Regulatory Affairs Jobs in Kanpur
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Search Results - Regulatory Affairs Jobs in Kanpur
vueverse.-Kanpur
Senior Regulatory Affairs Specialist
Experience: 6–8 Years
Domain: Medical Devices / Combination Products
Role Overview
We are looking for an experienced Regulatory Affairs Specialist with strong expertise in combination products and medical...
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Sharvam compliance-Kanpur
QA teams trying to close out regulatory findings before a re
• inspection.
You understand what it costs
• operationally, commercially, and reputationally
• when a site's response is inadequate.
You have relationships. With QA Heads, Regulatory Affairs...
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Mashreq-Kanpur
Role Overview:
This is a senior leadership role within the Corporate Affairs Group, forming part of the Head Office IBG Finance Team. The role supports Mashreq’s strategic finance agenda through close partnership with IBG leadership and alignment...
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Republic World-Kanpur
Job Title: Senior Legal Manager
Department: Legal & Regulatory Affairs
Location: Republic Media Network, Noida
Experience: 8-10 Years
Employment Type: Full-Time
About Republic Media Network
Republic Media Network is a leading Indian news...
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ENGIE India-Kanpur
Tamil Nadu
Location: Pune / Noida
Department: Project Development
Reporting To: Head – Corporate Affairs, Land & ESG India / MD India
Key Responsibilities
1. Project Development & Deal Execution
• Contribute to renewable growth objectives for ENGIE...
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Mashreq-Kanpur
Role Overview:
This is a senior leadership role within the Corporate Affairs Group, forming part of the Head Office IBG Finance Team. The role supports Mashreq's strategic finance agenda through close partnership with IBG leadership and alignment...
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ProPharma-Kanpur
the deliverable timelines.
• Interacts and collaborates with subject matter experts in clinical operations, data management, biostatistics, regulatory affairs, etc., as needed, to produce writing deliverables.
• Coordinates QC reviews of documents and maintains...
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Sharvam compliance-Mumbai, 1123 km from Kanpur
regulatory findings before a re-inspection. You understand what it costs — operationally, commercially, and reputationally — when a site's response is inadequate.You have relationships. With QA Heads, Regulatory Affairs Directors, Site Quality Heads, Plant...
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ProPharma-Kanpur
the deliverable timelines.
• Interacts and collaborates with subject matter experts in clinical operations, data management, biostatistics, regulatory affairs, etc., as needed, to produce writing deliverables.
• Coordinates QC reviews of documents and maintains...
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MasterControl-Kanpur
new levels of operational excellence across product development, clinical trials, regulatory affairs, quality management, supply chain, manufacturing and postmarket surveillance. For more information, visit www.mastercontrol.com.
SUMMARY
The Customer...
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