Lead Tech, Quality Control

DeSoto, KS, US
March 14 2018
Organization Type
Requisition ID: QUA007100

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Merck Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. 


The Lead Technician, Quality Control  position is available at the Merck Animal Health facility in De Soto, Kansas, located near Kansas City metropolitan area.  The DeSoto facility is expanding operations to manufacturing vaccines and biologics for large and companion animals.  Leveraging an experienced and innovative team environment, the key technologies at the site are biologics production using fermentation and cell culture platforms, filling and packaging.

The primary purpose of this position is to perform advanced laboratory procedures independently for the testing of veterinary biologicals according to strict government and company imposed guidelines. Must be able to evaluate, trouble-shoot, and perform testing activities independently. May be involved in the training of technicians. Development and improvement activities (interdepartmental activities) are more involved and are completed independently.

  • Independently plan and perform quality control procedures. Review records for compliance. This position requires a thorough understanding of the principles underlying the testing procedures used in the areas of assignment. In addition, a thorough understanding of the material being evaluated (i.e. virus, bacteria, cell line) is also required. The ability to use experience and/or education to optimize testing activities is expected. 
  • Troubleshooting established testing methods and evaluating new testing methods. Maintain and evaluate the sequential analysis of the testing standards used in the area of assignment. Prepare and qualify test reagents/supplies. Create and revise Standard Operating Procedures (SOPs)/test methods/test worksheets for testing performed in the area(s) of assignment. 
  • Enter test results in the appropriate tracking system. Cross-check wet records with information in the tracking system and evaluate test dispositions (satisfactory, unsatisfactory, inconclusive, no test). Report all unusual, non-routine occurrences when performing tasks to Quality Control (QC) Manager. This includes completing the necessary documentation.
  • Participate in project teams and/or complete/design special projects. 
  • Participate in other special projects or activities as assigned by management.




  • Minimum Bachelors degree in a related field

  • A minimum of five years related experience including a thorough knowledge of procedures, paperwork, and specific laboratory testing experience.  
  • Ability to work independently and follow oral and written instructions.
  • Good oral and written communication skills.  
  • Ability to work on a team with people from both inside Quality Control as well as other departments such as Research and Development and Manufacturing. 
  • Excellent mathematics and writing skills.

  • Proficiency with advanced laboratory techniques and procedures relating to 9 CFR testing of veterinary biologicals preferred
  • Viral Titration, ELISA and gel electrophoresis experience preferred
  •  Effective leadership skills.
  • Ability to independently prepare written reports for submission to United States Department of Agriculture (USDA) and other agencies

Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. 


If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com.


Search Firm Representatives Please Read Carefully: 

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.


Visa sponsorship is not available for this position.


For more information about personal rights under Equal Employment Opportunity, visit:


            EEOC Poster

            EEOC GINA Supplement 


Job: Quality Lab Related
Other Locations:
Employee Status: Regular
Travel: Yes, 5 % of the Time
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name: Merck

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