Kinetica, Tyne And Wear, England, United Kingdom
Base pay range
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About the Company
We are looking for a quality professional with extensive experience in compliance for product development and design control, to work for a leading diagnostics company. This is a fully site-based role within a newly formed team.
Responsibilities
- Support site projects that drive new product development (NPD) and product lifecycle management (PLCM).
- Provide Design Control leadership and collaborate across LBS and Danaher sites.
- Improve processes to reduce variability and strengthen product robustness.
- Lead functional teams or medium-scale projects as needed.
- Partner with Regulatory Affairs on global submissions, including FDA 510(k), PMA, and IVDR CE documentation.
Requirements
- Strong knowledge of Design Controls and design/development practices for medical device or diagnostic products.
- Extensive experience in medical device development and quality systems.
- Expert understanding of standards such as 21 CFR 820, ISO 13485, ISO 14971, and MDSAP.
- Proven Quality leadership experience.
- Bachelor’s degree in a scientific, or technical discipline.
Seniority level
- Not Applicable
Employment type
- Full-time
Job function
- Quality Assurance and Research
Industries
- Medical Equipment Manufacturing
- Measuring and Control Instrument Manufacturing
- Biotechnology Research
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Contact Detail:
Kinetica Recruiting Team