Senior MedTech Regulatory & Quality Consultant
Astro Studios, Inc., Wendy, Cambridgeshire
Senior MedTech Regulatory & Quality Consultant
Salary not available. View on company website.
Astro Studios, Inc., Wendy, Cambridgeshire
- Full time
- Permanent
- Onsite working
Posted 1 week ago, 1 Jun | Get your application in now before you're too late!
Closing date: Closing date not specified
Job ref: 0ad623891e2e47c3ad3840729f0dff19
Location ref: Wendy, Cambridgeshire
Full Job Description
Senior MedTech Regulatory & Quality Consultant
Date posted: 2026-05-30T00:00:00
Location: Melbourn, Cambridgeshire, UK
Office/Area: SG8 6
Company: Astro Studios, Inc.
Astro Studios, Inc. is looking for a Medical Device Regulatory and Quality Consultant to join our dynamic Healthcare & Life Sciences consulting team in Melbourn, UK. This role involves providing regulatory and quality compliance expertise for medical devices and combination products. Candidates should have at least five years of experience in the MedTech field, a technical background, and a strong understanding of regulations.
Responsibilities
- Provide regulatory and quality compliance expertise for medical devices and combination products
- Prepare and maintain regulatory submissions and technical documentation
- Support post-market activities to ensure ongoing compliance
Requirements
- At least five years of experience in the MedTech field
- Technical background with strong understanding of regulations
Benefits
- Private healthcare
- Generous leave
- Pension scheme
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Astro Studios, Inc. is looking for a Medical Device Regulatory and Quality Consultant to join our dynamic Healthcare & Life Sciences consulting team in Melbourn, UK. This role involves providing regulatory and quality compliance expertise for medical devices and combination products. Candidates should have at least five years of experience in the MedTech field, a technical background, and a strong understanding of regulations. Benefits include private healthcare, generous leave, and a pension scheme.
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