Drug Development Regulatory Manager

Director, Disease BiologyAbout Septerna:We are a biotechnology company based in South San Francisco, CA. Our mission is to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company.Our Native Complex Platform recapitulates GPCRs with their native structure,...

Company OverviewA leader in oncology research and development, AbbVie is committed to discovering and delivering innovative treatments for various types of cancer. Our team works tirelessly to combine expertise in immuno-oncology, stem cells, and cell-signaling with knowledge of bispecific antibodies, antibody-drug conjugates (ADCs), and covalent-inhibitor...

Role OverviewWe are seeking a highly experienced Senior Immunology Research Scientist to join our team in the development of novel therapies for severe immune-mediated diseases related to glomerular kidney disease. As a key member of our late-stage drug development team, you will provide scientific leadership and expertise in the design, execution, and...

Pursue a Rewarding Career in Pharmaceutical Data ScienceWe are seeking an exceptional Clinical Data Insights Expert to join our Unreal Gigs team. As a critical member of our pharmaceutical data science department, you will work closely with clinical researchers, data scientists, and product development teams to analyze clinical, research, and market...

About Daiichi SankyoDedicated to creating innovative pharmaceutical therapies, Daiichi Sankyo Group has a legacy of over 110 years. With a presence in over 20 countries and a team of 16,000 employees worldwide, the company draws upon its rich history of innovation and a robust pipeline of promising new medicines to improve global healthcare standards.Our...

Job Summary">This is a pivotal role within EPM Scientific, responsible for overseeing operational activities related to drug safety studies from inception to completion. It involves monitoring clinical trial vendor activities and supporting key tasks related to case processing management in the Argus Safety Database, ensuring compliance with global clinical...

About Regulatory DataCorp, Inc.We are a leading provider of data risk management solutions for financial services and Fintech companies. Our mission is to keep criminal money out of the financial system by providing innovative solutions that help our clients stay ahead of emerging threats.The OpportunityWe are seeking an experienced Revenue Development...

Job OverviewAlumis Inc. is a pioneering precision medicines company dedicated to revolutionizing the lives of patients with autoimmune diseases. Despite significant advancements in treatment over the last two decades, many patients continue to suffer - our mission is to fundamentally change outcomes for these patients.We are seeking an exceptionally...

Drug Development ExpertiseWe advance science to improve lives.The Department of Safety Assessment at Genentech is seeking a highly skilled toxicologist to lead nonclinical studies and safety strategies in drug development. This position requires expertise in strategic planning and execution in toxicology.OpportunitiesThis project-facing role involves...

Job Summary:We are looking for a highly skilled Director of Regulatory Affairs and Compliance to oversee global regulatory activities and ensure seamless product approvals. The successful candidate will have a deep understanding of pharmaceutical regulations and practices, including FDA regulations and ICH guidance.This role involves leading interactions...

Gilead Sciences Inc. is a leader in the fight against diseases such as HIV, viral hepatitis, COVID-19 and cancer.We are seeking an experienced Medical Writer to join our team as Associate Director, Medical Writing.The successful candidate will be responsible for authoring a wide range of regulatory documents independently, including novel or atypical...

Job Description">We are seeking a Drug Development Data Scientist to join our team at Unreal Gigs. The ideal candidate will have a strong background in pharmaceutical data analysis, with experience working with clinical trial data and drug development processes.ResponsibilitiesAnalyze market data to assess the competitive landscape and forecast demand for...

We are seeking a seasoned expert in consumable development to drive our testing and validation efforts. This role will lead the qualification of consumables in compliance with ISO 10993, USP Class VI, and other regulatory standards.Key Responsibilities:Develop and execute comprehensive qualification plans for consumablesCollaborate with cross-functional...

Job Title: Regulatory Affairs Director for Pharmaceutical Product DevelopmentAbout Stirling Q&R:We are a leading pharmaceutical company in the San Francisco Bay Area, committed to developing and commercializing innovative therapeutic products. Our dynamic environment offers excellent opportunities for growth and professional development.Job Description:This...

Join Our Team as a Regulatory Compliance Engineer!Spirair, Inc. is a leader in the medical device industry, committed to delivering high-quality products that meet or exceed regulatory standards. As a Quality Engineer at Spirair, you will be responsible for supporting our Quality Management System, ensuring compliance with FDA regulations and industry...

About Daiichi Sankyo, Inc.">Daiichi Sankyo Group is a global pharmaceutical innovator dedicated to improving standards of care and addressing diverse unmet medical needs worldwide. With over 100 years of scientific expertise and a presence in more than 20 countries, the company has a robust pipeline of promising new medicines.">Our Vision">Under our 2025...

Job Description:We are looking for a highly skilled Regulatory Affairs Manager to join our team at Rigel Pharmaceuticals, Inc. As a key member of our regulatory affairs department, you will be responsible for providing regulatory expertise and policy support for good pharmaceutical development practices, contributing to the development of SOPs related to...

About Alumis Inc.Alumis Inc. is a precision medicines company driven by the mission to revolutionize patient outcomes in autoimmune diseases. Despite advances in treatment over the past two decades, many patients continue to suffer. Our goal is to fundamentally change these outcomes.We are seeking an exceptional individual to support global regulatory...

Job OverviewAbbVie is seeking a highly motivated and experienced Scientist I to join our Cell Culture Development Group in South San Francisco, CA. As a key member of our team, you will be responsible for developing and optimizing cell culture processes for GMP applications.Key ResponsibilitiesDesign and execute robust and scalable cell culture processes in...

At Alumis Inc., we are driven by a mission to transform the lives of patients with autoimmune diseases. With a focus on precision medicines, our goal is to fundamentally change outcomes for these patients.Job SummaryWe seek an exceptionally motivated individual to provide leadership and support to global regulatory activities, ensuring compliance with health...