QA Inspector II

HireLifeScience; California (MO); On-site; USD 29,000 - 41,000; Full time

Benefits offered by this job

Paid time off

Health/Dental/Vision

Flexible spending accounts

Retirement benefits

Job summary

HireLifeScience is seeking a QA Inspector II to oversee daily QA inspection activities for finished products and sub-assemblies. You will interpret drawings, BOMs, specs, and POs to determine quality status and support manufacturing, while training new hires and ensuring adherence to SOPs.

You will review batch records, prepare documentation, initiate NCMRs for non-conforming materials, and maintain accurate QA records in SAP, contributing to a compliant, efficient bioprocessing environment.

Qualifications

• High School Diploma, GED, or equivalent.
• 3–5 years of quality inspection experience in a laboratory or manufacturing setting.
• Ability to work independently after training.
• Experience with ISO 9001, ISO 13485, 21CFR820 or equivalent QMS.
• Knowledge of AQL inspection plans.

Responsibilities

• Performs in-process finished goods and final inspection including visual inspection.
• Verification of components to engineering records and documentation requirements.
• Access and interpret engineering drawings, bill of materials, specifications, and purchase orders to determine quality status and support manufacturing.
• Prepare, print, and verify documentation and labels for quality and manufacturing process.
• Review manufacturing batch records against applicable quality requirements and document results of inspections.
• Train new hires.
• Identify and clearly communicate nonconformances to specified requirements to Management in timely manner.
• Proficiently use applicable software to accurately document and maintain the QA inspection process.
• Support completed batch records scanning and records retention.
• Initiate NCMRs for non-conforming materials and assist in investigations for deviations, CA, etc.
• Ensure compliance to current SOP’s and Work Instructions and suggest enhancements to procedures.
• Review Lot History Records (LHR) for release of finished products and sub-assemblies in SAP.
• Adhere to all company Quality policies and procedures.

Skills

Detail oriented

Communication

Independent work

QMS standards knowledge

AQL inspection plans

Education

High School Diploma, GED, or equivalent

Tools

SAP

Job description

The QA Inspector II will report directly to the QA Supervisor or QA Manager.

This role is responsible for the oversight of all daily QA inspection activities, of finished products and sub-assemblies.

This role is expected to model our Leadership Behaviors-Integrity & Compliance, Customer Focus, Collaboration, Courage, Team Empowerment, and Accountability & Results-in all aspects of work.

• Performs in-process finished goods and final inspection including visual inspection.
• Verification of components to engineering records and documentation requirements.
• Access and interpret engineering drawings, bill of materials, specifications, and purchase orders to determine quality status and support manufacturing.
• Prepare, print, and verify documentation and labels for quality and manufacturing process.
• Review manufacturing batch records against applicable quality requirements and document results of inspections.
• Train new hires.
• Identify and clearly communicate nonconformances to specified requirements to Management in timely manner.
• Proficiently use applicable software to accurately document and maintain the QA inspection process.
• Support completed batch records scanning and records retention.
• Initiate NCMRs for non-conforming materials and assist in investigations for deviations, CA, etc.
• Ensure compliance to current SOP’s and Work Instructions and suggest enhancements to procedures.
• Review Lot History Records (LHR) for release of finished products and sub-assemblies in SAP.
• Adhere to all company Quality policies and procedures.

Qualification

• High School Diploma, GED, or equivalent with 3 to 5 years of Quality Inspection required.
• Laboratory or manufacturing setting work experience within a controlled Quality environment preferred.
• Ability to work independently once training has been completed.
• Ability to communicate with multiple departments.
• Detail oriented to all aspects of daily activities.
• Experience with ISO 9001, ISO 13485, 21CFR820 or equivalent QMS standards.
• Maintain a positive and team-oriented attitude with good organizational skills.
• Good written and verbal communication skills.
• Knowledge of AQL Inspection Plans

Our mission is to inspire advances in bioprocessing as a trusted partner in the production of biologic drugs that improve human health worldwide. Focused on cost and process efficiencies, we deliver innovative technologies and solutions that help set new standards in bioprocessing. The estimated hourly rate for this role, based in the United States of America is between $20.80/Hr - $29.90/Hr. Compensation decisions are dependent on several factors including, but not limited to an individual's qualifications, location, internal equity, and alignment with market data.

We offer a wide range of benefits such as paid time off, health/dental/vision, retirement benefits and flexible spending accounts. All compensation and benefits information will be confirmed in writing at the time of offer.