DDReg Pharma

Job Location: Mumbai

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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