Quality Control Technician - Pharma QC & Growth

STAQ Pharma Inc; Denver (CO); On-site; USD 27,000 - 39,000; Full time

Benefits offered by this job

Health insurance

401(k) matching

PTO

Holidays

Professional growth

Job summary

STAQ Pharma Inc in Denver, CO is seeking a Quality Control Technician to support the QC function in a 503B pharmaceutical manufacturing environment, ensuring materials, samples, documentation, and environmental monitoring meet cGMP and regulatory requirements.

The role involves hands-on QC, QA, and operations support, sample preparation, external lab submissions, logbooks, inspection activities, and contributing to investigations and continuous improvement while maintaining accurate records and

Qualifications

• Associate degree in the sciences or equivalent experience preferred.
• At least 1 year of Quality Control Technician experience preferred.
• Pharmaceutical, medical device, biotechnology, laboratory, sterile manufacturing, or regulated manufacturing experience preferred.
• Familiarity with cGMP, GDP, FDA-regulated environments, quality documentation, or controlled procedures preferred.
• Strong attention to detail and ability to review records, forms, and logs for completeness and accuracy.

Responsibilities

• Coordinate QC sample preparation and shipment/submission to external laboratories for various testing activities.
• Support environmental monitoring and microbiological sample evaluation activities.
• Maintain retention materials and organize documentation related to QC activities.
• Review GMP documents, room logs, equipment logs, and quality records for accuracy.
• Support investigations, deviations, CAPAs, and continuous improvement efforts.

Skills

Attention to detail

Team player

Communication skills

Independent judgment

English proficiency

Education

Associate degree

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Outlook

Job description

STAQ Pharma Inc in Denver, CO is seeking a Quality Control Technician to support the QC function in a 503B pharmaceutical manufacturing environment, ensuring materials, samples, documentation, and environmental monitoring meet cGMP and regulatory requirements.

The role involves hands-on QC, QA, and operations support, sample preparation, external lab submissions, logbooks, inspection activities, and contributing to investigations and continuous improvement while maintaining accurate records and