Quality Control Technician

Harba; St. Louis (MO); On-site; USD 40,000 - 55,000; Full time

Job summary

Harba, located in St. Louis, Missouri, is seeking a Laboratory Technician to perform routine testing of materials and ensure compliance with quality standards. The ideal candidate will hold an Associate’s or Bachelor’s degree in a relevant life science field and have some experience in a laboratory setting.

The role involves preparing test samples, conducting analyses, and maintaining meticulous records in accordance with cGMP regulations.

Qualifications

• 0–3 years of laboratory experience in a pharmaceutical or GMP-regulated environment preferred.
• Familiarity with laboratory analytical techniques and quality control procedures.
• Knowledge of cGMP regulations, laboratory documentation practices, and data integrity requirements.

Responsibilities

• Perform routine laboratory testing of raw materials, in-process samples, and finished products.
• Conduct chemical, physical, or microbiological tests depending on product and process requirements.
• Prepare samples, reagents, and test solutions according to SOPs.

Skills

Laboratory analytical techniques

Quality control procedures

Knowledge of cGMP regulations

Education

Associate’s or Bachelor’s degree in Chemistry, Biology, Microbiology, Biotechnology, or a related life science field

Job description

Job Responsibilities

• Perform routine laboratory testing of raw materials, in-process samples, and finished products using established analytical methods.
• Conduct laboratory analyses such as chemical, physical, or microbiological tests depending on product and process requirements.
• Prepare samples, reagents, and test solutions in accordance with Standard Operating Procedures (SOPs).
• Accurately record test results and laboratory activities in logbooks, worksheets, or electronic systems in compliance with cGMP and data integrity requirements.
• Operate and maintain laboratory equipment, ensuring proper calibration and qualification status.
• Review test data and report any out-of-specification (OOS) or abnormal results to supervisors.
• Assist with laboratory investigations, deviations, and corrective and preventive actions (CAPA) when required.
• Maintain laboratory cleanliness, organization, and compliance with safety and quality standards.

Qualifications

• Associate’s or Bachelor’s degree in Chemistry, Biology, Microbiology, Biotechnology, or a related life science field.
• 0–3 years of laboratory experience in a pharmaceutical, or GMP-regulated environment preferred.
• Familiarity with laboratory analytical techniques and quality control procedures.
• Knowledge of cGMP regulations, laboratory documentation practices, and data integrity requirements.