Expert Regulatory Affairs Professional

Role - Regulatory Affairs - Medical Devices Experience - 1 to 3 Years Location- Madhavaram Chennai Budget - As per the industry Key Responsibilities 1 Regulatory Submissions Prepare and submit regulatory documents to authorities for approval such as new product applications amendments and supplements 2 Compliance Ensure products meet...

Regulatory Affairs Specialist Job OpportunityThe ideal candidate for this position will have a strong background in regulatory affairs, with a focus on CMC and USFDA submissions.A key responsibility of the role is leading and managing CMC regulatory activities, including preparing and reviewing technical documents such as Module 2 & 3 (CTD format).Key...

JOB DETAILS Candidates should review and prepare regulatory submissions, including new ANDA filings, amendments and Annual reports to the ANDA.Review of DMF Manages USFDA registration activities FUNCTIONAL AREA Pharma Jobs Consultancy in Chennai, Pharma Jobs Consultancy near me, Pharma Jobs, Top, Best, Jobs Consultancy in Chennai, regulatory affairs jobs...

Job Description- Prepare, review, and submit amendments and supplements for the assigned products.- Prepare summary documents for regulatory submission.- Prepare, review, and submit responses to the Agency s queries for the assigned products.- Compile and submit Global Annual Reports.- Review stability protocols and reports, analytical method validation...

Job DescriptionDescriptionRegulator ChemistLocation: Chennai, IndiaRequired Language: EnglishEmployment Type: Full-TimeSeniority Level: AssociateTravel Mode: ModerateAbout UsBuckman is a privately held, global specialty chemical company with headquarters in Memphis, TN, USA, committed to safeguarding the environment, maintaining safety in the workplace, and...

Regulatory Compliance ExpertAbout the Role:We seek a highly skilled Regulatory Compliance Expert to ensure adherence to regulatory requirements and implement effective quality management systems.Main Responsibilities:Document Control: Prepare and review QMS-related documents, including SOPs, work instructions, and templates for validation, qualification, and...

Job TitleSenior Business Analyst with HealthCareJob DescriptionGather, analyze and document business requirements related to regulatory compliance and payer guidelines. Ensure system changes, processes and documentation remain compliant with regulations.Key Responsibilities:Regulatory ComplianceBusiness Requirements AnalysisSystem Change...

Medical Affairs Specialist - India Chennai Trivandrum - Office or Home BasedICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence and we welcome you to join us on our mission to shape the future of clinical developmentOverview Provide support...

Use Your Power for PurposeWe're committed to delivering medicines to the world with greater speed, without compromising on excellence and integrity. Navigating both local and global regulations is crucial, and the dynamic regulatory landscape demands innovative thinking and meticulous attention to detail. Your role will be instrumental in ensuring that our...

Job OpportunityWe seek a skilled Regulatory Chemist to perform critical tasks in product regulatory approval.Purpose and ResponsibilitiesPrepare and submit regulatory documents for compliance review.Develop strategies to meet evolving regulatory demands.Coordinate product registration with provincial guidelines and third-party suppliers.RequirementsTo...