Regulatory Affairs Specialist

Job Title: CMC Regulatory Affairs Data Entry SpecialistRICEFW Technologies is seeking a highly skilled and detail-oriented CMC Regulatory Affairs Data Entry Specialist to join our team. As a key member of our Regulatory Affairs department, you will be responsible for performing data entry using Gilead RIM System to support key CMC RA stakeholders.Key...

Job Summary:The Principal Regulatory Specialist will play a key role in ensuring the overall regulatory compliance of Presidio Medical, Inc. with applicable regulatory bodies and the Presidio Quality Management System (QMS). This position will work closely with the Regulatory Affairs department to evaluate design control projects, document change orders, and...

Job Title: Regulatory Affairs Assistant - IIJob Summary:We are seeking a highly skilled Regulatory Affairs Assistant - II to join our team at Collabera. As a key member of our Regulatory Affairs team, you will be responsible for performing data entry, RIM System, and ensuring the completeness, correctness, and consistency of data.Key Responsibilities:Perform...

Job OverviewFladger Assoc. Inc. is seeking a highly skilled Regulatory Affairs Associate to join our team in Foster City, CA. This is a contract position with a duration of 12-18 months and a negotiable rate.Key Responsibilities:Prepare Drug Listings/Lot Distribution Reports (Biologics) and compile documentation for Certificate of Pharmaceutical Product...

Job OverviewUnicon Pharma Inc is seeking a highly skilled Regulatory Affairs Assistant to join our team. As a key member of our Regulatory Affairs department, you will play a crucial role in ensuring the accuracy and completeness of data entry in our RIM System.Key Responsibilities:Perform data entry tasks using our RIM System to support key CMC RA...

Job SummaryThe Principal Regulatory Specialist will play a key role in ensuring the overall regulatory compliance of Presidio Medical, Inc. with applicable regulatory bodies and the Presidio Quality Management System (QMS). This position is responsible for participating in design control projects, evaluating document change orders for regulatory assessment,...

Senior Regulatory Affairs SpecialistWe are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team at ACON Laboratories. As a key member of our regulatory affairs team, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements.Key Responsibilities:Coordinate the preparation and...

Job Title: Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Tandem Diabetes Care. As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements for our medical devices.Key Responsibilities:Prepare and maintain domestic and international regulatory...

Job Title: CMC Regulatory Affairs, Data Entry ContractorA leading pharmaceutical company is seeking a highly skilled CMC Regulatory Affairs, Data Entry Contractor to join their team in Foster City, CA. This is a 6-month contract with a possible extension.Job Summary:The successful candidate will be responsible for performing data entry using the Company's...

Senior Regulatory Affairs Specialist **About the Role** We are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team at ACON Laboratories. As a key member of our regulatory affairs team, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements. **Key Responsibilities** *...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Tandem Diabetes Care. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and guidelines for our medical devices.Key ResponsibilitiesPrepare and maintain domestic and international regulatory filings...

Senior Regulatory Affairs SpecialistAt ACON Laboratories, we are committed to developing innovative medical devices that enhance human life. We are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team.The ideal candidate will have a strong background in medical devices regulations and terminologies, with a minimum of 6-7 years of...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Tandem Diabetes Care. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and guidelines for our medical devices.Key ResponsibilitiesPrepare and maintain domestic and international regulatory filings...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Tandem Diabetes Care. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and guidelines for our medical devices.Key ResponsibilitiesPrepare and maintain domestic and international regulatory filings...

Regulatory Affairs Specialist Job DescriptionYoh is seeking a highly skilled Regulatory Affairs Specialist to join our team in St. Louis, Missouri. This individual will be responsible for planning and authoring pharmaceutical documents, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams.Key Responsibilities:Plan...

Job Title: Regulatory Specialist, R&DBayside Solutions, Inc. is seeking a highly skilled Regulatory Specialist to join our R&D team. As a Regulatory Specialist, you will play a critical role in implementing worldwide regulatory programs for developing and marketed products and interacting with regulatory authorities to expedite approvals.Key...

Join Abbott Laboratories as a Regulatory Affairs Specialist IIAt Abbott Laboratories, we are committed to helping people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines.We are...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Tandem Diabetes Care. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and guidelines for our medical devices.Key ResponsibilitiesPrepare and maintain domestic and international regulatory filings...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Tandem Diabetes Care. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and guidelines for our medical devices.Key ResponsibilitiesPrepare and maintain domestic and international regulatory filings...

Job DescriptionGilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops, and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world.Director, CMC Regulatory...