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Sr. Specialist, Quality Control

Job in De Soto, Johnson County, Kansas, 66018, USA
Listing for: Merck
Full Time position
Listed on 2026-07-20
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 106200 - 167200 USD Yearly USD 106200.00 167200.00 YEAR
Job Description & How to Apply Below

Sr. Specialist, Quality Control

Our Animal Health Division is investing $895 million in expanding our manufacturing and research & development facilities in De Soto, Kansas—the state’s largest economic development project to date. As a Sr. Specialist, Quality Control you will be part of a world‑class team at our Center of Excellence in the Animal Health Corridor, contributing directly to the production of veterinary products that improve animal health and welfare globally.

This role combines project leadership/coordination and quality oversight to ensure successful QC laboratory method transfers.

Key Responsibilities
  • Serve as the Project lead for the QC laboratory transfers.
  • Serve as the liaison to the project sponsors, keeping them informed of the status of all project activities and resources.
  • Represent the team at project/tier meetings.
  • Evaluate site‑to‑site process/methods.
  • Resolve any Project Issues in an effective manner.
  • Ensure teams are formed to support the project, and monitor timelines to ensure that each phase is completed on schedule, preventing delays.
  • Coordinate site level activities related to the method transfers.
  • Ensure that deliverables meet quality standards before moving to the next phase.
  • Review/approve required test method information (spec sheets, tests, biomaterials/reagents, release criteria).
  • Review/approve protocols and reports associated with the project.
  • Support completion of Transfer Complexity assessment.
  • Author the Quality Risk Management Plan, and support gap assessments.
  • Coordinate Change Control plans and review/approve related Change Records.
  • Ensure readiness for sample management (sampling plans – transport and handling).
  • Support Regulatory Affairs with Outline of Production/Special Outline updates.
Job Requirements
  • Bachelor’s degree in Biology, Microbiology, Chemistry, Animal Science, Biotechnology, or equivalent experience.
  • 10+ years of progressive experience/roles within quality control in USDA‑regulated animal product facilities.
  • Experience with USDA regulations and inspection processes in manufacturing environments.
  • Relevant practical experience with QC laboratory environments, method transfer, or related quality roles in biologics, vaccines, or similar industries.
  • Experience with qualification of facilities, equipment, instruments, and/or utilities.
  • Knowledge of Good Manufacturing Practices (GMP), quality systems, and regulatory expectations.
  • Strong attention to detail, excellent documentation practices, and ability to maintain audit‑ready records.
  • Effective communication and interpersonal skills; ability to collaborate with cross‑functional teams and external vendors.
  • Proficient with MS Office (Word, Excel, PowerPoint); experience with SAP and electronic quality management systems (Reliance, Veeva) preferred.
Preferred Qualifications
  • Experience leading or supporting method transfers and performing go‑sees.
  • Strong project coordination skills and ability to work with cross‑functional teams.
  • Experience with implementation of LIMS.
  • Excellent written and verbal communication skills.
Physical and Work Environment
  • Primarily office‑based with occasional travel between sites.
  • Ability to travel for site visits/go‑sees as required.
Required Skills
  • Adaptability
  • Good Manufacturing Practices (GMP)
  • Laboratory Information Management System (LIMS)
  • Laboratory Operations
  • Manufacturing
  • Manufacturing Environments
  • Project Coordination
  • Quality Control (QC)
  • Quality Control Management
  • Quality Standards
  • Technical Transfer
  • Testing
  • USDA Regulations
Preferred Skills
  • Laboratory Quality Control
  • Quality Management
  • Quality Management Systems (QMS)
Equal Employment Opportunity

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.

For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit the EEOC resources.

Salary

$ – $

Benefits

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision, health care and other insurance benefits for employee and family, retirement benefits, 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at

Location

US and Puerto Rico residents only.

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