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

DDReg Pharma Pvt. Ltd.

Drug SafetyGMP ComplianceIPRLife SciencesPharmacovigilanceRegTechRegulatory AffairsRegulatory Intelligenceddregpharma.com

HQGurgaon, IN

Team Size88

Open Jobs12

Total Funding-

Latest FundraiseUnknown

Join the Team

Associate / senior Associate – API_RA

On-SiteGurgaon, Haryana, IN

On-Site • Gurgaon, Haryana, IN

Teeming tracks opportunities at over 24,000 AI startups, then works with you to find (and land) the one you'll love.

Frontend Developer

InternshipTel Aviv

Internship • Tel Aviv

Software Engineer

ContractCambridge, GB

Contract • Cambridge, GB

Machine Learning Engineer

InternshipManchester, GB

Internship • Manchester, GB

Mobile Developer

ContractNiš, RS

Contract • Niš, RS

Product Designer

InternshipMunich, DE

Internship • Munich, DE

AI Researcher

Full-timeUtrecht, NL

Full-time • Utrecht, NL

Job Descriptions

CMC review of technical documentation for regulatory filings to various markets – market: EU & UK, US- Gap Analysis and Remediation for module 3 -API
Prepare and compile Section 322, QOS & QbR ensuring that they are in conformance with applicable regulatory guidelines and that the highest quality standards are met.
Critically reviews documentation intended for submission to the respective agencies for internal consistency, for consistency to relevant guidelines and to promote regulatory excellence.
Demonstrate subject matter and area expertise.
Collaborate with internal and external clients,
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.

Education & Experience

Master’s degree in Pharma, Msc Chemistry
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4 to 6 years’) or equivalent combination of education, training, & experience.

Knowledge, Skills And Abilities

Excellent technical data interpretation skills
Excellent interpersonal skills including problem solving

Other Requirements As may be required from time to time – the incumbent may be required to working slots catering to different time zones

Location Gurgaon, Haryana (INDIA)

Related Blog Post