About Us:
How many companies can say they’ve been in business for over 179 years?!
Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology. We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, come join the team!
What’s the role?
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.
Sound Interesting?
Here’s what you’ll do:
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
Do you qualify?
High School Diploma or equivalent required; Associate degree preferred
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; bilingual skills are a plus
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
Position Type/Expected Hours of Work
This is a full-time position. Hours of work are Monday through Friday, 7:00 a.m. to 3:00 p.m., 40 hours per week.
Compensation
Hourly pay range for this position is $21.00 - $26.00.
Actual compensation will depend on factors such as location, experience, education, skills, and role scope
Eligible for performance bonus or sales commissions
We have amazing benefits to support you as an employee at ZEISS!
Medical
Vision
Dental
401k Matching
Employee Assistance Programs
Vacation and sick pay
The list goes on!
The above is intended to describe the general content of and requirements for this job. It is not to be construed as an exhaustive statement of requirements, duties, or responsibilities. The Company reserves the right to interpret, amend, or otherwise modify, in whole or in part, any job description at any time, at its sole discretion.
Your ZEISS Recruiting Team:
Maria KhalilZeiss provides Equal Employment Opportunity without unlawful regard to an Applicants race, color, religion, creed, sex, gender, marital status, age, national origin or ancestry, physical or mental disability, medical condition, military or veteran status, citizen status, sexual orientation, pregnancy (includes childbirth, breastfeeding or related medical condition), genetic predisposition, carrier status, gender expression or identity, including transgender identity, or any other class or characteristic protected by federal, state, or local law of the employee (or the people with whom the employee associates, including relatives and friends).