We are looking for a skilled skilled with 4 to 8 years of experience in Regulatory Affairs, preferably with hands-on experience in Europe/ROW Regulatory Affairs. The ideal candidate should have a strong educational background in M. Pharma or B. Pharma and be based at our corporate office in KPHB.
Roles and Responsibility
- Develop and implement regulatory strategies for successful product approvals.
- Prepare and review regulatory submissions, including applications and reports.
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
- Conduct thorough reviews of regulatory documents to identify areas for improvement.
- Provide guidance on regulatory matters to internal stakeholders.
- Stay updated with changing regulatory requirements and industry trends.
Job Requirements
- Strong knowledge of regulatory affairs principles and practices.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Strong analytical and problem-solving skills.
- Proficient in MS Office and other relevant software.
- Experience working with regulatory authorities and industry partners.
- Qualification: M. Pharma / B. Pharma.
- Location: JEPL Corporate Office, KPHB.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.