DDReg Pharma

DELIVER BETTER DATA TO ENSURE FASTER APPROVAL

Full Time

Medical Writer – Associate/Sr Associate

To plan and Manage Medical Writing for Regulatory and Pharmacovigilance Verticals in compliance to applicable regulatory and Regulatory Guidelines Duties and responsibilities To plan and Manage Medical Writing for Regulatory and Pharmacovigilance Verticals in compliance to applicable regulatory and Regulatory Guidelines Providing technical consultation and provides substantive advice on strategy, regulations and industry best practices. …

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System Administrator

To plan and manage the information technology needs and systems, including implementing database and network designs, installing and upgrading software, ensuring systems security and troubleshooting computer issues. Duties and responsibilities Managing and maintaining the organization application and use of technology Manage window sever 2003 & 2012 (ADDS, DNS & DHCP) Assist & maintain corporate LAN/WAN …

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Content Writer

To develop and enrich content for DDReg tools, websites & Social media with new blog posts, guides and marketing copy.. Duties and responsibilities Develop content on regulatory affairs from related information available within company Research pharma industry-related topics (combining online sources, interviews and studies) Write clear marketing copy to promote our services Plan and develop …

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Content Strategist

DDReg company is looking to fill the role of content strategist. Please review the list of responsibilities and qualifications. While this is our ideal list, we will consider candidates that do not necessarily have all of the qualifications, but have sufficient experience and talent. Responsibilities for content strategist Utilize an understanding of target markets to …

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Senior Manager/Team Lead – Regulatory Affairs – Regulated Markets

To provide Regulatory Affairs support for EU in compliance to applicable regulations and guidelines. This position will provide support of the regulatory function through document management, electronic submission compilation and management, and other group management activities as required. Position will be required to work with Regulatory Affairs, Quality Assurance, Quality Control, Manufacturing, Research and Development …

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Associate/Sr. Associate – Regulatory Affairs (ROW)

Job purpose To carry out Regulatory Review and Compilation of Technical documentation & dossiers as part of Life Cycle Management of products in compliance to applicable regulations and guidelines. Education & Experience Master’s degree in Pharma discipline. 3 + years of experience in handling Regulatory Affairs function. Knowledge, Skills and Abilities Excellent technical data interpretation …

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React and Node Js Developer (MERN)

Skills And Requirements Full Stack developer, strong knowledge of JavaScript based framework having working experience in React JS. Develop and manage highly trafficked, highly scalable web properties with React.js and Next.js. Analyse, design, code, debug, test, document and deploy changes to the system. Troubleshooting interface software and debugging application codes. Understanding of RESTful APIs/GraphQL, HTML/CSS, …

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