DDReg Pharma

Job Type: Full Time

Associate/Sr Associate – QA

To provide Quality Assurance Support to DDReg’s Pharmacovigilance and Regulatory Services operations. Duties and responsibilities Quality assurance support and expert advice to operational Pharmacovigilance (PV) and Regulatory Services activities within DDReg in order to ensure compliance with applicable regulatory requirements and DDReg procedures and quality standards. Support maintenance of the Pharmacovigilance System Master File (PSMF) …

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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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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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Senior Medical Writer

To plan and Manage Medical Writing for Regulatory and Pharmacovigilance Verticals in compliance to applicable regulatory and Regulatory Guidelines. Duties and responsibilities Providing high-quality medical and scientific writing from planning and coordination of literature search through delivery of final drafts to internal and external clients. Prepare and review drug safety related documents including but not …

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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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Human Resources (Sr. HR) Manager

We are a leading pharmaceutical consulting firms, involved in a wide variety of pharma regulatory assignments from organizations across the globe for regulated and emerging markets. We are led by experts with a combined experience of ~80 years in handling global regulatory assignments & medical writing projects. DDReg supports large, medium and small size pharmaceutical …

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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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