Regulatory Affairs Jobs in Mumbai

Piramal Pharma Limited - Mumbai, India

for Raw material, Intermediates, and Drug substance and equipment cleaning. Method validation for related substances, assay and carryover study. Support to regulatory affairs and customers for queries Not Mentioned

from: Monsterindia.com - More than 30 days ago

Kimberly-Clark Lever Limited - Mumbai, India

local and global regulatory affairs. Supports regulatory information management system governance processes and regulatory data management (systems, tools, documents, records, and standards). Support Not Mentioned

from: Monsterindia.com - More than 30 days ago

Piramal Pharma Limited - Mumbai, India

entry, peer review and submission to applicable regulatory authorities within stipulated timelines Key Stakeholders: Internal Quality Sales Supply Chain and Regulatory Affairs teams Experience: Overall, 2 Not Mentioned

from: Monsterindia.com - More than 30 days ago

Abbott Vascular - Mumbai, India

of Experience: at least 7 years in Regulatory Affairs & RA compliance, data analysis, project Management u2026 Language: Fluent English Location:India Mumbai Not Mentioned

from: Monsterindia.com - 4 days ago

Sanofi - Mumbai, India

and proactively engage with HAs Conduct regulatory due diligence for business collaborations Experience: About 3-5 experience in Regulatory Affairs including managing India and South Asia market. Good understanding Not Mentioned

from: Monsterindia.com - More than 30 days ago

Sanofi - Mumbai, India

trackers and global databases. About you Experience: About 3-5 experience in Regulatory Affairs including managing India and South Asia market. Good understanding of the consumer healthcare Not Mentioned

from: Monsterindia.com - More than 30 days ago

Sanofi - Mumbai, India

in accordance with local regulations Ensure that coordinated contact is maintained with other functions within Sanofi namely Purchasing, Legal, Supply Chain, Drug Regulatory Affairs, and Marketing etc for timely Not Mentioned

from: Monsterindia.com - More than 30 days ago

Novartis India - Mumbai, India

of Informed Consent Forms, engaging Regulatory Affairs/CTA Hub for Health Authorities submissions, as required Prepares and finalizes local submission package for submission to IRB/IEC, CTA Hub (Europe: acc Not Mentioned

from: Monsterindia.com - More than 30 days ago

EYEGLOBAL SOLUTIONS PVT. LTD. - Thane, India

) guidelines. Qualifications and Experience: MBBS, MD, or Pharmacology degree from a recognized institution 1. 15+ years of experience in clinical research and regulatory affairs within the pharmaceutical Not Mentioned

from: Monsterindia.com - 20 days ago