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Open Position

Quality Control Manager, Noble Pharma, LLC

Quality Assurance
Menomonie, WI


Position Description

As Quality Control (QC) Manager, the incumbent will be responsible for successfully providing technical and analytical leadership to the QC function including microbiology labs. The person will be responsible for overseeing the lab instrumentation qualification and operation as well as coordinating the analytical test method transfers and validations. The individual will be responsible for the execution and administration of the GXP Quality System pertaining to QC as well as for managing lab investigations/deviations. The individual should be willing to participate hands-on in writing procedures as well as in conducting testing. Experience with HPLC/UPLC and in working in a GMP/regulated laboratory environment is preferred. 

Essential Duties & Responsibilities
Key responsibilities will include
  • Maintaining QC function in compliance with applicable GXP regulations.
  • Delivering QC operational performance and providing a timely assessment of any gaps in labs capability. 
  • Oversee the qualification and operating procedure creation for various lab equipment 
  • Provide support for maintaining training files for employees to ensure compliance with applicable regulations 
  • Ensure that all quality trends are evaluated, that root causes are identified, and corrective actions are implemented. 
  • Ensure that the receipt, control, sampling, inspections, testing, and disposition status for all raw materials and associated components upon transfer from distribution or other authority comply with regulatory requirements 
  • Participate in analytical method development for HPLC/UPLC based methods
  • Participate in the customer complaints reviews, change controls assessments, deviation investigations, and resulting CAPAs
  • Oversee the finished product retain system 
  • Escalate properly to Senior Management of potential or real situations that require management addressing. 
  • Stay abreast of evolving regulatory compliance practices related to GMP and GLP systems. 
  • Other duties as assigned 

Regularly interacts with other key functions, senior leadership and external clients.

Establish and maintain an environment that stresses and encourages teamwork.

Qualification & Experience
  • Bachelor’s degree in Science or Engineering; graduate degree preferred 
  • Strong problem-solving skills & excellent oral and written communication skills 
  • Strong ability to motivate QC team
  • Experience in either the pharmaceutical industry, or lab operations environment 
  • Preferred Proficiencies: MS Visio, MS Project, MS Excel, MS Power Point, MS Word, or similar software platforms  

Application for
Quality Control Manager, Noble Pharma, LLC

Vets Plus, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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