Quality Control Process Inspector I

ZEISS Group•Ontario, CA

1d•Onsite

About The Position

The QC Process Inspector supports Quality Assurance and Quality Control activities in compliance with FDA Quality System Regulations and ISO 13485 standards. This role is responsible for performing in-process quality audits throughout the manufacturing of intraocular lenses (IOLs) to ensure products meet established specifications and quality requirements. This position plays a key role in monitoring manufacturing processes, identifying quality concerns, analyzing data, and supporting corrective actions related to machining, tumbling, cleanroom, and packaging operations. The ideal candidate is detail-oriented, quality-focused, and able to work effectively in a collaborative manufacturing environment.

Requirements

High School Diploma or equivalent required
1–3 years of Quality Control inspection experience in a regulated industry
Basic computer proficiency, including Microsoft Office (Outlook, Word, Excel)
Strong communication and documentation skills with high attention to detail
Ability to read, understand, and follow instructions, procedures, and written communication
English required
Basic math skills, including working with fractions, decimals, and measurements
Strong problem-solving and decision-making abilities with a common-sense approach
Self-motivated, energetic team player who can work independently with minimal supervision

Nice To Haves

Associate degree preferred
bilingual skills are a plus

Responsibilities

Monitor daily operations to ensure compliance with established procedures, specifications, and work order instructions
Perform in-process audits for machining, tumbling, cleanroom, and packaging operations according to approved procedures
Identify and report unusual quality conditions or process deviations to Quality Management
Initiate NCRs (Non-Conformance Reports) for non-conforming products, out-of-specification processes, and process failures
Assist Operations Group Leaders and Machine Operators with in-process inspections, corrective actions, and compliance activities
Verify equipment calibration according to established procedures and schedules
Ensure compliance with company safety policies, GMP, and GDP requirements
Document inspection findings, maintain accurate records, and communicate results to the Quality Control Supervisor
Support the development and implementation of quality control procedures and continuous improvement initiatives
Collaborate with production teams to identify and resolve quality issues in a timely manner
Participate in internal audits and support external inspections as needed
Maintain a clean, organized, and compliant work environment
Stay current on industry standards, FDA regulations, and best practices related to medical device quality control