QC Tech Essay

Job Id: 263361

QC Tech Essay
Location: Carlsbad CA
Schedule: Monday through Friday 5:30 AM to 2:00 PM
Shift: 1st Shift
Duration: 1 year contract
Pay Rate: $19.50 per hour

Position Summary

The Quality Control Technician is responsible for performing Quality Control testing on products at various stages of production. This includes routine SOP testing special assignments and accurate documentation of findings for Device History Records.

This role supports core QC Chemistry functions including Stability Studies Raw Material Testing Proficiency Testing and Customer Complaint investigations. The ideal candidate is detail oriented organized and comfortable working in a regulated laboratory and manufacturing environment.

Key Responsibilities

• Perform and document QC Sofia testing of work in process production lots

• Conduct first article functional Sofia final kit QC testing

• Support daily QC Chemistry core functions as needed

• Assist with new product development and product improvement projects

• Maintain accurate documentation in accordance with GMP and quality standards

• Attach test results to Device History Records accurately and timely

• Operate laboratory equipment safely and in accordance with established procedures

• Maintain laboratory organization and housekeeping standards

• Communicate testing results with Manufacturing and cross functional teams to support production timelines

• Train new Quality Control Technicians as needed

• Carry out duties in compliance with established business policies and quality systems

Work Environment

This role operates in a laboratory manufacturing and office environment. Responsibilities may include handling viral or bacterial materials hazardous chemicals and potentially infectious samples.

Strict adherence to safety procedures quality regulations and required Personal Protective Equipment is mandatory.

Physical Requirements

• Ability to lift up to 20 pounds regularly

• Up to 90 percent of time spent at a lab bench or desk

• Prolonged standing walking and sitting

• Ability to operate laboratory equipment

• Close and distance vision with ability to adjust focus

Qualifications

• Bachelor’s degree in Chemistry Biology Life Science or related field preferred

• 0 to 2 years of experience in a Quality Control or manufacturing laboratory environment

• Experience in medical device or high volume manufacturing preferred

• Understanding of QSR and ISO regulations

• General chemistry and laboratory skills with GLP or GMP experience

• Strong written and verbal communication skills

• Proficient with data entry and spreadsheet navigation

• Knowledge of quality terminology and traceability concepts

• Ability to prioritize workload and work independently

• Strong problem solving and decision making skills