Medical Device QA & Regulatory Compliance Lead
Listed on 2026-09-29
-
Healthcare
Medical Science -
Quality Assurance - QA/QC
Otsuka Pharmaceutical Co., Ltd in the United Kingdom is seeking a Quality Assurance professional to develop and manage compliance with ISO 13485 and other applicable standards. The role involves acting as Post Marketing Surveillance Manager and supporting regulatory compliance initiatives.
Ideal candidates will have experience in quality management systems and regulatory frameworks, along with the ability to conduct training and manage complaints efficiently. This position offers a unique opportunity to contribute to Otsuka's commitment to quality in the medical device sector.
Join us at Otsuka Pharmaceutical Co., Ltd as our next Medical Device QA & Regulatory Compliance Lead in United Kingdom.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).