QA Inspector — GMP/GDP for Medical Devices

1 DexCom Inc; Colorado; On-site; USD 58,410,000 - 87,891,000; Full time

Benefits offered by this job

Benefits program

Career development

Tuition reimbursement

Job summary

Dexcom is seeking a Quality documentation specialist to support the Quality team in maintaining GDP-compliant, accurate manufacturing records. You will review in-process and final docs, ensure labels meet standards, and assist with line clearances and GDP audits.

You will also participate in NCMR processes, in-process inspections, and training for new staff, adapting to a fast-paced, regulated environment with cross-functional collaboration.

Qualifications

• Minimum 2–4 years of related experience in a regulated environment.
• HS diploma or equivalent required; related certifications preferred.
• Experience with GDP, documentation control, and quality inspections.

Responsibilities

• Perform in-process and final document reviews for GDP compliance.
• Inspect labels and packaging to verify quality standards.
• Review manufacturing line clearances and participate in GDP audits.
• Support NCMR processes and in-process product inspections.
• Train new employees on quality processes and procedures.

Skills

GDP compliance

Documentation accuracy

Quality audits

Agile/PLM

Microsoft Office

Education

High School diploma

Tools

Oracle

Camstar

PLM

Job description

Dexcom is seeking a Quality documentation specialist to support the Quality team in maintaining GDP-compliant, accurate manufacturing records. You will review in-process and final docs, ensure labels meet standards, and assist with line clearances and GDP audits.

You will also participate in NCMR processes, in-process inspections, and training for new staff, adapting to a fast-paced, regulated environment with cross-functional collaboration.