Regulatory Affairs Jobs in USA

OverviewFred Hutchinson Cancer Center is an independent nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.With a track...

Benefits:401(k) matchingFlexible scheduleHealth insuranceOpportunity for advancementPaid time offTraining & developmentBenefits/PerksCareers Advancement OpportunitiesFlexible SchedulingCompetitive CompensationBenefits including health insurance and 401(k).$40000 to $65000 depending on experience.Job...

DescriptionThis position is scheduled for 36 hours per week.This position is eligible for at $8000 sign on bonusSUMMARY:We are actively seeking passionate Speech-Language Pathologists (SLPs) to join our team in an in-person local traveling capacity. This position offers a dynamic work environment an...

Project Coordinator Tech OpsPosition Description SummaryThe Project Coordinator supports the execution of pharmaceutical projects across areas such as development manufacturing regulatory affairs or quality. This role ensures effective coordination of activities documentation and timelines while mai...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Company:At Annexon Biosciences we are a biopharmaceutical company advancing a late-stage clinical platform of novel therapies for people living with devastating classical complement-mediated neuroinflammatory diseases of the body brain and eye. Our novel scientific approach targets upstream C1q to b...

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together we support innovation from concept to commercialization offering expertise in regulatory strategy clinical tria...

What if the work you did every day could impact the lives of people you know Or all of humanityAt Illumina we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health t...

DescriptionAre you a quality-focused professional with a passion for ensuring product safety and compliance in the medical device industryWe are seeking a dynamic Sr. Recall Coordinator to oversee the preparation and execution of Field Actions for our Breast and Skeletal Health divisions. Based in N...

DescriptionAt CooperVision a division of CooperCompanies were driven by a unifying purpose to help people to experience lifes beautiful moments. We are connected through our shared values - dedicated innovative friendly partners and do the right thing. As a leading global manufacturer of contact len...

Coordinate all aspects of medication research and provide support to the Pharmacy Department and the clinical and research areas. Coordinate the Investigational Drug Service.Required Education and ExperienceGraduation from an accredited School of advanced pharmacy degree/residency or relevant lea...

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Companys Oncology medicines span all phases of clinical development (pre-clinical to post-licensure...

IntroductionWerfen Werfen is a growing family-owned innovative company founded in 1966 in Barcelona Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis Acute Care Diagnostics Transfusion Autoimmunity and Transplant. Through our Original Equipment Manufacturing (OEM...

DescriptionAre you passionate about driving innovation while ensuring compliance and quality in medical device development At Hologic we are seeking a Lead Design Assurance Engineer to play a pivotal role in new product development ensuring that design controls risk management and global regulatory...

Job Description About Allogene:Allogene Therapeutics with headquarters in South San Francisco is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management t...

Key ResponsibilitiesStrategic LeadershipLead the global medical strategy for Oncology brands across multiple indications within the tumour area.Ensure alignment between tumourlevel and brandlevel strategies to maximise medical impact.Serve as a core member of the Tumour Global Medical Senior Leaders...

Job DescriptionGeneral Summary:The Regulatory Labeling Senior Manager Rest of World (ROW) is responsible for development and maintenance of product labelling for ROW markets across all therapeutic areas. This includes prescribing and patient information and associated business processes.Key Duties a...

To be eligible for this position you must reside in the same country where the job is located.Associate Business Development Director Safety & Regulatory SolutionsLocation: US Greater Boston area NY/NJ VA/DC Metro CA areasThe Associate Business Development Director works collaboratively with other...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAbout the RoleWe are seeking a Manager to lead Product Operations team members within a regulated medical device environment. This onsite role in West Hills is focused on hands-on leadership execution excellence and close co...