16 Sep
|
Maven Profcon Services
|
India
16 Sep
Maven Profcon Services
India
Prepare and review regulatory submissions, including technical documentation and clinical trial applications.
Conduct thorough analysis of regulatory requirements and ensure compliance with EU MDR 2017/745 standards.
Collaborate with cross-functional teams to develop and implement regulatory strategies.
Develop and maintain relationships with regulatory authorities and other stakeholders.
Stay up-to-date with changing regulatory requirements and industry trends.
Provide training and guidance to junior staff members on regulatory matters.
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📌 Junior Regulatory Executive Ahmedabad (India)
🏢 Maven Profcon Services
📍 India