Dexcom
Sr QA Engineer – Dexcom
Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM).
For 25 years Dexcom has worked to transform how diabetes is managed by providing actionable insights to improve health outcomes and now seeks to expand beyond diabetes to empower people to take control of health worldwide.
Where You Come In
You work as a QA engineer of the Product Development Team within the R&D Department, assisting with defining design inputs, designing components and processes, verifying design outputs, and validating user needs.
You develop processes and perform quality functions to help reconcile quality policy requirements and regulatory compliance—including supporting CAPAs, Post‑Market Surveillance, Biocompatibility, Sterilization, and Electrical Safety.
You analyze reports and data to identify trends and recommend updates or changes to quality standards and procedures.
You ensure compliance to external specifications and standards.
You develop company policies and procedures that support compliance with domestic and international regulations.
You execute risk management, validation, sample‑size, and external‑standard review and implementation activities.
You develop systems and processes that improve product safety, process efficiency, consistency of product conformance, and reduce waste.
What Makes You Successful
Knowledge in medical device design control, especially planning, inputs, verification, validation, change, risk management, biocompatibility, sterilization, and electrical safety.
Ability to adapt to new responsibilities, projects, processes, and industry changes.
Experience writing documentation in the medical device or related industry and demonstrating compliance with CFR, EU MDR, ISO 13485, and related standards.
Strong collaboration and influence through verbal & written communication.
Analytical skills, including the use of statistical methods to analyze data.
Proficiency in interpreting technical procedures, international standards, and government regulations to assure safety and high performance.
What You’ll Get
A front‑row seat to life‑changing CGM technology and Dexcom’s 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, innovative, industry‑leading organization committed to its employees, customers, and communities.
Experience and Education
Bachelor’s degree in a technical discipline with 5–8 years of related experience, or Masters degree with 2–5 years of equivalent experience, or PhD with 0–2 years of experience.
Flex Workplace Your primary location will be a home office. You will collaborate with your manager to determine office visit needs. You must live within commuting distance of your assigned Dexcom site (typically 75 miles / 120 km).
Equal Opportunity Employer Dexcom is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at talentacquisition@dexcom.com.
Salary $87,000.00 – $145,000.00
Job Details
Seniority level: Not Applicable
Employment type: Full‑time
Job function: Engineering and Information Technology
Industries: Medical Equipment Manufacturing
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For 25 years Dexcom has worked to transform how diabetes is managed by providing actionable insights to improve health outcomes and now seeks to expand beyond diabetes to empower people to take control of health worldwide.
Where You Come In
You work as a QA engineer of the Product Development Team within the R&D Department, assisting with defining design inputs, designing components and processes, verifying design outputs, and validating user needs.
You develop processes and perform quality functions to help reconcile quality policy requirements and regulatory compliance—including supporting CAPAs, Post‑Market Surveillance, Biocompatibility, Sterilization, and Electrical Safety.
You analyze reports and data to identify trends and recommend updates or changes to quality standards and procedures.
You ensure compliance to external specifications and standards.
You develop company policies and procedures that support compliance with domestic and international regulations.
You execute risk management, validation, sample‑size, and external‑standard review and implementation activities.
You develop systems and processes that improve product safety, process efficiency, consistency of product conformance, and reduce waste.
What Makes You Successful
Knowledge in medical device design control, especially planning, inputs, verification, validation, change, risk management, biocompatibility, sterilization, and electrical safety.
Ability to adapt to new responsibilities, projects, processes, and industry changes.
Experience writing documentation in the medical device or related industry and demonstrating compliance with CFR, EU MDR, ISO 13485, and related standards.
Strong collaboration and influence through verbal & written communication.
Analytical skills, including the use of statistical methods to analyze data.
Proficiency in interpreting technical procedures, international standards, and government regulations to assure safety and high performance.
What You’ll Get
A front‑row seat to life‑changing CGM technology and Dexcom’s 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, innovative, industry‑leading organization committed to its employees, customers, and communities.
Experience and Education
Bachelor’s degree in a technical discipline with 5–8 years of related experience, or Masters degree with 2–5 years of equivalent experience, or PhD with 0–2 years of experience.
Flex Workplace Your primary location will be a home office. You will collaborate with your manager to determine office visit needs. You must live within commuting distance of your assigned Dexcom site (typically 75 miles / 120 km).
Equal Opportunity Employer Dexcom is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at talentacquisition@dexcom.com.
Salary $87,000.00 – $145,000.00
Job Details
Seniority level: Not Applicable
Employment type: Full‑time
Job function: Engineering and Information Technology
Industries: Medical Equipment Manufacturing
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