BLA Regulatory Publishing Specialist – Veeva eCTD

Job OverviewThe Regulatory Publishing Specialist will be responsible for managing and preparing regulatory submissions in electronic format using Veeva Vault eCTD Publishing.Key Responsibilities:Compile, format, and publish regulatory documents according to global health authority requirements.Ensure compliance with regulatory guidelines (FDA, EMA) and...

Job Summary:This is a high-level technical role focusing on delivering exceptional customer experiences through expert Veeva CRM support. Key Responsibilities include:Providing advanced technical assistance for Veeva CRM applicationsTroubleshooting complex technical issues efficiently and effectivelyCollaborating with cross-functional teams to resolve...

Desktop Publishing SpecialistWe are seeking a skilled Desktop Publishing Specialist to join our team.The ideal candidate will have good skills in Adobe InDesign, Illustrator, Photoshop, Ms-Word and PowerPoint.Experience in Localization industry/projects is highly preferred. This includes working on different languages in InDesign, MS Word, OCR Tasks, and...

Job Title: Regulatory Compliance SpecialistThis role requires an individual with strong regulatory knowledge to ensure compliance with industry standards and regulations.">Key Responsibilities:Regularly review and update compliance processes to ensure alignment with changing regulations.Coordinate with stakeholders to maintain awareness of regulatory...

Job Title: Regulatory Compliance SpecialistKey Responsibilities:Ensure strict adherence to RBI and SEBI regulations.Assess the impact of regulatory changes on business processes and policies.Disseminate updates to senior management and ensure timely implementation.Develop and implement the annual compliance testing plan.Report significant compliance lapses...

Job Title: Regulatory Compliance SpecialistOverview:As a key member of our team, you will ensure that we maintain the highest standards of regulatory compliance. Your expertise in statutory and regulatory requirements, as well as internal governance frameworks, will be crucial in identifying and mitigating risks.Key Responsibilities Include:Conducting...

Job Title: Scientific Content SpecialistOur organization seeks an experienced Medical Writer to develop high-quality, regulatory-compliant content for the pharmaceutical sector. The ideal candidate will possess a strong background in medical writing/scientific communications and be proficient in publication and regulatory writing.Key...

Regulatory Affairs SpecialistThe ideal candidate will be responsible for leading and managing CMC regulatory activities, including USFDA submissions.Key Responsibilities:Compile and submit Annual Reports, amendments, and deficiency responses to ensure compliance with regulatory requirements.Interface with cross-functional teams to gather required...

Product Support AssociateWe are seeking a highly skilled Product Support Associate to join our team. The ideal candidate will have excellent communication skills, a customer-first mindset, and the ability to work in a fast-paced environment.This role involves providing exceptional support to authors through various channels, including email and phone calls....

Regulatory Intelligence SpecialistAbout Our OrganizationWe are a forward-thinking company focused on leveraging our comprehensive dataset to drive business success in the life sciences sector.Our MissionWe help companies navigate complex regulatory landscapes by providing timely and accurate regulatory intelligence insights.ResponsibilitiesParticipate in...