
Regulatory Affairs Officer
- Vadodara, Gujarat
- Permanent
- Full-time
- Strong understanding of regulatory compliance within international markets for diverse industries.
- Proficiency in navigating and applying FDA regulations to ensure business activities align with compliance standards.
- Experience with implementing and managing quality management systems in alignment with industry standards.
- Capability to prepare and manage regulatory submissions ensuring timely and accurate documentation.
- In-depth knowledge of product lifecycle management from initial development through end-of-life processes.
- Required experience with devising dossiers and supporting documentation for regulatory approvals.
- Familiarity with ROW regulations and requirements to maintain global compliance across various regions.
- Excellent communication skills to articulate regulatory requirements clearly to internal and external stakeholders.
- Proficiency in handling technical documents to facilitate accurate and timely submissions.
- Proven ability to review regulatory documents and submissions effectively, ensuring their accuracy and compliance.
- Strong analytical skills to assess regulatory data and provide critical insights for decision-making.
- Attention to detail to meticulously handle documentation and regulatory records.
- Develop and implement strategies for regulatory submissions that meet specific regional requirements.
- Ensure all regulatory procedures and documentation are prepared, reviewed, and submitted accurately and on time.
- Stay updated on changes in regulations and standards, and manage their impact on the company's practices.
- Coordinate with cross-functional teams to facilitate compliance with local and international standards.
- Conduct audits and reviews of regulatory procedures to enhance quality and compliance processes.
- Liaise with regulatory authorities and industry experts to maintain compliance and seek guidance as needed.
- Provide training and support to ensure staff are aware of regulatory requirements and company protocols.
- Manage regulatory documentation and maintain an organized system for instant retrieval and review.
- Preparation of registration dossiers as per regulatory guidelines.
- Preparation of renewal application as per renewal guidelines.
- Facilitate query response raised by regulatory authority and customers.
- Preparation and submission of Safety, Quality & administrative variations as per variation guidelines.
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