Regulatory Affairs Specialist

Job Title: Regulatory Affairs SpecialistThis is a key role in our organization where you will be responsible for preparing, reviewing, and maintaining regulatory documents to ensure compliance with international guidelines and country-specific requirements.Key Responsibilities:Screen and analyze documents received for product registration requests as per...

Company DescriptionWe suggest you enter details here.Role DescriptionThis is a full-time on-site role for a Regulatory Affairs & Quality Assurance Officer. The role is located in Meerut. The Regulatory Affairs & Quality Assurance Officer will be responsible for ensuring compliance with regulatory requirements, overseeing quality control processes, conducting...

Company Description We suggest you enter details here. Role Description This is a full-time on-site role for a Regulatory Affairs & Quality Assurance Officer. The role is located in Meerut. The Regulatory Affairs & Quality Assurance Officer will be responsible for ensuring compliance with regulatory requirements, overseeing quality control processes,...

Company Description We suggest you enter details here. Role Description This is a full-time on-site role for a Regulatory Affairs & Quality Assurance Officer. The role is located in Meerut. The Regulatory Affairs & Quality Assurance Officer will be responsible for ensuring compliance with regulatory requirements, overseeing quality control processes,...

Regulatory Affairs OfficerJob Overview:We are seeking a skilled Regulatory Affairs Officer to oversee compliance with regulatory requirements and quality control processes.This is a critical role that requires strong analytical and communication skills, as well as the ability to work independently and collaboratively as part of a team.The successful...

Regulatory Affairs ProfessionalOverview:We seek a detail-oriented Regulatory Affairs Associate to support submissions for global markets. Required expertise includes Lifecycle Management (LCM), Veeva Vault RIM, and complex initial and variation submissions.Key Responsibilities:Prepare Variation documents and evaluate post-approval CMC changes in compliance...

Executive Quality Assurance Regulatory Affairs SpecialistThis role requires a strong understanding of quality systems and regulatory frameworks for medical devices. The ideal candidate will have hands-on experience with regulatory submissions, post-market surveillance, and risk management.The successful candidate will be responsible for ensuring compliance...

This is a full-time on-site role for a Regulatory Affairs & Quality Assurance Officer. The Regulatory Affairs & Quality Assurance Officer will be responsible for ensuring compliance with regulatory requirements, overseeing quality control processes, conducting quality audits, managing quality assurance processes, and developing and maintaining quality...

Job DescriptionThis role entails overseeing regulatory activities for FDA submissions, encompassing ANDA preparation, review, and filing. Key responsibilities involve managing CMC regulatory activities, coordinating compilation and submission of Annual Reports, and ensuring compliance with Batch Manufacturing Records.Key tasks include:Lead Regulatory...

Regulatory Affairs Specialist Role OverviewOur organization seeks a seasoned Regulatory Affairs professional with extensive expertise in pharmaceutical and medical device regulatory compliance.The ideal candidate will possess a deep understanding of international, federal, and local regulatory requirements across these industries.Key...