Senior Regulatory Affairs Specialist

16 hours ago

Singapore beBeeRegulatory Full time

Job Title: Senior Regulatory Affairs Specialist">As a key member of the regulatory team, you will be responsible for developing and implementing regulatory strategies for medical devices and therapeutic products. Your primary focus will be on ensuring compliance with relevant regulations and maintaining accurate and up-to-date records.The ideal candidate will have a strong understanding of regulatory affairs and be able to work collaboratively with cross-functional teams to achieve business objectives. You will be responsible for managing regulatory files, conducting regulatory monitoring, and evaluating the effects of amendments or changes.Key Responsibilities:• Develop and implement regulatory strategies for medical devices and therapeutic products• Manage regulatory files and maintain accurate and up-to-date records• Conduct regulatory monitoring and evaluate the effects of amendments or changes• Collaborate with cross-functional teams to achieve business objectives• Ensure compliance with relevant regulations and standardsRequirements:• Well-versed in regulatory affairs and experience in medical device registration• Strong communication and negotiation skills• Ability to multitask effectively in a fast-paced environment• Flexibility and ability to adapt to change• Good team player and self-motivated• B-Pharm (preferred) or equivalent qualification• Minimum 4 years of relevant experience in medical device industryBenefits:• Competitive salary and benefits package• Opportunity to work with a dynamic and growing company• Collaborative and supportive work environment• Professional development opportunitiesOther Information:• Vantive is an equal opportunities employer• We are committed to working with and providing reasonable accommodations to individuals with disabilities globally

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