Global Regulatory Jobs in Carlsbad, CA

Job Description Summary#LI-Hybrid #LI-OnsiteIn this role you will be a part of the Regulatory team within Navigate and will be primarily responsible for providing strategic product direction as well as directing and coordinating the submission of regulatory documents for regulated IV More...

The Director Clinical Operations will ensure that clinical stage programs achieve program objectives within established timelines budget and quality standards. This role involves contributing to the development of clinical program strategy providing leadership to the clinical operatio More...

PurposeThe Global Project Lead is a pivotal and influential role within our organization responsible for shaping and supporting the clinical pipeline with a strategic focus on the analytical testing domain. This role is paramount in providing comprehensive governance over the method l More...

Job Description:Summary: The Design Quality Engineer position is responsible to implement and lead Design Quality Engineering activities at the DJO design and production location(s) as assigned. The Design Quality Engineer will support priority Product Development and Sustaining Desig More...

We anticipate the application window for this opening will close on - 1 Aug 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 mo More...

BandLevel 4Job Description Summary#LI-Hybrid #LI-OnsiteIn this role you will be a part of the Regulatory team within Navigate and will be primarily responsible for providing strategic product direction as well as directing and coordinating the submission of regulatory documents for r More...

The Associate Director works independently with guidance from a Director and is responsible for developing and implementing the HEOR strategy and tactics supporting more than one indication within the same product or more than one product within the same indication either US or Intern More...

The Associate Director works independently with guidance from a Director and is responsible for developing and implementing the HEOR strategy and tactics supporting more than one indication within the same product or more than one product within the same indication either US or Intern More...

The Director Health Economics & Outcomes Research (OUS) leads the development & execution of projects for on-market and/or pipeline development assets who is the brand/asset leader representing HEOR on cross functional asset/brand teams and in the pipeline commercialization te More...

Sobi is seeking a highly experienced passionate and collaborative Director of Strategic Accounts (DSA) to cover a regional geographic market (NY Metro and surrounding areas) reporting into one of two commercial Strategic Account Leads (East/West). This critical role focuses on the lau More...

Step into a role where your regulatory expertise helps bring life-enhancing medical technologies to market. My client is seeking a driven Senior Regulatory Affairs Associate to support U.S. and global submissions for innovative devices developed in Carlsbad CA. Your work will directly More...

The Director Health Economics & Outcomes Research (OUS) leads the development & execution of projects for onmarket and/or pipeline development assets who is the brand/asset leader representing HEOR on cross functional asset/brand teams and in the pipeline commercialization tea More...

The Associate Director works independently with guidance from a Director and is responsible for developing and implementing the HEOR strategy and tactics supporting more than one indication within the same product or more than one product within the same indication either US or Intern More...

The Associate Director Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading crossfunctional multidisciplinary therapeutic teams and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace More...

About This Role:As the Senior Director of Medical Affairs Statistics you will play a pivotal role in leading a dynamic team focused on evidence generation and health technology assessment. This position is critical to ensuring the development and dissemination of scientific evidence o More...

Work ScheduleStandard (MonFri)Environmental ConditionsOfficeJob DescriptionResponsibilities:Join Thermo Fisher Scientific Inc. as a Manager Regulatory Affairs and play a pivotal role in molding our regulatory strategies!Responsible for providing guidance to ensure that all regulatory More...

About This Role:As a Senior Medical Director for Alzheimers disease & Dementia (ADD) Clinical Development you will be at the helm of pioneering programs that have the potential to transform lives. Youll lead and oversee clinical development activities across both early and latesta More...

Job DescriptionJob Summary:We are seeking an experienced and highly motivated Business Analyst with a strong background in Veeva RIM and regulatory publishing processes. The ideal candidate will bring solid business analysis expertise including requirements elicitation documentation a More...

Job DescriptionJob Summary:The Manager (contractor) will be part of Analytical Science and Technology (ASAT) team within Commercial Manufacturing & Supply Chain (CMSC) department. S/He/They will provide support with development and of the analytical CMC strategy by contributing t More...