Medical Device QA & Regulatory Compliance Lead

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.

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