QA Coordinator – 2nd Shift (Manufacturing)

vwr; Paris (KY); On-site; USD 42,000 - 63,000; Full time

Job summary

Avantor seeks a Quality Assurance Coordinator to join the Quality Department at our Paris, KY facility, working second shift Monday–Friday 3:30pm–12:00am EST.

You will execute QA processes, inspections, and documentation reviews to ensure product quality and regulatory compliance, coordinating with Manufacturing, suppliers, and auditors.

Strong knowledge of FDA regulations and cGMP, plus SAP experience, is preferred; excellent attention to detail and ability to manage multiple priorities.

Qualifications

• High School completion or GED required.
• Experience in quality assurance within a manufacturing environment preferred.
• Familiar with FDA regulations and cGMP requirements.
• Strong familiarity with regulatory and quality assurance procedures, systems, and operations.

Responsibilities

• Match MPOs and bench sheets for finished goods and perform audits of job packets
• Release materials in IMS and maintain MPO audit logs, including audit metrics and results
• Maintain filing and storage of quality records
• Print, cut, count, verify, package, and issue label packets according to production schedules
• Issue packaging jobs to production
• Maintain the stability storage area and collect monthly stability samples
• Perform internal audits as scheduled
• Maintain inventory quality status and support MRB activities
• Manage hazardous and universal waste in accordance with local, state, and federal regulations
• Perform other duties as assigned, with or without accommodation

Skills

Interpersonal skills

Time management

Communication skills

Attention to detail

Initiative & accountability

Independent work

Professional judgment

Software proficiency

Education

High School diploma or GED

Tools

Microsoft Office

SAP

Job description

Avantor seeks a Quality Assurance Coordinator to join the Quality Department at our Paris, KY facility, working second shift Monday–Friday 3:30pm–12:00am EST.

You will execute QA processes, inspections, and documentation reviews to ensure product quality and regulatory compliance, coordinating with Manufacturing, suppliers, and auditors.

Strong knowledge of FDA regulations and cGMP, plus SAP experience, is preferred; excellent attention to detail and ability to manage multiple priorities.