Expert Global Regulatory Affairs Professional

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hubballi, India beBeeRegulatory Full time

Senior Regulatory Affairs AssociateAs a senior regulatory affairs professional, you will play a pivotal role in the registration and lifecycle management of various biological products in multiple markets.Main Responsibilities:Global Regulatory Submissions: Prepare and review Marketing Authorization Applications & Variations for filing in various countries.Strategic Compliance: Contribute to the preparation of regulatory submissions from a global and regional perspective.Regulatory Intelligence: Develop a strong understanding of regulatory frameworks and trends across regions.Cross-Functional Collaboration: Collaborate with cross-functional teams to ensure compliance with global pharmaceutical legislation and guidance.This role requires a proactive and results-driven individual who can effectively manage competing priorities and meet deadlines. You will have the opportunity to work closely with a talented team of professionals and contribute to the success of our organization.Required Skills and Qualifications:Strong Knowledge: In-depth knowledge of regulatory frameworks, guidelines, and regulations.Excellent Communication: Effective communication and interpersonal skills.Project Management: Proven ability to manage multiple projects simultaneously and prioritize tasks.Critical Thinking: Strong analytical and problem-solving skills.We offer a dynamic and supportive work environment that fosters growth and development. If you are a motivated and detail-oriented individual who is passionate about regulatory affairs, we encourage you to apply for this exciting opportunity.

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