Quality Inspector II – Precision & GDP Compliance

1 DexCom Inc; Colorado; On-site; USD 52,729,000 - 87,883,000; Full time

Benefits offered by this job

Full benefits program

Career development opportunities

Tuition reimbursement

Job summary

Dexcom is seeking a detail-oriented Quality Documentation Specialist to join the team. You will review in-process and final documents, ensure GDP compliance, and maintain strict quality control across labeling and packaging.

You will conduct audits, support NCMR processes, and train new staff while collaborating with cross-functional teams in a fast-paced regulated environment. Strong attention to detail and process improvement mindset are essential.

Qualifications

• Typically requires 2–4 years of related experience.
• High School diploma or equivalent required.
• Experience in a regulated environment (medical device/pharma) is preferred.
• Strong documentation and GDP knowledge required.

Responsibilities

• Review in-process and final documents for accuracy, GDP compliance, and proper formatting.
• Maintain compliance with procedures and complete required training.
• Inspect labels and packaging for adherence to quality standards.
• Review and approve manufacturing line clearance activities to support product quality.
• Conduct in-process quality audits within manufacturing.
• Assist with Nonconforming Material Report (NCMR) processes.
• Provide training on quality processes to new employees.
• Support additional quality responsibilities as needed.

Skills

Attention to detail

Documentation

Quality standards

Cross-functional teamwork

Problem solving

MS Office

Communication skills

Adaptability

Education

High School diploma or equivalent

Tools

Microsoft Office

Electronic quality systems

Oracle

Camstar

Agile/PLM

Job description

Dexcom is seeking a detail-oriented Quality Documentation Specialist to join the team. You will review in-process and final documents, ensure GDP compliance, and maintain strict quality control across labeling and packaging.

You will conduct audits, support NCMR processes, and train new staff while collaborating with cross-functional teams in a fast-paced regulated environment. Strong attention to detail and process improvement mindset are essential.