IQC Lead – Materials Inspection & Release

Resilience US; Olde West Chester (OH); On-site; USD 60,000 - 75,000; Full time

Job summary

Resilience US in Ohio seeks an IQC lead to oversee day-to-day inspection, sampling, and testing activities, directing technicians to meet material release goals. You will act as the primary link between IQC and cross-functional teams, ensuring accuracy and compliance with cGMP standards.

You will review data, manage documentation in CMMS/ERP, and drive continuous improvements while collaborating with Supply Chain, Manufacturing, and Quality Assurance to prioritize releases and uphold quality

Qualifications

• Experience in a pharmaceutical or cGXP-regulated environment with ability to self-direct inspections and sampling.
• Effective English communication and meticulous documentation to ensure traceability.
• Proven ability to lead a team of technicians, set priorities, and hold peers accountable.
• Bachelor's degree in business or related discipline preferred; 3+ years in pharma or regulated settings.

Responsibilities

• Plan and execute inspection, sampling, and testing to meet material release schedules.
• Perform visual and physical inspection of incoming materials against specs and drawings.
• Interpret quality standards to determine release readiness and verify labeling and storage.
• Operate and troubleshoot inspection equipment and maintain related records.
• Prepare and maintain cgMP documentation and review data for compliance.
• Use CMMS and ERP systems to track material status and logistics.
• Collaborate with Supply Chain, Manufacturing, and QA to align release priorities.
• Provide on-the-job training and share process knowledge with technicians.

Skills

Leadership

Quality inspection

cGXP compliance

Documentation

English communication

Education

Bachelor's degree in business or related discipline

Tools

CMMS

ERP systems

Job description

Resilience US in Ohio seeks an IQC lead to oversee day-to-day inspection, sampling, and testing activities, directing technicians to meet material release goals. You will act as the primary link between IQC and cross-functional teams, ensuring accuracy and compliance with cGMP standards.

You will review data, manage documentation in CMMS/ERP, and drive continuous improvements while collaborating with Supply Chain, Manufacturing, and Quality Assurance to prioritize releases and uphold quality