Associate Regulatory Affairs Specialist

Dexcom • San Diego, CA

114d • $28 - $47

About The Position

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 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.

Requirements

• Typically requires a Bachelor's degree and 0-2 years previous experience.
• Strong written and verbal communication skills.
• Ability to team with others to complete work objectives.
• Ability to find and implement solutions to sometimes complex challenges.
• Motivated by working at a fast pace.
• Interest in, or familiarity with, the healthcare industry.
• Experience with the medical device or biopharmaceutical industry is highly desired.
• Demonstrated interest in diabetes is a huge plus.
• Highly flexible and able to shift priorities as needed.
• Self-starter with exceptional interpersonal skills.

Responsibilities

• Help develop regulatory content for use in submissions and reports.
• Provide assistance in the completion of specific regulatory and clinical evaluation deliverables.
• Perform regulatory research, recommending process improvements, developing improvement plans, implementing, and tracking results.
• Assisting with RA PMO project planning activities and reporting.
• Maintain regulatory documentation.
• Organize regulatory files.
• Track tasks to ensure completion.
• Perform tasks or projects under the direct supervision of RA management or specialists.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Computer and Electronic Product Manufacturing
• Education Level: Bachelor's degree