Aseptic QC Micro Tech II — Environmental Monitoring

Frontdoor Defense; Ohio; On-site; USD 30,000 - 41,000; Full time

Benefits offered by this job

401(k) with company match

Healthcare benefits (medical, dental,视

Paid vacation and holidays

Tuition reimbursement

Job summary

Resilience is seeking a Quality Technician II for QC Micro – Aseptic Control in West Chester Township, Ohio. This role handles environmental monitoring and microbial sampling in aseptic environments to support sterile manufacturing, with cGMP documentation and strict compliance.

The position requires following SOPs, maintaining accurate records, and collaborating across teams. The role supports training and may require 24/7 on-call availability as needed.

Qualifications

• Follow written procedures, SOPs and work instructions with minimal supervision.
• Strong attention to detail and ability to maintain accurate records.
• Read, write, speak, and follow English instructions.
• High school diploma or equivalent.
• 1+ years in pharmaceutical, biotechnology, or cGMP manufacturing.
• Experience with environmental monitoring software (MODA, LIMS, Novatek) preferred.

Responsibilities

• Document activities, actions, and results per documentation practices; read SOPs and maintain records.
• Perform visual inspections and routine sampling using Environmental Monitoring System with data entry.
• Follow SOPs and cGMP work instructions; perform lab duties accordingly.
• Maintain clean, compliant work area and report deviations to supervisor.
• Audit SOPs and work instructions; suggest improvements for compliance.
• Support training of new technicians.

Skills

Attention to detail

Procedural adherence

English proficiency

Education

High school diploma or equivalent

Tools

Microsoft applications

MODA

LIMS

Novatek

Job description

Resilience is seeking a Quality Technician II for QC Micro – Aseptic Control in West Chester Township, Ohio. This role handles environmental monitoring and microbial sampling in aseptic environments to support sterile manufacturing, with cGMP documentation and strict compliance.

The position requires following SOPs, maintaining accurate records, and collaborating across teams. The role supports training and may require 24/7 on-call availability as needed.