This is a full-time on-site role for an International Regulatory Affairs professional. The role involves ensuring compliance with regulatory requirements and documentation related to pharmaceutical products. The candidate will be responsible for preparing and submitting regulatory submissions, and keeping up-to-date with changing regulations in different countries. The role will require collaboration with internal and external stakeholders to ensure the smooth flow of regulatory processes.
Key Responsibilities
- Ensure compliance with regulatory requirements and documentation related to pharmaceutical products.
- Prepare and submit regulatory submissions.
- Stay current with changing regulations in different countries.
- Collaborate with internal and external stakeholders to ensure the smooth flow of regulatory processes.
Qualifications
- Strong knowledge of Regulatory Affairs and compliance.
- Experience in preparing regulatory documentation.
- Familiarity with international regulatory requirements.
- Ability to navigate regulatory processes and submissions.
- Attention to detail and ability to analyze complex information.
- Strong communication and interpersonal skills.
- Experience in the pharmaceutical industry is preferred.
- Degree in Pharmacy, Regulatory Affairs, or a related field.
Skills
- Regulatory Affairs
- Regulatory Requirements
- Compliance
- Documentation Preparation
- Regulatory Submissions
- Interpersonal Communication
- Pharmaceutical Industry Experience
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