DDReg Pharma is a global life sciences consulting firm specializing in regulatory affairs, pharmacovigilance, and quality services. With over 15 years of experience, they help pharmaceutical, biotech, medical device, veterinary, food supplement, and cosmetic companies navigate complex regulatory landscapes. DDReg offers solutions for IPR, GMP compliance, toxicology, and utilizes technology-driven tools like RIMS and an AI-driven Regulatory Intelligence platform to expedite product registrations and ensure compliance throughout the product lifecycle. Their business model is based on providing expert consulting services and technology-enabled solutions to accelerate revenue growth for life sciences companies.
Drug SafetyGMP ComplianceIPRLife SciencesPharmacovigilanceRegTechRegulatory AffairsRegulatory Intelligenceddregpharma.com
DDReg Pharma Pvt. Ltd.
DDReg Pharma is a global life sciences consulting firm specializing in regulatory affairs, pharmacovigilance, and quality services. With over 15 years of experience, they help pharmaceutical, biotech, medical device, veterinary, food supplement, and cosmetic companies navigate complex regulatory landscapes. DDReg offers solutions for IPR, GMP compliance, toxicology, and utilizes technology-driven tools like RIMS and an AI-driven Regulatory Intelligence platform to expedite product registrations and ensure compliance throughout the product lifecycle. Their business model is based on providing expert consulting services and technology-enabled solutions to accelerate revenue growth for life sciences companies.
Drug SafetyGMP ComplianceIPRLife SciencesPharmacovigilanceRegTechRegulatory AffairsRegulatory Intelligenceddregpharma.com
HQGurgaon, IN
Team Size88
Open Jobs27
Total Funding-
Latest FundraiseUnknown
Join the Team
Asst-Manager Drug Regulatory Affairs_ GHC/KSA_ (5+yrs Exp)
On-SiteGurgaon, Haryana, IN
On-Site • Gurgaon, Haryana, IN
Job Purpose
The Asst. Manager – Regulatory Affairs (GHC/KSA) will lead regulatory strategy, submissions, and compliance for pharmaceutical products intended for the ROW markets. This is an onsite role based in Gurgaon. The individual will serve as a key regulatory liaison, ensuring products meet all regulatory requirements, supporting lifecycle management, and facilitating timely approvals by the relevant authorities.
Key Responsibilities
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Data Scientist
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Product Designer
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Full-time • New York, US
Backend Developer
ContractUtrecht, NL
Contract • Utrecht, NL
Software Engineer
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Contract • Hamburg, DE
Frontend Developer
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Part-time • Munich, DE
Technical Writer
Part-timeNew York, US
Part-time • New York, US
Review of eCTD/CTD dossiers, variations, change controls, renewals and ensuring that they are in conformance with applicable regulatory guidelines and that the highest quality standards are met.
Tracking and responding to Authority queries within stipulated timelines; leading cross-functional action plans.
Critically reviews documentation intended for submission to the respective agencies for internal consistency, for consistency to relevant guidelines and to promote regulatory excellence.
Collaborate with internal and external clients via project trackers.
Demonstrate subject matter and area expertise.
Supporting and enabling effective and efficient communication that results in operational excellence.
Demonstrate high level knowledge of country regulations and regulatory guidelines as updated from time to time on various agencies’ website.
Educational Qualifications: B.Pharm / M.Pharm
Why Join Us
Opportunity to contribute to key regulatory submissions
Exposure to global health authority expectations
Skill development and continuous learning environment
Collaborative work culture
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