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Drug Regulatory Affairs Openings | Corpseed
Overview
Position Name: Regulatory Affairs
Organization: Corpseed
Qualification: B.Pharm, M.Pharm, Msc, BSc, Ph.D
Experience: 1 to 2 Years
Salary: Not disclosed
Location: Noida
About Us: Corpseed is a prominent player in the compliance and regulatory affairs sector, specializing in various regulatory requirements for medical devices, drugs, and cosmetics. Based in Noida, Uttar Pradesh, Corpseed provides comprehensive services including CDSCO registration, quality certification, and compliance with multiple regulatory standards. The company is dedicated to helping businesses navigate complex regulatory environments and ensuring adherence to industry standards.
Job Responsibilities
- Handle CDSCO registration for medical devices, drugs, and cosmetics, ensuring compliance with relevant rules and standards.
- Draft, review, and submit regulatory documents and maintain archival records for the Indian market.
- Utilize government websites for application filing and review technical documents before submission on the CDSCO portal.
- Ensure compliance with Medical Device Rules 2017, ISO standards, BIS registration, ISI/FMCS registration, BEE registration, WPC approval, FDA registration, Legal Metrology registration, Pollution NOC, and waste management compliance.
- Address and manage technical queries related to CDSCO registration and client needs.
- Work on documentation for quality certifications and designing testing machines as per Indian standards.
How to Apply
Interested candidates should send their resumes to nitisha.kumari@corpseed.com.
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