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Specialist/Sr. Specialist Quality Contract Manufacturing

Colgate-Palmolive

Topeka, KS

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JOB DETAILS
SALARY
$97,000–$125,000 Per Year
SKILLS
Animal Nutrition, Auditing, Biology, Chemistry, Continuous Improvement, Contract Management, Contract Manufacturing, Corporate Policies, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Diversity, Documentation, FDA Requirements, Food Safety, Food Science, Home Care, Internal Audit, Leadership, Maintain Compliance, Manufacturing, Microbiology, Operational Support, People Management, Performance Metrics, Personal Care, Product Data Management (PDM), Purchasing/Procurement, Quality Assurance, Quality Management, Quality Metrics, Regulations, Regulatory Compliance, Regulatory Requirements, Risk Analysis, Skin Care, Talent Management, Vendor/Supplier Evaluation, Vendor/Supplier Management
LOCATION
Topeka, KS
POSTED
15 days ago
No Relocation Assistance Offered

Job Number #172287 - Topeka, 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.


The Specialist/Sr. Specialist Quality Contract Manufacturing is part of the global program for contract manufacturing and Quality Standards implementation. Focus includes but it is not limited to the following areas:


+ Coordinate the North American Contract Manufacturing (CM) quality program

+ Support CM operations to incorporate and comply with Global CM Quality Standards

+ Work with S&T to ensure the CM specifications for finished goods and raw materials are updated and in

+ compliance with applicable regulation and the Global CM Quality Standards

+ Drive CMs to action continuous improvement activities

+ Manages and coordinates the execution of the Enhanced Supplier Management program for North

+ America (NA) CMs

+ Supports the Quality representative for the CM Technology Transfer process

+ Support Quality Compliance initiatives as required (Quality standards implementation and auditing

+ programs, etc.)


Responsibilities


+ Manage the NA region CMs to ensure adherence to Global CM Quality Standards, applicable FSMA

+ regulations, completion and distribution of the site annual management reports, drive continuous

+ improvement, and Quality Technical Agreements.

+ Manages the NA region customer complaint investigations. Ensures proper documentation, CAPA, MoC and failure investigations (including microbiological incidents). Manages and reports KPI results (Non-conformance, consumer complaints, FG release time, Coman mock recalls, etc.).

+ For the NA region, assures acceptable KRSs are reviewed and approved prior to releasing product from the contract manufacturer’s control, as defined and required on Hill’s specifications and regulatory requirements.

+ Ensure all product non-conformances are properly investigated, documented and approved by Corporate Quality prior to product release

+ Drives completion of the annual CM risk assessments and coordinates the execution of the audit program in NA.

+ Ensure that ESM KPIs are met and reported to leadership. Provide guidance to maintain CM's audit readiness.

+ Participate in the Global Compliance Program, supporting Quality Standards Implementation follow up,participate in the auditing programs (internal audits, supplier audits, corporate audits, FSMA readiness,etc.)

+ Ensure that I&S have all CM formulas and specifications updated in the PDM system.

+ Ensure the NetOps/Procurement/CS&L formally communicates to the CM the updated formulas and specifications.


Required Qualifications


+ Bachelor's degree in Food Science, Biology, Chemistry, Engineering or other related field

+ 4+ years manufacturing experience in a Food or drug/ cGMP environment

+ 3+ years experience in Quality related field

+ Working knowledge of FDA regulations, Food Safety, or cGMPs


Preferred qualifications


+ Masters of Food Science, Biology, Chemistry, Engineering or other related field

+ Certification in PCQI, SQF Practitioner, BPCS

+ Certified Auditor

+ Familiar with EU/Brazil/Japan/China food regulations


Compensation and Benefits

Salary Range $97,000.00 - $125,000.00 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 employees upon hiring and may be subject to adjustments based on changes in legislation or company policies.


Our Commitment to Inclusion

Our journey begins with our people—developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self, is treated with respect, and is empowered by leadership to contribute meaningfully to our business.


Equal Opportunity Employer

Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law.


Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form (https://docs.google.com/forms/d/e/1FAIpQLSdaxk_eF4utznQoVHlxmL9jVFJbOkM4Oe5CAdKOg-h9EPdLfg/viewform) should you require accommodation.


For additional Colgate terms and conditions, please click here (https://www.colgatepalmolive.com/content/dam/cp-sites/corporate/corporate/en_us/corp/locale-assets/pdf/colgate-terms-and-conditions-2023.pdf) .


#LI-Hybrid

About the Company

C

Colgate-Palmolive

The small soap and candle business that William Colgate began in New York City early in the 19th century is now, more than 200 years later, a truly global company serving hundreds of millions of consumers worldwide. Throughout this history, Colgate people and Colgate values have been at the heart of our success. Today, Colgate focuses on four core businesses Oral Care, Personal Care, Home Care and Pet Nutrition. Colgate now sells its products in over 200 countries and territories worldwide.
COMPANY SIZE
10,000 employees or more
INDUSTRY
Consumer Packaged Goods Manufacturing
WEBSITE
https://www.colgatepalmolive.com/en-us