of various regulatory frameworks, such as UK MDR 2022, EU MDD, and ISO 13485.
A competitive salary of £40,000 - £50,000 per annum is offered for this role, reflecting the market rate for similar positions in the UK.
The location is based in the UK, with remote work options available due to the flexible nature of this contract position.
The successful applicant will be responsible for:
- Supporting worldwide regulatory submissions
- Reviewing and managing the company's standards database
- Advising on and implementing changes to technical files as required
- Contributing to the creation and implementation of compliant Regulatory procedures
The desired skills and qualifications include:
- Previous experience in Medical Devices Regulatory Affairs
- Knowledge of UK MDR 2022, EU MDD, and ISO 13485
- Familiarity with regulatory compliance and marking requirements
We are seeking an experienced professional who can effectively support our client's regulatory needs and contribute to their growth. If you are passionate about regulatory affairs and have the necessary skills and qualifications, please apply for this exciting opportunity.
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