Regulatory Affairs Specialist
$71.6k - $119.3kDexcom
Dexcom CorporationDexcom 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 later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.Meet the team:Regulatory Affairs is a team of more than 40 professionals located either at San Diego HQ or remotely around the globe. Our backgrounds range from biological and physical sciences to engineering, political science to biostatistics, pharmacology to law just to name a few. Our degrees include Bachelor's, Master's, Ph.D.'s, JD's and more. With our various backgrounds and talents we help to navigate and align the ideas and output of most facets of the company to successfully get our home-use products to our end users. We're closely connected with QA, Clinical, IT, and Global Business Solutions (GBS) under the same Executive Vice President. At our quarterly onsite gatherings, some of our pastimes include story sharing, cooking and baking, social events and other team-building activities.If you join our team you will be supporting the growth and expansion of Dexcom's Continuous Glucose Monitoring (CGM) Systems.Where you come in:You will support developmental activities for Dexcom software products.You will develop regulatory strategies and prepare submissions in various countries (US, EU, Canada).You will collaborate with regional regulatory teams to develop global strategies as required.You will review and approve product and promotional labeling for software.You will represent Regulatory Affairs on various cross-functional software teams.You will review and approve software documentation and evaluate for submission requirements.You will take on additional projects and responsibilities as needed.What makes you successful:You bring knowledge of US and international regulatory requirements including design control, medical device submission requirements, labeling and promotion regulations, and medical device quality systems.You have Medical Device Software experience and/or knowledge, such as software development lifecycle, IEC 62304, and software classification.You have strong technical writing, editing, and analytical skills.You work well independently and with cross-functional teams.You thrive in a fast-paced environment and adapt quickly to changing priorities.You are proficient in problem solving, proactive learning, organization, and have excellent communication skills.Having previous experience with 510(k) submissions, Health Canada submissions, or EU Medical Device Regulation is preferred.What you'll get:A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.A full and comprehensive benefits program.Growth opportunities on a global scale.Access to career development through in-house learning programs and/or qualified tuition reimbursement.An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.Travel Required:5-15%Experience and Education Requirements:Typically requires a Bachelor's degree and a minimum of 2-5 years of related experience.Flex Workplace:Your primary location will be a home office. You will not have an assigned workstation and will work with your manager to determine office visit needs. You must live within commuting distance of your assigned Dexcom site (typically 75 miles/120km).Salary:$71,600.00 - $119,300.00#DexcomUS
- ...US Regulatory Affairs LeadScope of Responsibilities:He/She will be responsible for representing regulatory function to approve promotional material. He/She will be at ease working in a matrix environment and be able to navigate ambiguity to drive decision making working...Suggested
$71.6k - $119.3k
...company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us. Meet The Team Regulatory Affairs is a team of more than 40 professionals located either at San Diego HQ or remotely around the globe. Our backgrounds range...SuggestedWork at officeRemote workWorldwideHome officeFlexible hours$91.7k - $137.53k
Job SummaryPosition Overview: The Senior Regulatory Affairs Specialist will lead activities which support both domestic and international regulatory registrations and submissions activities including working with Marketing, New Product Development, Manufacturing and Engineering...SuggestedFull timeWork at office$105.8k - $132.25k
Regulatory Affairs Specialist 3 - Medical Device IVD Location: CA-San Diego, US Contract Type: Regular Full-Time Area: TECHNICAL Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of...SuggestedFull timeContract workWork at officeLocal area- Senior Regulatory Affairs Specialist - Medical Devices Clinical San Diego , California Contract Aug 10, 2026 Senior Regulatory Affairs Specialist - Medical Devices Position Overview Viltis is seeking an experienced Senior Regulatory Affairs Specialist to support a leading...SuggestedContract work
$105.8k - $132.25k
A global healthcare company is seeking a Regulatory Affairs Specialist III in San Diego, CA. This role focuses on ensuring regulatory compliance and global market access for in-vitro diagnostic (IVD) products. Candidates must have a Bachelor’s degree and at least 6 years...- Dexcom Inc. is seeking a Regulatory Affairs Specialist to support development activities for our CGM software products and to develop regulatory strategies for submissions worldwide. You will collaborate with regional teams to align global regulatory plans and ensure labeling...Worldwide
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- Dexcom Inc. in San Diego, CA is seeking a Regulatory Affairs professional to support software product development and submissions in the US, EU, and Canada. You will partner with cross-functional teams to develop regulatory strategies and ensure compliant labeling and...
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- Dexcom Corporation is seeking a Regulatory Affairs professional to support regulatory activities for Dexcom software products and develop global regulatory strategies for submissions in the US, EU and Canada. You will collaborate with regional teams, review software labeling...Remote job
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$110k - $125k
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ABOUT US Scripps Research is a nonprofit biomedical institute ranked as one of the most influential in the world for its impact on innovation. We celebrated our 100-year legacy in 2024. This significant milestone marks a century of seminal discoveries in immunology, infectious...Contract workWork at officeRemote workFlexible hours1 day per week$45 - $65 per hour
Licensing and Contracts Officer - La Jolla, CA - 4 days onsite, $45-$65/hour Ready to step into a high-impact role supporting cutting-edge innovation? Join an established, research-driven biotech organization’s Office of Technology Development where your expertise in licensing...Hourly payWork at office$72.61k - $101.39k
...programs and Trane Corporate Trade Compliance initiatives for the Americas. Researches trade regulations and rulings, determines regulatory or interpretive basis for each classification, and communicates with internal clients and external service providers. Provide guidance...Hourly payWork at officeLocal areaWork from homeShift work$78k - $98k
...decisions with confidence. Drive compliance strategy : Support and enhance our lending compliance management program, including regulatory change management and risk assessments. Monitor & test : Conduct risk-based reviews, loan file audits, and transaction testing using...Work at office$35 - $45 per hour
...who is detail-oriented, analytical, and eager to contribute to a growing team. Who You Are Experience in compliance, reporting, or regulatory support functions Familiarity with reporting tools or systems used to track and manage data Strong analytical skills with a high...Contract work- ...receipt of military retired pay would be entitled to disability compensation) under laws administered by the Secretary of Veterans Affairs, or was discharged or released from active duty because of a service-connected disability.Recently separated veteran: A veteran separated...
$105.9k - $117k
POSITION SUMMARY:The Animal Program Compliance Specialist is a key member of the Institutional Animal Care and Use Program, responsible... ...and guidance to investigators, research staff, and the IACUC on regulatory requirements and best practices.Reporting to the Director of...Full timeWork at officeFlexible hours$88k - $110k
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...questions in healthcare. Job Type: Full time Job Title: Regulatory & Compliance Specialist Location: Onsite - San Diego Salary Range: $90,000... ...field (e.g., Life Sciences, Engineering, Regulatory Affairs, Quality Management) or equivalent experience....Full time$150k - $195k
...we move toward a common goal of elevating science and service for rare patients.Position Summary:The Associate Director, CMC Regulatory Affairs is responsible for providing strategic and operational regulatory leadership for Chemistry, Manufacturing, and Controls (CMC)...Full timeTemporary workRemote work- JOB SUMMARYThe Associate Director/Director of Regulatory Affairs - Chemistry, Manufacturing and Controls (CMC) will lead global CMC regulatory strategy and execution across Iambic's development programs. The role will prepare and oversee high-quality CMC content for regulatory...Work at officeFlexible hours
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