Regulatory Document Specialist
1 month ago
Overview:
We are seeking a highly skilled Regulatory Document Specialist to join our team at TransPerfect. As a key member of our team, you will play a vital role in ensuring the accuracy and compliance of regulatory documents.
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Regulatory Compliance Specialist
1 month ago
India Halma plc Full timeAbout Halma plc:Halma is a leading global life-saving technology group, driven by a clear purpose to improve safety and quality of life for people around the world.As an FTSE 100 company with headquarters in the UK and operations in over 20 countries, including regional hubs in India, China, Brazil, and the US, we offer a unique opportunity to work in a...
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Envu | Regulatory Affairs Specialist
1 day ago
india Envu Full timeWe're Hiring!Regulatory Affairs SpecialistAt Envu, we partner with our customers to design world-class, forward-thinking innovations that protect and enhance the health of environments around the world. We offer dedicated services in: Professional Pest Management, Forestry, Ornamentals, Golf, Industrial Vegetation Management, Lawn & Landscape, Mosquito...
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Medical Document Quality Assurance Specialist
4 weeks ago
India ARDEM Data Services Full timeARDEM Data Services is seeking a Medical Document Quality Assurance Specialist to join their team. As a key member of our organization, you will be responsible for ensuring the accuracy, quality, and compliance of medical documents with regulatory standards.The ideal candidate will have a strong educational background in life sciences or a related field,...
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Medical Documentation Specialist
4 weeks ago
India Immabeme Solutions Full timeWe are seeking a highly skilled Medical Documentation Specialist to join our team at Immabeme Solutions.The ideal candidate will have significant experience in ICU care and possess strong clinical documentation skills, including patient medical history and progress notes.The salary for this position is estimated to be around $120,000 - $180,000 per annum,...
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Senior Regulatory Affairs Specialist
4 weeks ago
India The Hird Full timeThe Hird is seeking a highly skilled Senior Regulatory Affairs Specialist to join our team in a remote location. This role offers a competitive salary of up to 19 LPA, with an estimated average annual compensation of 18.5 LPA.About the Role:We are looking for a seasoned professional with extensive experience in regulatory affairs and medical writing. As a...
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Senior Clinical Document Specialist
1 week ago
India Excelya Full timeAbout ExcelyaExcelya is a leading Contract Research Organization (CRO) in Europe, founded in 2014 and headquartered in Paris. Our global team consists of over 900 experts who understand the critical needs of our clients and provide innovative trial solutions across a broad spectrum of therapeutic areas.We take a collaborative approach to work, where shared...
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IQVIA | Regulatory Affair Specialist
1 day ago
india IQVIA Full timeJob Title / Primary Skill: Regulatory Affair Specialist Shift Timings : US EST timings (IST- 6.00 pm to 3.00 am) Job Location: Remote/Homebased Experience: 5 to 10 Years Job Overview: You will oversee all labelling activities for specified APIs and collaborates with our client and/or IQVIA stakeholders, such as Global Labeling, PV, GRLs and the LOCs (Local...
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Regulatory Publishing Specialist
1 month ago
India TransPerfect Full timeJob DescriptionAbout the Role:We are seeking a skilled eCTD Regulatory Document Professional to join our team at TransPerfect. As a key member of our regulatory publishing department, you will be responsible for preparing and submitting clinical study reports, IND documents, and NDA documents in accordance with ICH, eCTD, and other applicable electronic...
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India Straive Full timeCompany Overview:Straive is a pioneering technology firm committed to excellence in the field of chemicals regulations research.Job Description:We are seeking a highly skilled Regulatory Compliance Specialist to join our team. The ideal candidate will possess strong knowledge of chemicals regulations, particularly in the Middle East and Africa region.Key...
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Tag | Regulatory Specialist
2 days ago
india Tag Full timeREGULATORY SPECIALISTAt Tag, we help brands stand out and sell more by delivering impactful content, at speed and scale and across channels & geographies. With over fifty years of production experience for some of the world’s biggest brands, we partner with our clients to create work that is efficient, effective and more importantly tells a story.We...
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India Excelya Full timeEstablished in 2014 and headquartered in Paris, Excelya is a leading Contract Research Organization (CRO) with a global team of over 900 experts.We take a collaborative approach to work, ensuring our shared success through teamwork at every stage of a project. Our comprehensive services span regulatory affairs, clinical operations, quality assurance, and...
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Senior Regulatory Affairs Specialist
4 weeks ago
India Apsida Life Science Full timeApsida Life Science seeks an experienced Senior Regulatory Affairs Specialist to collaborate with our Global Regulatory Team Leads and submission teams. As a key member of our regulatory team, you will be responsible for ensuring timely and high-quality submissions that comply with global guidelines and company SOPs.The ideal candidate will have in-depth...
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Technical Documentation Specialist
1 day ago
India Scrut Automation Full timeAbout Scrut Automation: Scrut Automation is an information security and compliance monitoring platform designed for small and medium cloud-native enterprises. The company's mission is to empower businesses with a strong security posture and facilitate compliance with industry standards such as SOC 2, ISO 27001, and GDPR. With over 15 years of combined...
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Regulatory publisher ii
1 month ago
India TransPerfect Full timeOVERVIEW The Regulatory Publisher II is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, e CTD, and other applicable electronic publishing standards, as well as to prepare, assemble and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for...
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Senior regulatory publisher
1 month ago
India TransPerfect Full timeOVERVIEW The Senior Regulatory Publisher is responsible for working with Regulatory Affairs to publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, e CTD, and other applicable electronic publishing standards, as well as to prepare, assemble and submit applications (IND/CTA/NDA/MAA/NDA, etc.) for...
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Regulatory publisher ii
1 month ago
India TransPerfect Full timeDescription: Report directly to the Team Manager on all team and client issues, project work, project deliverables associated timelines, ensuring SLAs are satisfied, and deliver reporting – daily, weekly, or monthly Publish Clinical Study Reports, IND documents, NDA documents, and other regulatory documents according to ICH, e CTD, and other applicable...
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Packaging Technical Document Specialist
4 weeks ago
India TransPak Full timeJob SummaryWe are seeking a skilled Packaging Technical Document Specialist to join our team at TransPak. As a key member of our documentation team, you will be responsible for creating and maintaining technical documents related to packaging components and products.Key Responsibilities:Document Creation and Maintenance: Develop and maintain technical...
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Clinical Document Specialist II
10 hours ago
India TransPerfect Full timeAbout the role: As a Clinical Document Specialist II, you will be responsible for checking the quality of indexed documents in the eTMF and ensure they are filed correctly, with accurate metadata applied to each document. Occasionally, you may be assigned for more detailed eTMF quality review to ensure the eTMF is inspection ready. This role requires...
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Regulatory Content Specialist
5 days ago
India Straive Full timeJob OverviewThe Template Developer will be a key member of our team, responsible for supporting the development and delivery of regulatory content in machine-readable formats. This role requires a strong understanding of regulatory expectations and digital solutions.Key ResponsibilitiesDevelop WWI templates for regulatory documents, ensuring accuracy and...
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india raptorX.ai Full timeJob Title:Compliance and Regulatory SpecialistLocation:Hyderabad, IndiaExperience:6–10 yearsPosition Type:Full-TimeAbout RaptorXRaptorX leverages AI to empower financial institutions to detect, prevent, and comply with fraud and AML regulations globally. We’re hiring a Compliance and Regulatory Specialist to ensure RaptorX’s compliance in India, the...