Job Description

Responsibilities:
- Prepare and submit regulatory documents to health authorities.
- Monitor compliance with local and international regulations.
- Liaise with regulatory bodies to facilitate approval processes.
- Collaborate with cross-functional teams on product development.
- Conduct regulatory impact assessments on changes in legislation.

Requirements & Skills

- Strong knowledge of pharmaceutical regulations and guidelines.
- Excellent communication and interpersonal skills.
- Detail-oriented with exceptional organizational abilities.
- Proficient in data analysis and document preparation.
- Ability to work independently and in a team environment.