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Are you passionate about regulatory affairs in the pharmaceutical and healthcare industry? Genedrift, a leading provider of regulatory and pharmacovigilance services, is hiring a Regulatory Affairs Executive in India for a fully remote position. This role is ideal for professionals with experience in regulatory documentation, dossier preparation, and compliance monitoring, seeking to grow in a dynamic and client-focused environment.
Key Responsibilities
As a Regulatory Affairs Executive at Genedrift, you will:
- Prepare, manage, and submit regulatory documentation and dossiers.
- Ensure compliance with local and international regulatory requirements.
- Monitor updates in regulatory guidelines and standards.
- Liaise with internal teams and external stakeholders to facilitate timely submissions.
- Support post-market surveillance and product safety activities.
- Maintain accurate records of regulatory affairs activities.
Required Qualifications
- Bachelor’s degree in Pharmacy, Life Sciences, or Regulatory Affairs.
- Experience in regulatory documentation and dossier preparation.
- Knowledge of regulatory compliance and requirements.
- Strong written and verbal communication skills.
- Attention to detail and strong organizational abilities.
- Ability to work independently and in a fully remote environment.
- Experience in the pharmaceutical or healthcare industry is a plus.
Benefits
- Fully remote work from anywhere in India.
- Opportunity to work with a leading regulatory and pharmacovigilance services provider.
- Exposure to international regulatory standards and documentation.
- Career growth and professional development in regulatory affairs.
How to Apply
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