Regulatory Affairs Professional

About Cypress HCMCypress HCM is a leading company in the medical device industry, dedicated to providing innovative solutions for regulatory affairs and product development.

About Abbott LaboratoriesAbbott is a global healthcare leader committed to helping people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, encompassing diagnostics, medical devices, nutritionals, and branded generic medicines.We serve over 160 countries worldwide, with a diverse team of...

About the JobWe are seeking a highly skilled and experienced Regulatory Investigator to lead our investigative team in San Diego. As a key member of our Health Quality Investigation Unit, you will be responsible for overseeing complex investigations and ensuring that our department's regulatory requirements are met.Job SummaryThe successful candidate will...

Company OverviewThe clinical-stage biotech company, Dennis Partners, is a dynamic organization focused on developing innovative small molecule therapeutics for the treatment of devastating cancers and immune disorders. With multiple programs in clinical trials and a rapidly growing clinical portfolio, this is an exciting time to join our team as a Vice...

OverviewCrinetics Pharmaceuticals is a pioneering biotech company dedicated to developing innovative therapies for endocrine diseases and tumors. Our mission is to transform lives through rigorous innovation, patient-centric culture, and a team-oriented approach.We are seeking a highly skilled Manager, Regulatory Affairs to join our team in San Diego, CA....

Company Overview">Crinetics Pharmaceuticals is a pioneering pharmaceutical company dedicated to developing innovative therapies for endocrine diseases and tumors. Our team of experts is driven by a passion for science and a commitment to improving patient lives.">Salary Range">The anticipated base salary range for this role is $102,000-$136,000 per annum,...

About Us:Becton, Dickinson and Company is a leading global medical technology company that serves healthcare professionals and their patients in more than 190 countries.We are committed to advancing the world of health by developing innovative solutions that improve patient outcomes and enhance the quality of life for people around the world.Job Summary:The...

Job OverviewBioPhase Solutions is seeking a skilled Regulatory Affairs Specialist to join our team in San Diego, CA. As a key member of our organization, this role will focus on managing and maintaining documentation processes to ensure compliance with company policies and industry standards.ResponsibilitiesDocumentation Management: Coordinate the creation,...

About San Jose Water CompanySan Jose Water Company, a leading water utility in Silicon Valley, is seeking a highly skilled Regulatory Affairs Analyst to join our team. With over 150 years of experience, we pride ourselves on providing high-quality, life-sustaining water to over 1 million people.Compensation and BenefitsWe offer a competitive annual salary of...

Job SummaryWe are seeking a highly skilled Regulatory Affairs CMC Associate to join our team at Fladger Assoc. Inc. in Foster City, CA. This is an exciting opportunity for a professional with a strong background in regulatory affairs and experience in supporting biologic and small molecule drugs.About the RoleThe successful candidate will provide regulatory...

Key Responsibilities:As a Regulatory Affairs Expert at Daiichi Sankyo, you will play a critical role in ensuring the compliance of our products with global regulations and guidelines. This includes managing the development and maintenance of Company Core Data Sheets (CCDS) for assigned products, as well as driving the maintenance of global labeling and...

About Daiichi SankyoDaiichi Sankyo Group is a pharmaceutical leader with over 125 years of scientific expertise and a presence in more than 20 countries. We are dedicated to creating innovative therapies that improve standards of care for patients globally.Our company's vision is to become a global pharma innovator with a competitive advantage in oncology,...

Fladger Assoc. Inc. is seeking a highly skilled Regulatory Affairs CMC Associate to join our team in Foster City, CA.About the RoleThis exciting opportunity offers a competitive salary of approximately $120,000 - $180,000 per year, commensurate with experience, plus benefits.Key ResponsibilitiesProvide Regulatory CMC support for biologic and small molecule...

Job OverviewFoster City, CA - Fladger Assoc. Inc.About the RoleThis Regulatory Affairs Associate position is an excellent opportunity for a detail-oriented professional to join our team in Foster City, CA. The successful candidate will have experience with regulatory compliance and be able to work under deadlines.ResponsibilitiesPrepare Drug Listings/Lot...

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...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Supervisor to join our team at AppleOne. This is a unique opportunity to work with a leading workforce management company that is committed to excellence in Human Resources and Strategic, Inclusive Procurement.

About Daiichi Sankyo, Inc.Daiichi Sankyo Group is a leading pharmaceutical company with a rich legacy of innovation spanning over 125 years. With a presence in more than 20 countries and a team of approximately 18,000 employees worldwide, we are committed to delivering innovative therapies that address unmet medical needs globally.Salary: $120,000 - $180,000...

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...

Cypress HCM seeks a skilled Regulatory Affairs Specialist to coordinate the accumulation of technical information and prepare submissions for in vitro diagnostic and medical device licenses to various governmental regulatory agencies. This role involves coordinating clinical study trials, including offsite locations as needed.Key ResponsibilitiesSubmission...

About Daiichi Sankyo, Inc.Daiichi Sankyo Group is a pharmaceutical company dedicated to creating and supplying innovative therapies to improve healthcare standards globally. With over 100 years of scientific expertise and a presence in more than 20 countries, the company leverages its world-class science and technology to address diversified, unmet medical...