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Advanov Pharma is Ahmedabad based fastest growing IPR based Pharmaceutical company having its presence in Latin America, Brazil, CIS, MENA region, Africa, South Africa Asia and part of EU. we are having commercial operations in more then 18 Countries and around 15 Countries are under various stage of product registration.
Role & Responsibility:
minimum knowledge of CTD, ACTD,ECTD filing and in depth knowledge of dossier filing in various part of world.
1. Develop and implement regulatory strategies to ensure compliance with local and international regulations and guidelines for pharmaceutical products.
2. preparation and submission of dossiers, including ,drug applications, variations, renewals etc.
3. Stay updated on changes in regulatory requirements and communicate these changes to relevant stakeholders within the company.
4. Coordinate with cross-functional teams, including R&D, quality assurance, and marketing, to ensure regulatory compliance throughout the product lifecycle.
5. Provide regulatory input for product development, including reviewing and approving labeling, packaging, and promotional materials.
Qualification & Work Experience:
B Pharm, M Pharm with minimum 1-3 Years of Experience in Regulatory affairs,
Candidate from Ahmedabad only apply Only RA Experienced candidates considered QA /QC candidates are not preferred so please don't apply
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Date Posted: 19/06/2024
Job ID: 82247025