Regulatory Affairs Specialist

Regulatory affairs specialists play a vital role in ensuring compliance with regulatory requirements and facilitating the smooth operation of businesses.This position requires an individual with expertise in regulatory affairs, including experience with eCTD software and e-publishing requirements throughout the project lifecycle. The ideal candidate will...

Regulatory Affairs Manager Job DescriptionThe role involves developing and executing regulatory strategies, compiling and reviewing regulatory submissions, ensuring product compliance and acting as a key liaison with regulatory agencies.Key Responsibilities:Submission Management: Preparation, review and submission of regulatory documentation (e.g., dossiers,...

Job TitleRegulatory Executive - Product Compliance and Regulatory Affairs Specialist

As a qualified professional in the pharmaceutical industry, we are seeking an experienced individual to take on the role of Regulatory Affairs Specialist. The ideal candidate will have a strong understanding of various pharmacopoeias and regulations.The responsibilities of this position include:

Regulatory Affairs SpecialistThe role involves the compilation, submission and management of regulatory documentation for assigned projects.Responsibilities include maintaining accurate database records pertaining to products, in line with established systems and processes.Supporting and coordinating regulatory affairs projects, as assigned, including tender...

Regulatory Affairs ProfessionalJob Overview:We are seeking a highly skilled Regulatory Affairs Specialist to join our team. The successful candidate will be responsible for ensuring compliance with regulatory requirements for products, managing the submission process for regulatory approvals, and maintaining up-to-date knowledge of regulatory changes.Main...

Regulatory Affairs SpecialistJob Description:We are seeking a detail-oriented Regulatory Affairs Specialist to support end-to-end submissions for global markets. This role involves exposure to Lifecycle Management (LCM), Veeva Vault RIM, and complex Initial and Variation submissions.Key Responsibilities:Prepare Variation documents and/or evaluate...

Job DescriptionJob Description :Business: Piramal Critical CareDepartment: Regulatory AffairsLocation: KurlaTravel: LowJob OverviewThe Manager, Regulatory Affairs is responsible for the portfolio of Piramal Critical Care Products in the USA market. They will be responsible for authoring and reviewing submissions for dissemination to Health Authorities,...

Regulatory Affairs LeaderSr Manager Regulatory Affairs responsible for developing and executing regulatory strategies, compiling and reviewing regulatory submissions, ensuring product compliance, and acting as a key liaison with regulatory agencies.Key Responsibilities:Submission Management:Preparing, reviewing, and submitting regulatory documentation to...

Biologics Regulatory Affairs Job OverviewThis role involves strategic planning, execution and delivery of biologics clinical trials across EU and US markets. The ideal candidate will possess expertise in biosimilar clinical development, regulatory affairs, and eCTD submissions.About the RoleThe successful candidate will be responsible for developing and...