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Quality Documentation Specialist
Job in
Tonganoxie, Leavenworth County, Kansas, 66086, USA
Listed on 2026-08-06
Listing for:
Colgate-Palmolive Company
Full Time
position Listed on 2026-08-06
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Food Quality & Safety
Job Description & How to Apply Below
Job Description
A part of Colgate-Palmolive since 1976, Hill's Pet Nutrition offers the highest-quality pet nutrition available through product lines Prescription Diet and Science Diet. Veterinarians worldwide recommend and feed their own pets Hill's products more than any other brand of pet food.
Available in approximately 80 countries around the world, our extensive line of products includes more than 60 Prescription Diet brand pet foods and more than 50 Science Diet brand pet foods.
We believe all animals should be loved and cared for during their lifetimes. That is why we are proud our pet foods can make a difference in your pet's life.
A career at Hill's Pet Nutrition or Colgate-Palmolive is an excellent opportunity if you seek a global experience, constant challenge, and development opportunities in an environment that respects work/life effectiveness.
Information at a Glance
Apply now
Job Title:
Quality Documentation Specialist
Travel Required?:
Travel - up to 10% of time
Posting
Start Date:
8/3/26
On-site
No Relocation Assistance Offered
Job Number #175293 - Tonganoxie, Kansas, United States
Who We Are
Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name!
Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values-Caring, Inclusive, and Courageous-we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all.
Role Summary The Quality Documentation Specialist maintains and elevates the site's Quality Management System (ETQ) in full compliance with regulatory requirements and Colgate Quality Standards. Reporting to the Associate Manager, Quality Compliance, this role serves as a technical resource driving continuous improvement, key quality systems execution, and effective Management of Change (MOC) life cycles. By maintaining audit readiness and site-wide compliance, this position directly impacts overall product quality and operational excellence across the manufacturing site.
Responsibilities
* Oversee and optimize site document control, record management, and Management of Change (MOC) systems to support compliance with cGMP, FSMA, and Colgate Quality Standards.
* Monitor and review daily, weekly, and monthly production records across physical and electronic data capture systems (MES/OPERA) to ensure complete audit readiness and timely finished product release.
* Track, analyze, and report site Quality KPIs-including product non-conformances, holds, customer complaints, and training compliance-to drive data-driven continuous improvement.
* Partner cross-functionally with site leadership, plant teams, and regulatory bodies to resolve technical compliance issues and support internal/external quality audits.
* Develop and deliver quality compliance training modules in collaboration with leadership to build site-wide technical proficiency and safety standards.
Required Qualifications
* Bachelor's degree
* 1+ years of experience in a manufacturing environment
* 1+ years of experience working with quality systems and Good Documentation Practices (cGMP)
* Demonstrated proficiency with enterprise document management systems and software (e.g., SAP, Google suite)
* Ability to lift up to 50 lbs and work flexible shifts (nights, weekends, holidays) to support operational needs
Preferred Qualifications
* Bachelor's degree in Food Science, Engineering, Chemistry, Biology, Microbiology, or a related technical field
* 1+ years of quality experience specifically within a food or CPG manufacturing environment
* Active certifications such as PCQI, HACCP, or Certified Auditor
* Direct experience with regulatory and auditing bodies (e.g., FDA, USDA, SQF, AIB)
* Proficiency with statistical process control tools (e.g., SPC, Minitab)
Compensation and Benefits
Salary Range $52,800.00 - $80,000.00 USD
Pay is determined based on experience, qualifications, and location. Salaried employees may also be eligible for discretionary bonuses, profit-sharing, and long-term incentives for Executive-level roles.
Benefits:
Salaried employees enjoy a comprehensive benefits package, including medical, dental, vision, basic life insurance, paid parental leave, disability coverage, and participation in the 401(k) retirement plan with company matching contributions subject to eligibility requirements. Additional benefits include a minimum of 15 vacation/PTO days (hourly employees receive a minimum of 120 hours) and 13 paid holidays (vacation days are prorated based on the employee's hire date within the calendar year).
Paid sick leave is adjusted based on role and location in accordance with local laws. Detailed information regarding paid sick leave entitlements will be provided to…
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