Quality Engineer

About Us:

How many companies can say they’ve been in business for over 177 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?  

SUMMARY

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:

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following:

(Responsibilities that are central to the job and MUST be performed either unaided, or with the assistance of a reasonable accommodation, ref.

ADA)

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 ...