QA Aseptic Technician

Kelly Science, Engineering, Technology & Telecom; Olde West Chester (OH); On-site; USD 32,000 - 33,000; Full time

Job summary

Kelly Science, Engineering, Technology & Telecom seeks a Quality Technician II for aseptic control in a sterile pharmaceutical facility. The role supports environmental monitoring in classified and non-classified areas, ensuring cGMP compliance and high quality standards.

The position requires working a 12-hour night rotation on-site in Ohio, with documentation, SOP adherence, and cross-functional teamwork driving continuous improvements in aseptic production.

Qualifications

• Experience in a pharmaceutical production environment or clean room setting.
• Ability to read, write, and communicate effectively in English.
• Strong attention to detail and accuracy.
• Ability to perform basic mathematical calculations.

Responsibilities

• Perform routine environmental monitoring and sample collection in aseptic areas.
• Document activities and results following Good Documentation Practices.
• Maintain laboratory records and sample receipts.
• Read and follow SOPs and technical documentation.
• Conduct visual inspections and support cross-functional operations.
• Guide team members on SOPs and work instructions.
• Ensure adherence to cGMP and aseptic techniques.
• Perform SOP/work instruction audits and support continuous compliance improvements.
• Wear gowning and PPE in cleanroom environments.

Skills

Attention to detail

English communication

Quality control mindset

LEAN manufacturing practices

Education

High school diploma or equivalent

Vocational certification

Tools

MODA

Microsoft Office

SAP

KRONOS

Job description

Title: Quality Technician II, Aseptic Control

• 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 II 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 DoPerform 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.
• 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.