×
Register Here to Apply for Jobs or Post Jobs. X

QA Engineer - Chemistry Focus

Job in San Diego, San Diego County, California, 92189, USA
Listing for: Dexcom Deutschland GmbH
Full Time position
Listed on 2026-01-13
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering
Job Description & How to Apply Below
Position: Staff QA Engineer - Chemistry Focus

Staff QA Engineer - Chemistry Focus
San Diego, California

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.

Meet The Team

Join us in empowering people to take control of their health! You will join a collaborative team at the heart of Dexcom’s products. Our quality engineering team plays a crucial role in cross‑site and cross‑functional alignment for the future of Dexcom and for the future of health. You will support Dexcom in launching state‑of‑the‑art innovative technology and will help define, support, and improve the processes that get us there.

Where

You Come In
  • You offer expertise in chemistry, polymers/polymer manufacturing, scale‑up, and/or analytical test method validation, including but not limited to GPC, HPLC, FTIR.
  • You apply your hands‑on experience with high volume manufacturing in medical device, biosensor, or similarly regulated industry and are seen as a quality leader, performing strategic work with minimal direction needed from management.
  • You provide leadership and technical guidance for strengthening of and adherence to the Quality Management System (Failure Mode Effects Analysis (FMEA), qualification and validation requirements, CAPAs, NCMRs, Process Controls).
  • You lead multi‑level, cross‑functional, and international cross‑site alignment on complex scientific topics and provide direction with strong critical thinking and excellent personal and communication (written and oral) skills.
  • You create strong partnerships with R&D, Regulatory Affairs, Customer Advocacy, Process Engineering, Manufacturing, Equipment Engineering, Maintenance teams and more.
  • You apply your expertise in risk‑based decision‑making to manage Risk/Impact assessments during various phases of design controls (use of novel materials, change control, validation, monitoring plans, sampling plans, sample size, non‑conformances), providing solutions that align with risk.
  • You support root cause analysis, six sigma, structured problem solving, Test Method Validation (including but not limited to Gage R&R), software validation, process capability measurement (Cpk), lean manufacturing, and statistical analysis.
  • You take initiative to drive identification, assessment, and corrections/corrective actions/preventive actions for compliance and procedural gaps.
What Makes You Successful
  • Your Chemical Engineering, Chemistry, or similar degree from an accredited college/university and your expertise in biosensors, chemistry, and polymers, and complex analytical methods as they relate to manufacturing and material/process characterization.
  • Your familiarity with Medical Device, Pharmaceutical and/or Combination Product requirements, e.g. 21 CFR 4, 10, 11, and 820, USP, ISO 13485, EU MDR.
  • Your Six Sigma, Lean manufacturing, and/or sustaining experience supporting process characterization and improvements.
  • Your expertise with quality engineering tools for statistical data analysis, sampling plan development, sample size determination, AQL, confidence intervals, etc.; statistical software (e.g. JMP) experience and six sigma green belt certification(s) preferred.
  • Your competency…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary