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Associate Quality Control Analyst

Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.  


Celerion has a full-time opening for an Associate Quality Control Analyst in our Bioanalytical Division in Lincoln, NE.


This is an excellent opportunity to help ensure all Bioanalytical data is correct and complete. This is an office-based administrative role working Monday - Friday between the hours of 8am-5pm. We are only considering local candidates for this role.


Responsibilities:
  • Verify Excel spreadsheets and calculations
  • Assist in paperwork routing, document assembly, and verification of information packet completeness
  • Verify raw data against information in Methods or Standard Operating Procedures:
  • Ensure Compliance with general SOP requirements
  • Verify Solution composition or concentration, including calculations used to determine the concentrations are correct
  • Verify volumes used and any processing step documented are as explained in the sample processing procedures


Requirements:
  • Associate Degree in Chemistry, Biology or related science and 6 months of related experience OR Bachelor’s degree in Chemistry, Biology, or related science.
  • Exceptional attention to detail and proofreading ability are required.
  • Excellent time management skills and proficiency with Microsoft Office are required.


Celerion Values:       Integrity   Trust   Teamwork   Respect


Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

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Average salary estimate

$50000 / YEARLY (est.)
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$45000K
$55000K

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Celerion’s focus is on the implementation of innovative strategies to generate key data very early to enable go/no-go decisions in drug development. With a large clinical capacity of more than 600 beds , efficient bioanalytical laboratories and ex...

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Full-time, onsite
DATE POSTED
June 17, 2025

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