associate Regulatory Affairs specialistMedtronic

Careers that Change Lives We're a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Join our team in (Clinical Affairs, Regulatory Affairs, Medical Affairs) and help shape policies that change lives. Work with us to incentivize better patient care, and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide. A Day in the Life Responsibilities may include the following and other duties may be assigned. Execute submission strategy. Performs coordination and preparation of document packages for regulatory submissions for Global Region Leads or compiles all materials required in submissions, license renewal and annual registrations. Monitors and improves tracking / control systems. Keeps abreast of regulatory procedures and changes. Recommends strategies for earliest possible approvals of clinical trials applications. Provide on-time status about projects under their scope and all applicable regulatory activities assigned. Must Have: Bachelor's Degree required. 0 years of experience required. Your Profile Bachelor's degree in Pharmaceutical Sciences, Industrial Engineering, Biomedical Engineering, or field related experience is an advantage. At least 1-year regulatory experience in medical devices is highly appreciated. High proficiency in Microsoft tools Excellent communication skills Databases management, document interpretation, queries, and workflow skills. Strategic thinking, analytical and problem-solving skills, decision making skills.
foundit

Taguig City, Metro Manila
Permanent
Full-time