Regulatory Affairs Officer Jobs in USA

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...

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...

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...

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...

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 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...

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...

The Director Regulatory Affairs is responsible for leading the development and execution of regulatory strategies for assigned assets ensuring alignment and execution across regions. This role collaborates closely with other regulatory team members to prepare and manage submissions leads interaction...

Location: Palo Alto CA / Miami FL / Princeton NJ onsite or REMOTE USAbout Summit:Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life increasing potential duration of life and resolving serious unmet medical needs. At Summit we believe...

Location: Palo Alto CA / Miami FL / Princeton NJ onsite or REMOTE USAbout Summit:Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life increasing potential duration of life and resolving serious unmet medical needs. At Summit we believe...

Bring more to life.Are you ready to accelerate your potential and make a real difference within life sciences diagnostics and biotechnologyAt Cepheid one of Danahers 15 operating companies our work saves livesand were all united by a shared commitment to innovate for tangible impact.Youll thrive in...

Your missionReporting to the Chief Executive Officer of Pierre Fabre Pharmaceuticals (PFP) theVice President of Regulatory Affairs (RA) and Pharmacovigilance (PV)is a vital member of PFPs leadership team and of the Global Regulatory Affairs organization. This role involves overseeing all regulatory...

Location: Palo Alto CA / Miami FL / Princeton NJ onsiteAbout Summit:Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life increasing potential duration of life and resolving serious unmet medical needs. At Summit we believe in building a...

We anticipate the application window for this opening will close on - 28 Nov 2025At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected c...