Regulatory Affairs Specialist
1 week ago
The Regulatory Affairs Specialist - Medical Devices will be responsible for preparing and submitting regulatory approval applications, ensuring compliance with medical device standards and regulations, and maintaining technical documentation for regulatory purposes. This role is ideal for recent graduates with backgrounds in engineering, science, or law who are eager to start a career in a stable and growing industry.
About the Role
This Medical Devices Regulatory Analyst position offers valuable training and guidance to help you build a rewarding long-term career in Regulatory Affairs. As part of a small team, you'll have the opportunity to learn from industry experts and contribute to obtaining regulatory approvals on a global scale.
Responsibilities
- Preparing and submitting regulatory approval applications.
- Ensuring compliance with medical device standards and regulations.
- Maintaining technical documentation for regulatory purposes.
- Providing administrative support for technical functions across the business.
Requirements
A degree in an engineering, science, or law-related field is required. Strong attention to detail and a desire to build a career in regulatory affairs are also essential. With a competitive salary range of £40,000 - £60,000 per annum, this role provides a unique opportunity for career growth and development.
Benefits
The company offers flexible remote work options and a supportive environment within a company that has an outstanding reputation within its niche industry. Note that the office is closed on Fridays, so suitable space for remote work on that day is necessary.
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