Quality Technician: GMP QA & Compliance | 3 Weeks PTO

Intiva Health; Chandler (AZ); On-site; USD 42,000 - 54,000; Full time

Benefits offered by this job

3 weeks PTO

Friendly environment

Monthly supplements provided

Job summary

Gummi World in Chandler, AZ is hiring a Quality Technician to perform hands-on quality control across production, bottling, and sanitation processes. You will ensure compliance with 21 CFR Part 111, GMP, and regulatory SOPs through thorough documentation and clear communication with production and management.

The role involves sampling, labeling checks, deviation reporting, and daily walk-throughs to support CAPA investigations and audits. A science-related degree and GMP training are preferred.

Qualifications

• Associate or Bachelor’s degree in a science-related field is preferred.
• cGMP, HACCP, and Food Safety training or certification is preferred.
• Proficient in MS Excel and MS Word; strong attention to detail and communication skills.

Responsibilities

• Perform weight checks and inspect product appearance, monitor water activity.
• Verify labels, lot numbers, expiration dates, seal integrity, packaging quality, and fill levels.
• Report deviations to the Quality Team and assist with CAPA investigations.
• Collect raw material and finished product samples; complete forms and communicate status.
• Conduct ATP swab testing and verify sanitation before production begins; monitor key process parameters.
• Complete QA sections of batch records, logbooks, and forms per GMP; support audits.

Skills

Quality control

Documentation

Regulatory compliance

Attention to detail

Communication

Education

Associate or Bachelor’s degree in a science-related field

Tools

MS Excel

MS Word

Job description

Gummi World in Chandler, AZ is hiring a Quality Technician to perform hands-on quality control across production, bottling, and sanitation processes. You will ensure compliance with 21 CFR Part 111, GMP, and regulatory SOPs through thorough documentation and clear communication with production and management.

The role involves sampling, labeling checks, deviation reporting, and daily walk-throughs to support CAPA investigations and audits. A science-related degree and GMP training are preferred.