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ISOGMP Coordinator North America

DeLaval

Job Location:

Kansas City, MO - USA

Monthly Salary: Not provided by the employer

Posted: 11 October 2026 (15 days ago)

Application Deadline: 8 January 2027

Vacancies: 1 Vacancy

Job Summary

Job Location: Kansas City

Title: ISO/GMP QMS Coordinator North America

Company: DeLaval

Location: Onsite in Kansas City MO

At DeLaval we have been driving progress in milk production for more than 140 years by developing innovative solutions for dairy producers worldwide. Working with our dealer network across North America we provide integrated milking systems consumables and services that help dairy producers improve animal welfare food safety profitability and operational efficiency.

We are seeking an experienced ISO/GMP QMS Coordinator to lead and maintain our Quality Management System (QMS) across North America. This role is responsible for ensuring compliance with ISO 9001 GMP/FDA 21 CFR Part 211 requirements and other applicable standards while driving continuous improvement operational excellence and customer satisfaction.

In Support of Our Amazing Team We Offer

Competitive compensation
Year-end bonus
Paid vacation plus additional time off at the end of the year
401(k) with company match
Medical Dental and Vision benefits
Work-life balance
Professional development opportunities
And MORE!

About DeLaval

DeLaval is a leading global supplier of solutions that improve the performance of farms for professional food producers. We support our customers in reducing their environmental footprint while improving food production profitability and the well-being of the people and animals involved.

Our solutions are used by millions of dairy farmers around the globe every day. At DeLaval we prioritize our people and their safety. We pride ourselves on our culture of thinking and acting as One DeLaval. We empower our people to Make Things Happen and encourage Setting Direction.

Learn more about DeLaval at:

Key Responsibilities

Own maintain and continuously improve the Quality Management System (QMS) ensuring compliance with ISO 9001 GMP/FDA 21 CFR Part 211 and other applicable standards.
Lead internal audits coordinate external audits and ensure ongoing certification readiness across multiple facilities.
Develop implement and maintain Standard Operating Procedures (SOPs) to standardize processes and support regulatory compliance.
Monitor and analyze quality and process performance data to identify trends risks and opportunities for improvement.
Lead root cause investigations and implement Corrective and Preventive Actions (CAPA) to address nonconformities and prevent recurrence.
Provide training and coaching to employees at all levels on quality systems regulatory requirements and best practices.
Manage ISO 9001 and GMP/FDA certification activities from preparation through successful audit completion.
Partner with Operations Engineering Supply Chain Production and other departments to integrate quality requirements into business processes.
Ensure compliance with safety environmental and regulatory requirements during all quality-related activities.
Support production teams by providing guidance on quality standards procedures and continuous improvement initiatives.
Maintain quality records documentation and reporting systems to support regulatory and customer requirements.
Lead and support continuous improvement projects focused on quality efficiency and customer satisfaction.
Promote a culture of quality accountability and operational excellence throughout the organization.
Ensure the organization remains current with evolving regulatory and industry requirements.

Requirements

Bachelors degree in Engineering Business Science or a related field required.
Minimum of 7-10 years of experience in quality management quality systems or regulatory compliance roles.
Strong working knowledge of ISO 9001 Quality Management Systems and GMP/FDA 21 CFR Part 211 requirements.
Experience leading internal and external audits certification activities and regulatory inspections.
Proficiency with quality management tools and methodologies such as FMEA SPC 8D CAPA root cause analysis and risk management.
Strong leadership skills with the ability to influence motivate and drive change across cross-functional teams.
Excellent written and verbal communication skills including experience developing procedures training materials and management reports.
Demonstrated success leading continuous improvement and operational excellence initiatives.
Strong analytical and problem-solving skills with exceptional attention to detail.
Ability to manage multiple priorities and work effectively in a fast-paced environment.
Ability and willingness to travel as needed for audits training and multi-site support.

Preferred Qualifications

ISO 9001 Lead Auditor certification
Six Sigma Green Belt or higher certification
Experience supporting multi-site manufacturing or production environments
Knowledge of quality planning process validation and risk-based quality management systems

If you are passionate about quality continuous improvement regulatory compliance and building systems that drive business success we encourage you to apply.

DeLaval is an equal opportunity employer.

Required Experience:

Apply Now