Quality Assurance, Aseptic Technician

Title: QA Aseptic Technician

Location: West Chester OH

Shifts available:

• Night shift 12 hour rotating, 6PM– 630AM – days off vs days worked will vary week to week

Rate: $23-24/hour

Duration: 6-12 months, possibility of being extended or becoming permanent

About the Role

We are seeking a detail-oriented Quality Technician I to support environmental monitoring activities within our sterile pharmaceutical manufacturing facility. In this role, you will work independently in both classified (up to Class 100) and non-classified environments to ensure all processes meet cGMP and regulatory expectations. This position is essential to maintaining a safe, compliant, and high-performing aseptic production environment.

What You’ll Do

• Perform routine environmental monitoring and sample collection in aseptic areas.

• Accurately document all activities and results following Good Documentation Practices.

• Maintain complete laboratory records, quality records, and sample receipts.

• Read and follow SOPs, diagrams, and technical documentation.

• Conduct visual inspections and support cross-functional operational needs.

• Guide team members on SOPs and work instructions; help coordinate support activities.

• Ensure adherence to cGMP and aseptic techniques across laboratory operations.

• Perform SOP/work instruction audits and assist with continuous compliance improvements.

• Wear required gowning, sterile garments, and PPE in cleanroom environments.

• Provide occasional 24/7 on-call support.

• Communicate quality or service concerns promptly and constructively.

What You Bring

Minimum Requirements

• Experience working in a pharmaceutical production environment, clean room setting, tissue manufacturing, or hospital operations.

• Ability to read, write, and communicate effectively in English.

• Strong attention to detail and accuracy.

• Ability to perform basic mathematical calculations.

Preferred Qualifications

• High school diploma, vocational certification, or equivalent required; degree preferred.

• Familiarity with MODA, Microsoft Office, SAP, and KRONOS.

• Experience with LEAN manufacturing practices.

• Knowledge of cGMPs and FDA regulations.

Who You’ll Work With

• Quality Control teams

• Operations and production staff

Physical & Work Environment Requirements

• Ability to work in cleanroom and aseptic environments with full gowning/PPE.

• Ability to stand, perform repetitive tasks, and complete time-sensitive activities.

• Regular, reliable attendance and collaboration with cross-functional teams.

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