I'm a dedicated Regulatory Affairs Officer with a Strong background in medical Device Industry. I excel in navigating complex regulatory landscapes, ensuring compliance with industry standards, and streamlining approval processes. With a proven track record of successfully bringing Medical devices to market, I am committed to maintaining the highest Quality Standards while facilitating innovation. I thrive in dynamic environments, leveraging my expertise to facilitate seamless product approvals and contribute to the growth of healthcare organizations.
Master of Biotechnology
Perform lab Safety Techniques & Maintain Qc
Prepare and Monitored Media Culture
DNA extraction & Isolation
Report Writing
Regulatory Knowledge
Submission & Approval
Quality Assurance
Compliances
outside of my professional life in Regulatory Affairs within Medical Device Industry, I'm an Individual with a diverse set of interests that complement my skillset. health & wellness are paramount to me, as I regularly engage in activities like Yoga & Meditation to maintain a balanced Lifestyle. My passion for continuous Learning extends beyond my work, as I enjoy staying up-to-date with industry trends and regulatory updates through avid reading of Medical journals and related Publications. Furthermore, I find immense satisfaction in contributing to my community by volunteering for Healthcare-related causes. Travelling has not only broadened my horizons but also sharpened my adaptability skills, which are invaluable in dynamic field like regulatory Affairs. I'm also a strong believer in precision and attention to detail, traits that translate well into my hobbies, such as puzzel-solving and cooking. overall, my interests reflect my commitment to health, lifelong learning, Community engagement, and the pursuit of Excellence in both my personal and professional endeavors
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