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QC Scientist II

Thermo Fisher Scientific

QC Scientist II

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals. 

 

Location/Division Specific Information 

St. Louis, MO 

 

How will you make an impact? 

As a QC Scientist II, you will do important work that makes a real-world impact. Your efforts will help in finding cures for cancer, protecting the environment, and ensuring food safety. You will be supported in achieving your career goals. 

 

What will you do?  

  • Create QC Raw Materials (QCRM) specification documents in accordance with internal SOPs and external regulations. 

  • Review batch records, process validation protocols/reports, technical transfer documents, and product specifications with high attention to detail and assess the impact of changes on the testing laboratory 

  • Collaborate with QCM laboratory scientists to support laboratory needs and questions. 

  • Review bioburden and endotoxin Raw Data for the QC Microbiology (QCM) laboratory 

  • Generate Certificates of Testing for bioburden and endotoxin results 

  • Support QCM testing by providing matrices, SOPs, and other testing protocols  

 

How will you get here? 

Education 

BS/BA in biology, biochemistry, chemistry, or a related science field, or a four-year degree with meaningful experience. 

Experience 

  • Minimum of two (2) years of experience in cGMP or another highly regulated industry. 

  • Experience with bioburden and/or endotoxin assays 

 

Knowledge, Skills, Abilities 

  • Knowledge of cGMP regulations and international health authority guidelines. 

  • Knowledge of compendial requirements for raw material testing is desired 

  • Proficient in Microsoft Office (Word and Excel). 

  • Experience with Smartsheet and Trackwise systems is desired 

 

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals. 

 

Locations

  • St. Louis, Missouri, United States of America

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • cGMP regulations knowledgeintermediate
  • Bioburden and endotoxin assaysintermediate
  • Microsoft Office proficiencyintermediate
  • Smartsheet and Trackwise (desired)intermediate
  • Compendial raw material testingintermediate

Required Qualifications

  • BS/BA in biology, biochemistry, chemistry, or related science field (experience)
  • Minimum 2 years experience in cGMP or regulated industry (experience)
  • Experience with bioburden and/or endotoxin assays (experience)

Responsibilities

  • Create QC Raw Materials specification documents
  • Review batch records, validation protocols, and specifications
  • Collaborate with QCM laboratory scientists
  • Review bioburden and endotoxin raw data
  • Generate Certificates of Testing
  • Support QCM testing with matrices and SOPs

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Thermo Fisher Scientific logo

QC Scientist II

Thermo Fisher Scientific

QC Scientist II

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals. 

 

Location/Division Specific Information 

St. Louis, MO 

 

How will you make an impact? 

As a QC Scientist II, you will do important work that makes a real-world impact. Your efforts will help in finding cures for cancer, protecting the environment, and ensuring food safety. You will be supported in achieving your career goals. 

 

What will you do?  

  • Create QC Raw Materials (QCRM) specification documents in accordance with internal SOPs and external regulations. 

  • Review batch records, process validation protocols/reports, technical transfer documents, and product specifications with high attention to detail and assess the impact of changes on the testing laboratory 

  • Collaborate with QCM laboratory scientists to support laboratory needs and questions. 

  • Review bioburden and endotoxin Raw Data for the QC Microbiology (QCM) laboratory 

  • Generate Certificates of Testing for bioburden and endotoxin results 

  • Support QCM testing by providing matrices, SOPs, and other testing protocols  

 

How will you get here? 

Education 

BS/BA in biology, biochemistry, chemistry, or a related science field, or a four-year degree with meaningful experience. 

Experience 

  • Minimum of two (2) years of experience in cGMP or another highly regulated industry. 

  • Experience with bioburden and/or endotoxin assays 

 

Knowledge, Skills, Abilities 

  • Knowledge of cGMP regulations and international health authority guidelines. 

  • Knowledge of compendial requirements for raw material testing is desired 

  • Proficient in Microsoft Office (Word and Excel). 

  • Experience with Smartsheet and Trackwise systems is desired 

 

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals. 

 

Locations

  • St. Louis, Missouri, United States of America

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • cGMP regulations knowledgeintermediate
  • Bioburden and endotoxin assaysintermediate
  • Microsoft Office proficiencyintermediate
  • Smartsheet and Trackwise (desired)intermediate
  • Compendial raw material testingintermediate

Required Qualifications

  • BS/BA in biology, biochemistry, chemistry, or related science field (experience)
  • Minimum 2 years experience in cGMP or regulated industry (experience)
  • Experience with bioburden and/or endotoxin assays (experience)

Responsibilities

  • Create QC Raw Materials specification documents
  • Review batch records, validation protocols, and specifications
  • Collaborate with QCM laboratory scientists
  • Review bioburden and endotoxin raw data
  • Generate Certificates of Testing
  • Support QCM testing with matrices and SOPs

Target Your Resume for "QC Scientist II" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for QC Scientist II. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "QC Scientist II" , Thermo Fisher Scientific

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for QC Scientist II @ Thermo Fisher Scientific.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.