CMC Regulatory Affairs Specialist

Job Title: CMC Regulatory Affairs ManagerNet2Source Inc. is seeking a highly skilled CMC Regulatory Affairs Manager to join our team. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with regulatory requirements for our biologics products.Key Responsibilities:Prepare and submit high-quality CMC regulatory...

Job Title: CMC Regulatory Affairs ManagerNet2Source Inc. is seeking a highly skilled CMC Regulatory Affairs Manager to join our team.Job Summary:We are looking for a seasoned professional with extensive experience in CMC Regulatory Affairs to lead our team in preparing high-quality regulatory submissions for biologics products. The ideal candidate will have...

Job Title: CMC Regulatory Affairs Data Entry SpecialistFladger Associates is seeking a highly skilled Regulatory Affairs Data Entry Specialist to join our team in Foster City, CA. As a key member of our Regulatory Affairs team, you will be responsible for performing data entry using our Company RIM System to support key CMC RA stakeholders.Key...

Job Title: Senior Manager, CMC Regulatory Affairs, BiologicsJob Duration: 6 MonthsJob Location: Foster City, CAResponsibilities:Prepare Quality sections of INDs/IMPDs, new marketing authorization applications, post-approval variations, renewals, and responses to agency questions for biologics products.Interact with departments outside of CMC Regulatory...

About the Role:The Senior Director, CMC Regulatory Affairs for Biologics is responsible for leading a matrix team of professionals, who work with a specific product in Gilead's global portfolio of biological products in CMC Regulatory Affairs. This position will provide leadership at a product level as a global lead that ensures right first time global...

Job Title: CMC Regulatory Affairs Assistant II - Data EntryLeadStack Inc. is seeking a highly skilled and detail-oriented CMC Regulatory Affairs Assistant II - Data Entry to join our team. As a key member of our regulatory affairs team, you will be responsible for performing data entry using RIM System to enter relevant information to support key CMC RA...

Job Title: CMC Regulatory Affairs Assistant II - Data EntryWe are seeking a highly skilled and detail-oriented individual to join our team as a CMC Regulatory Affairs Assistant II - Data Entry. This is a remote opportunity with the possibility of working on-site in Foster City, CA.Key Responsibilities:Perform data entry using RIM System to enter relevant...

Job SummaryWe are seeking a highly skilled Senior Manager, Regulatory Affairs III to join our team at ATR International. This role will be responsible for leading the preparation of Quality sections of INDs/IMPDs, new marketing authorization applications, post-approval variations, renewals, and responses to agency questions for a range of biologics...

Job OverviewWe are seeking a highly skilled Senior Manager, Regulatory Affairs III to join our team at ATR International. This role will be responsible for leading the preparation of Quality sections of INDs/IMPDs, new marketing authorization applications, post-approval variations, renewals, and responses to agency questions for a range of biologics...

{"Responsibilities": "As a Senior Manager, Regulatory Affairs III at Gilead Sciences, you will be responsible for preparing high-quality regulatory submissions for biologics products. This includes preparing the Quality sections of INDs/IMPDs, new marketing authorization applications, post-approval variations, renewals, and responses to agency questions. You...

Regulatory Affairs Assistant - IIWe are seeking a highly skilled Regulatory Affairs Assistant - II to join our team at ATR International. This role is a great opportunity for someone who is passionate about advancing therapeutics against life-threatening diseases, while working with a collaborative team in Regulatory Affairs.Key Responsibilities:Perform data...

About the RoleWe are seeking a highly experienced and skilled Regulatory Affairs Director to lead our CMC Regulatory strategy for Adverum's gene therapy program/s. As a key member of our team, you will be responsible for developing, executing, and advising on global Regulatory CMC strategies through all phases of our development program/s.Key...

MFS Talent is seeking a highly skilled Regulatory Affairs Director to join our team. As a key member of our regulatory team, you will be responsible for providing strategic and operational regulatory input and support to collaboration with other project team members. Your expertise will contribute to the development of regulatory plans and strategies,...

About the RoleWe are seeking a highly experienced Regulatory Affairs Director to lead our CMC Regulatory strategy for our gene therapy programs. As a key member of our team, you will be responsible for developing, executing, and advising on global Regulatory CMC strategies across all phases of our development programs.Key ResponsibilitiesRegulatory Strategy...

Director of Regulatory AffairsHealthCare Recruiters International is seeking a seasoned Director of Regulatory Affairs to lead the regulatory function for a global leader in robotic systems for surgical interventions.Regulatory Leadership: Provide overall leadership of the regulatory function, interfacing with Clinical, Quality Assurance, and CMC...

Transformative Therapies for Autoimmune DiseasesNuvig Therapeutics is pioneering novel immune therapies to treat a broad spectrum of autoimmune diseases. Our treatments are designed to be active for a wide range of autoimmune diseases, without the inherent side effects and safety concerns of long-term treatment with existing therapies.Director, Regulatory...

Transformative Therapies for Autoimmune DiseasesNuvig Therapeutics is pioneering novel immune therapies to treat a broad spectrum of autoimmune diseases. Our treatments are designed to be active for a wide range of autoimmune diseases, without the inherent side effects and safety concerns of long-term treatment with existing therapies.Director, Regulatory...

**About the Role**HealthCare Recruiters International is seeking a highly qualified Director of Regulatory Affairs to join our team. As a key member of our R&D team, you will play a critical role in the development and commercialization of innovative robotic systems for the diagnosis and treatment of patients with advanced surgical interventions.**Key...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Director to join our team at Gilead Sciences, Inc. As a key member of our Global Regulatory Affairs organization, you will play a critical role in ensuring compliance with governing laws, regulations, and company policies while enabling the business to meet its goals and objectives.Key...

Transformative Therapies for Autoimmune DiseasesNuvig Therapeutics is pioneering novel immune therapies to treat a broad spectrum of autoimmune diseases. Our treatments are designed to be active for a wide range of autoimmune diseases, without the inherent side effects and safety concerns of long-term treatment with existing therapies.Director, Regulatory...