Key Responsibilities
- Prepare and submit regulatory dossiers for emerging markets, including Brazil, China, and LATAM.
- Participate in deficiency meetings, review pending deficiencies, and collaborate with cross-functional teams to ensure timely submission of responses.
- Manage and evaluate international regulatory projects in alignment with company goals.
- Plan, coordinate, and submit regulatory dossiers and responses in regulated markets.
- Review documents, identify gaps, ensure compliance, and facilitate acceptance meetings.
- Plan amendments, updates, and annual reports, ensuring accurate compilation, review, and submission.
Qualifications & Skills
Bachelor's or Master's degree in Pharmacy, Life Sciences, or a related field.3-8 years of experience in regulatory affairs within the API / pharmaceutical industry.Understanding of global regulatory requirements, dossier preparation, and submission processes.Strong analytical skills to identify and resolve regulatory gaps.Ability to collaborate with internal teams and regulatory authorities effectively.Experience in handling multiple regulatory projects and ensuring timely submissions.Skills Required
Regulatory, Api, Compliance, Regulatory Affairs, annual planning