Regulatory Affairs Jobs in Chennai
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Search Results - Regulatory Affairs Jobs in Chennai
vueverse.-Chennai-
R&D, Quality, Clinical, and Manufacturing.
• Monitor regulatory changes and assess impact on ongoing projects.
Requirements:
• 8+ years of experience in medical device regulatory affairs.
• Bachelor's degree or higher in Biomedical Engineering, Life...
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WinnerBrands-Chennai-
Powered by AI-driven optimization, it enables more sustainable, transparent supply chains.
Role Overview:
The Public Affairs Consultant will play a critical role in shaping and executing the organization's government affairs and public policy strategy...
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P360-Chennai-
regulatory data harmonization and governance
• Collaborate with Regulatory Affairs, IT, and external partners
• Support inspections, audits, and health authority submissions
• Provide functional leadership across multiple RIM workstreams
Required...
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WinnerBrands-India-
Powered by AI-driven optimization, it enables more sustainable, transparent supply chains.
Role Overview:
The Public Affairs Consultant will play a critical role in shaping and executing the organization's government affairs and public policy strategy...
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vueverse.-Chennai-
/ Statistical Programmers
Clinical Research professionals
Pharmacovigilance specialists
Regulatory Affairs professionals
HEOR / Market Access specialists
Bioinformatics / Data Science roles
Conduct initial screening interviews to assess technical fit...
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WinnerBrands-Chennai-
Powered by AI-driven optimization, it enables more sustainable, transparent supply chains.
Role Overview:
The Public Affairs Consultant will play a critical role in shaping and executing the organization's government affairs and public policy strategy...
Read more
Medaffin-Chennai-
Dentists
Medical Affairs & Regulatory Professionals
Pharmacovigilance Specialists
Clinical Research Associates
Recently retired or part-time practitioners are equally welcome
Minimum Requirements
Professional degree or license in a clinical field (MBBS, MD...
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Rose International-Chennai-
clinical research, healthcare, and life sciences roles (e.g., Clinical Research Associates, Clinical Data Managers, Regulatory Affairs Specialists, Clinical Trial Assistants, Pharmacovigilance Associates, etc.).
• Use niche clinical sourcing platforms...
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Medaffin-India-
Physiotherapists & Allied Health · Dentists
Medical Affairs & Regulatory Professionals
Pharmacovigilance Specialists
Clinical Research Associates
Recently retired or part-time practitioners are equally welcome
Minimum Requirements
• Professional degree...
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Cytel-Chennai-
Development, Data Management, Biostatistics, Regulatory Affairs, and IT to align digital strategy.
• Represent the organization in industry working groups or standards forums as appropriate.
• Provide training and knowledge-sharing sessions on USDM and Digital...
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Freyr Solutions-Chennai-
Regulatory affairs knowledge or background is a bonus.Proven track record in sales and achieving quarterly and yearly targets.Go-getter and self-motivated. Must be able to perform without constant managerial intervention.Prior experience in cross-functional...
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ProPharma-Delhi, 1759 km from Chennai-
meetings (e.g., project kickoff, comment review), and manages the deliverable timelines.Interacts and collaborates with subject matter experts in clinical operations, data management, biostatistics, regulatory affairs, etc., as needed, to produce writing...
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Standard Chartered-Chennai-foundit.in-
for a given Strategy and Talent project (Includes functions such as HR, Corporate Affairs & Brand & Marketing (CABM), Supply Change Management (SCM) and Property)). This role entails crafting comprehensive change management strategies, fostering seamless...
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e-Hireo Global Solutions-Chennai-updazz.com-
market trends, and emerging fintech innovations
• Stay updated on current affairs and regulatory developments in the Indian BFSI sector
Key Requirements
Experience : 3+ years of enterprise sales experience in a fintech or SaaS company
Industry...
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IQVIA-Chennai-
expertise in International Pricing & Market Access (PMA), with desirable additional experience in forecasting, clinical development, regulatory affairs, access, or medical writing.
• Strong project management, client‑facing skills, and the ability...
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