Quality Engineer

Zeiss Group in; Chesterfield (MO); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical

Vision

Dental

401k Matching

Employee Assistance

Vacation pay

Sick pay

Job summary

ZEISS in Chesterfield, MO seeks a Quality Engineer to oversee QA, validations and documentation, ensuring compliance with industry standards and regulatory requirements across manufacturing.

Lead QA protocols, audits and CAPA using Six Sigma/Lean; drive continuous improvement from design through final inspection. Requires engineering/quality degree and 2–5 years in manufacturing QA; strong communication skills.

Qualifications

• A bachelor's degree in engineering, quality management, or related field.
• 2–5 years of experience in quality assurance and validation in manufacturing.
• ASQ Certified Quality Engineer is preferred.
• Proficiency in QA methodologies, validations and root cause analysis.
• Understanding of ISO 9001, 13485 and 14001.
• Excellent verbal and written communication skills.

Responsibilities

• Develop and maintain QA protocols aligned with standards.
• Review quality metrics to assess process effectiveness.
• Collaborate with cross-functional teams to integrate quality from design to final inspection.
• Ensure ISO compliance and prepare for external audits.
• Document QA activities and maintain SOPs.
• Lead root cause analyses and CAPA actions.

Skills

Quality assurance

Validation management

Root cause analysis

ISO standards

Communication skills

Education

Bachelor's degree in engineering or quality management

Job description

How many companies can say they have been in business for over 178 years?!

Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the ever-changing environments in a fast-paced world, meeting it with cutting edge 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!

Location:

Chesterfield, MO

What's the role?

The Quality Engineer is responsible for overseeing the quality assurance processes, validations and documentation to ensure compliance with industry standards and regulatory requirements. This role involves managing quality assurance procedures, conducting validations, and implementing continuous improvement initiatives to maintain high-quality standards in manufacturing operations.

Here's what you'll do:

Quality Assurance

• Develop, implement, and maintain comprehensive quality assurance protocols and procedures that align with industry best practices and regulatory requirements.
• Conduct regular reviews of quality metrics and performance indicators to assess the effectiveness of quality assurance processes.
• Collaborate with cross-functional teams to ensure that quality standards are integrated into all stages of production, from design to final inspection.

Quality Engineer (Finance)

About Us:

Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the ever-changing environments in a fast-paced world, meeting it with cutting edge 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!

Location:

Chesterfield, MO

What’s the role?

The Quality Engineer is responsible for overseeing the quality assurance processes, validations and documentation to ensure compliance with industry standards and regulatory requirements. This role involves managing quality assurance procedures, conducting validations, and implementing continuous improvement initiatives to maintain high-quality standards in manufacturing operations.

Sound Interesting?

Here’s what you’ll do:

Quality Assurance

• Develop, implement, and maintain comprehensive quality assurance protocols and procedures that align with industry best practices and regulatory requirements.
• Conduct regular reviews of quality metrics and performance indicators to assess the effectiveness of quality assurance processes.
• Collaborate with cross-functional teams to ensure that quality standards are integrated into all stages of production, from design to final inspection.

Regulatory Compliance

• Ensure that all quality assurance processes comply with relevant ISO standards, including ISO 9001 (Quality Management Systems), ISO 13485 (Medical Devices), and ISO 14001 (Environmental Management).
• Stay updated on changes to regulatory requirements and industry standards and implement necessary adjustments to quality assurance practices.
• Prepare for and facilitate external audits by regulatory bodies, ensuring that all documentation and processes are in compliance.

Process Improvement

• Identify areas for improvement in manufacturing processes through data analysis, process mapping, and stakeholder feedback.
• Lead continuous improvement initiatives, utilizing methodologies such as Six Sigma, Lean Manufacturing, or Kaizen to enhance product quality and operational efficiency.
• Monitor the effectiveness of implemented improvements and adjust strategies as needed to achieve desired outcomes.

Audits and Inspections

• Conduct internal audits of quality assurance processes, production practices, and calibration records to ensure compliance with established standards.
• Prepare detailed audit reports outlining findings, recommendations, and corrective actions, and follow up to ensure timely resolution of identified issues.
• Participate in external audits and inspections, providing necessary documentation and support to demonstrate compliance with quality standards.

Documentation

• Maintain accurate and up-to-date records of quality assurance processes, validation activities, audit findings, and corrective actions.
• Develop and update standard operating procedures (SOPs) related to quality assurance and validation, ensuring that all documentation is accessible and compliant with regulatory requirements.
• Ensure that all quality-related documentation is properly archived and retrievable for audits and inspections.

Root Cause Analysis

• Lead investigations into quality issues, utilizing root cause analysis techniques such as the 5 Whys, Fishbone Diagram, or Failure Mode and Effects Analysis (FMEA).
• Develop and implement corrective and preventive actions (CAPA) based on investigation findings to address quality concerns and prevent future occurrences.
• Monitor the effectiveness of CAPA initiatives and report on progress to management and relevant stakeholders.
• Other duties assigned by management

Do you qualify?

• A bachelor's degree in engineering, quality management, or a related field is required.
• 2-5 year of experience in quality assurance and validation management in a manufacturing environment.
• Certification in quality management (e.g., ASQ Certified Quality Engineer) is preferred.
• Proficiency in quality assurance methodologies, equipment validations and root cause analysis.
• Comprehensive understanding of ISO standards, including ISO 9001, ISO 13485, and ISO 14001.
• Excellent verbal and written communication skills, with the ability to train and guide production staff.

Work Environment:

• The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• The noise level in the work environment is usually moderate.
• This job description does not state nor imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job related duties as requested by management and will also be required to meet safety-related requirements. All requirements are subject to possible modification to reasonably accommodate individuals with a disability.

Position Type/Expected Hours of Work

• This is a full-time position. Hours of work are generally Monday through Friday, 40 hours per week.

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: Jo Anne Mittelman

Zeiss 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).