Job Purpose : Provide expert advice and support to labelling stakeholders with respect to global and local Product Information (PI) processes. Timely…
Coordinate and prepare technical files for submission to regulatory bodies with appropriate input from supporting functions (R&D, Quality, Manufacturing, Medical Affairs, etc.).
\ \ Role: R&D Regulatory InternWho Can Apply: LGBT+ Job Seekers Only (B.Pharm/M.Pharm Graduates Only)Location: BengaluruQualification B.Pharm / M.Pharm (2022, 2023 &…
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Job Description: ? CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards. ? Draft, review, submission and…
### Job Description We are currently seeking an Assistant Manager - Medical and Scientific Affairs to join our growing team. Within the…
Department: RA CMC & DeviceAre you passionate about your work? Do you want to build excellence within processes in the most efficient…
Job Description: ? CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards. ? Draft, review, submission and…
Department : Regulatory Affairs Designation : Officer/Executive R.A Officer/Executive in a Gummies Manufacturing Company would play a crucial role in ensuring that…
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.Department: Regulatory Affairs Rare Blood DisordersAre you passionate about driving regulatory strategy and life cycle management of product portfolio ensuring interactions with…
Manager Quality Assurance * Location: Mumbai Job type: Permanent About the jobAt Sanofi Consumer Healthcare, we have one overarching mission to work…
Why Patients Need YouWe\'re looking to bring medicines to the world faster and we are not willing to compromise on excellence and…
\ \ The Associate Director/Director (Global Regulatory Leader), Global Regulatory Affairs (GRA), Specialty Business (Brands and Innovative Medicines), partners with leaders across…
\ \ Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India\\\'s leading telecom service provider. The…
This is where you save and sustain livesAt Baxter, we are deeply connected by our mission. No matter your role at Baxter,…
\ Job description:Roles and Responsibilities: Ensure timely authoring and submission of dossiers (Module 2 5) for regulated and ROW in the eCTD…
DMF API Submission experience is must Preparation of New Drug Master Files as well as DMF amendments for Brazil, US, and ROW…
Department : Regulatory Affairs Industry Type Cosmetic Position : R&D Responsibilities : ? Review formulations and claims and provide regulatory guidance to…
Regulatory affairs 4+ years of experience agrochemical/pesticide. Experience with regulatory submissions, dossier preparation, and interactions with regulatory authorities. Ellora park vadodara Job…