Precision QC Inspector: Pharma/Medical Device Standards

Energy Jobline ZR; Camarillo (CA); On-site; USD 55,000 - 75,000; Full time

Job summary

Energy Jobline ZR seeks a Quality Control Inspector to test and inspect materials, parts, and products across production stages. Impeccable documentation and collaboration on improvements are required, especially in pharma/medical device contexts.

Responsibilities include NCR initiation, GDP-compliant documentation, raw material decisions, and gamma irradiation-related inspections. Strong communication and precise measurement skills are essential in this ISO cleanroom setting.

Qualifications

• Minimum 3 years of experience in manufacturing quality control inspections.
• At least 1 year of experience handling technical documentation and corrective actions in a pharmaceutical or medical device setting.
• Working knowledge of ISO 9001, ISO 13485, and 21 CFR Parts 210, 211, or 820.
• Proven ability to execute strict GMP operations by following detailed SOPs.
• Hands-on experience using precision measuring devices such as calipers, rulers, tape measures, and pin gauges.

Responsibilities

• Perform incoming, first article, in-process, and final inspections to ensure full compliance with standards.
• Initiate nonconformance reports (NCR) for non-conforming materials identified during operations.
• Review, complete, and release manufacturing job order documents using GDP.
• Approve or reject raw materials based on established quality standards and communicate findings to required parties.
• Support cross-functional investigations into non-conformance findings and provide recommendations for improvements.
• Maintain a safe, orderly workspace and wear PPE in an ISO cleanroom environment.

Skills

Interpersonal skills

Communication skills

Mathematics

Computer literacy

ERP systems

Education

High School Diploma or equivalent

Tools

Calipers

Rulers

Tape measures

Pin gauges

SyteLine ERP

Job description

Energy Jobline ZR seeks a Quality Control Inspector to test and inspect materials, parts, and products across production stages. Impeccable documentation and collaboration on improvements are required, especially in pharma/medical device contexts.

Responsibilities include NCR initiation, GDP-compliant documentation, raw material decisions, and gamma irradiation-related inspections. Strong communication and precise measurement skills are essential in this ISO cleanroom setting.