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
Senior Associate– API_RA
On-SiteGurgaon, Haryana, IN
On-Site • Gurgaon, Haryana, IN
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.
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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
Strong negotiation skills
Excellent oral and written communication skills with strong presentation skills
Significant knowledge of global, regional, national and other document development guidelines
Excellent computer skills; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)
Ability and desire to work in a team-oriented environment.
Excellent written and verbal communication skills
Highly proficient with Microsoft Word, PowerPoint and Excel.
Demonstrates ability to evaluate information and data with a defined, studied process and report results in a thoughtful, organized manner
Possesses a collaborative, results-driven style.
Flexible, Adaptive, Ability to work under pressure and provide quality outputs within tight timelines
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)
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