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Job Description Regional Medical Advisor (RMA) - General & Specialty Medicine, South Region The RMA will serve as a key representative for…
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Our client, has been a pioneer in the manufacturing of nutritional healthcare products in India and has emerged as a multi product,…
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JOB DESCRIPTION:RESPONSIBLE FORExecute strategies developed for regulatory approvals as per annual registration plansTechnical Evaluation of the dossiers and files and compilation for…
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Location: Goa Job ID: 00012 Department: Business Development Responsibilities Assist in compiling, organizing, and maintaining product wise PMS data for inclusion in…
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Job Req ID: 45522 Location: Hyderabad, IN Function: Other About: Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership.…
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Job Description Regional Medical Advisor (RMA) - General & Specialty Medicine, East Region The RMA will serve as a key representative for…
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Job Description Regional Medical Advisor (RMA) - General & Specialty Medicine, North Region The RMA will serve as a key representative for…
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Job Title: Regulatory Documentation Candidate Fragrances & Aroma Ingredients Job Summary: We are seeking a highly motivated and experienced Regulatory Documentation Candidate…
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Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal…
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Director Power Utlity and Regulatory Practice 12+ Years Mumbai/Gurgaon Crescendo Global Mumbai, Maharashtra Jul 24, 2025We are hiring for an expert in Power Utility and Regulatory Affairs with a strong background in Infrastructure Advisory and Financial Due…
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Job DescriptionRegional Medical Advisor (RMA) General & Specialty Medicine, North RegionThe RMA will serve as a key representative for our company, engaging…
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Job Description: ? CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards. ? Draft, review, submission and…
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DRA Profile - Please find below the job description as requested. o Preparation of Dossier as per country guidelines (ACTD/CTD & Country…
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? Prepare, review, and submit DMFs/CTDs (USDMF, EDMF, CEP, etc.) for regulated and semi regulated markets ? Maintain regulatory documentation and lifecycle…
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Job Title: Technical Documentation Specialist - CE Compliance Department: Compliance / Regulatory Affairs / Engineering Location: Mohali Sector 82 Employment Type: Full…
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Regulatory Affairs Associate III, Labeling, Labeling Teva Pharmaceuticals Navi Mumbai, Maharashtra Jul 21, 2025Who we areTogether, we\'re on a mission to make good health more affordable and accessible, to help millions around the world enjoy…
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Regulatory Affairs Associate III, Labeling, Labeling Teva Pharmaceuticals Bangalore, Karnataka Jul 20, 2025
Who we are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world…
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Prepare, compile, and review CTD/eCTD dossiers for submissions (e.g., ANDA /NDA /MAA). Coordinate with cross functional teams (QA, QC, R&D, Manufacturing, Packaging)…
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Job Title: Regulatory Reporting ManagerCareer level DIntroduction to role:Are you ready to make a significant impact in the pharmaceutical industry? As a…
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The Position To Manage & execute the local RA activities according to ROPU RA strategies and local business priorities within the defined…
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