Executive - Regulatory Affairs

1 week ago

Bhiwadi RJ IN B. Braun Full time

You re an important part of our future Hopefully we re also a part of your future At B Braun we protect and improve the health of people worldwide You support this vision bringing expertise and sharing innovation efficiency and sustainability as values That s why we would like to keep developing our company with you Keeping your future in mind we re making a joint contribution to health care worldwide with trust transparency and appreciation That s Sharing Expertise Executive - Regulatory Affairs Company Ahlcon Parenterals IN Ltd Job Posting Location Bhiwadi R jasth n India Functional Area Regulatory Affairs Working Model Onsite Requisition ID 7394 JOB RESPONSIBILITIES - Total Experience Required Minimum 4 years in the Core Regulatory Affairs Department Qualification B Pharma M Pharma Minimum 3 years of experience in the compilation and preparation of dossiers for semi-regulated and regulated markets Analyze and respond to inquiries from regulatory agencies and customers worldwide ensuring timely submissions within set deadlines Maintain a well-organized and up-to-date regulatory filing system including databases and chronologies for easy tracking of changes made to documents submitted to agencies or partners Proactively update existing internal regulatory guidelines and develop new ones as needed to ensure alignment with current requirements Continuously stay informed about the latest regulations guidance documents and standards set forth by the FDA international regulatory bodies and domestic agencies relevant to the company s products Conduct thorough reviews of CMC Chemistry Manufacturing and Controls documents within established timelines To co-ordinate follow up for technical departments like R D QA QC ADL and Manufacturing for arranging the documents required for preparation compilation of Dossiers within defined timelines Managing the Registration Sample to deliver it to the customers within defined timelines Timely submission of dossier post approval submissions to the various Regulatory Authorities and the subsequent life cycle management To collect and compile the necessary documentation for the raw materials Active Pharmaceutical Ingredients API and excipients used in the manufactured batches intended for the registration of medicinal products in foreign countries Additionally to address and resolve any queries raised by government authorities during the registration reregistration process Take ownership of additional duties assigned to support the Regulatory Affairs department

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