Regulatory Affairs Lead Jobs in USA

The Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years...

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...

Job Title -Regulatory Affairs Professional 4 Duration: 12 months-possible to extend Location Newton MA 02466 Shift : 1st Pay rate-on basis of exp-negotiable Description: As a Regulatory Affairs Specialist Consultant you will be responsible for: Formulate and execute activities associated...

Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide The opportunity below is with one of our clients a leading global medical technology company. This organization provides a wide rang...

Position SummaryAs the Director of Regulatory Affairs and Quality Assurance (RA/QA) this position is responsible for ensuring global leadership in RxFunction by influencing the creation of and ensuring compliance with the global regulatory requirements for the companys emerging medical device initia...

The Sr. Regulatory Affairs Specialist is responsible for creating and assuring compliance of federally regulated product label information including nutrition ingredient declaration allergens claims and associated product communication. This position manages several projects while working cross-func...

At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 associates we innovate fearlessly champion progress and act swiftly to impact global eye health. We foster an inclusive culture recognizing your contributions and offering opportunities to grow yo...

Working TitleNAGPRA & Tribal Affairs LeadSF StateUniversitySan Francisco State is an Equal Opportunity Employer and does not discriminate against persons on the basis of race religion color ancestry age disability genetic information gender gender identity gender expression marital status medical co...

Working TitleNAGPRA & Tribal Affairs LeadSF StateUniversitySan Francisco State is an Equal Opportunity Employer and does not discriminate against persons on the basis of race religion color ancestry age disability genetic information gender gender identity gender expression marital status medical co...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSummarized PurposeThe Global Labeling & Lifecycle Document Specialist (GL&LDS) Team is responsible for managing global labeling activities and ensuring compliance with international regulatory standards. This role coordinate...

We are seeking early to midcareer professionals to support global regulatory and ethics & compliance activities for our clients in the life sciences industry.Key Responsibilities:Support regulatory strategy for new products and changes (devices drugs combination products digital health/SaMD).Help pr...

Working TitleNAGPRA & Tribal Affairs LeadSF StateUniversitySan Francisco State is an Equal Opportunity Employer and does not discriminate against persons on the basis of race religion color ancestry age disability genetic information gender gender identity gender expression marital status medical co...

Working TitleNAGPRA & Tribal Affairs LeadSF StateUniversitySan Francisco State is an Equal Opportunity Employer and does not discriminate against persons on the basis of race religion color ancestry age disability genetic information gender gender identity gender expression marital status medical co...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Job Description SummaryThis position provides regulatory strategy and direction to the Premium Segment of the Magnetic Resonance Imaging business regarding healthcare industry regulatory requirements for product launch premarket submissions/registrations and postmarket compliance working closely wit...

Job DescriptionAssociate Director Regulatory Submissions Archive OperationsLocation: Rahway NJ (Hybrid role - onsite 3 days per week required)Functional Area: Regulatory Innovation and Information Management (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS)The Associate Director of R...

Valencia CA RemoteSenior Specialist International Regulatory Affairs The Senior Professional Regulatory Affairs implements and monitors regulatory programs and assists in the homologation of the product range.The Senior Regulatory Affairs (RA) Specialist - International will plan and execute global...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

The Senior Manager Regulatory Affairs Device works with internal and external partners to deliver products to patients. Prepares device regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions including INDs/CTAs and amendments new mark...