QA Validation Engineer
Lenexa, KS · On-site
Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry OR * Master ...
QA Validation Engineer
Lenexa, KS · On-site
Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry OR * Master ...
Validation Engineer
North Haven, CT · On-site
... Clinical trials of drugs, biologics and medical devices. * We have a few immediate job ... As a Validation Engineer within the Mold & Capital Tooling Organization, you'll play a pivotal role ...
Validation Engineer
North Haven, CT · On-site
... Clinical trials of drugs, biologics and medical devices. * We have a few immediate job ... As a Validation Engineer within the Mold & Capital Tooling Organization, you'll play a pivotal role ...
Validation Engineer
Los Angeles, CA · On-site
$90K - $110K/yr
... biologics, and medical devices. For more information, please visit our website at eliquent.com. We are seeking a highly skilled Commissioning, Qualification, and Validation (CQV) Engineer to join our ...
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Validation Engineer
Los Angeles, CA · On-site
$90K - $110K/yr
... biologics, and medical devices. For more information, please visit our website at eliquent.com. We are seeking a highly skilled Commissioning, Qualification, and Validation (CQV) Engineer to join our ...
Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The ValidationEngineer will ...
Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The ValidationEngineer will ...
Validation Engineer IV
Rockville, MD · On-site
Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The ValidationEngineer will ...
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Validation Engineer IV
Rockville, MD · On-site
Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The ValidationEngineer will ...
... biologics manufacturing as part of a fast-paced and collaborative global validation team ... Validation Engineer III - 7+ years * Understanding of industry standards and best practices for a ...
... biologics manufacturing as part of a fast-paced and collaborative global validation team ... Validation Engineer III - 7+ years * Understanding of industry standards and best practices for a ...
... biologics manufacturing as part of a fast-paced and collaborative global validation team ... Validation Engineer III - 7+ years * Understanding of industry standards and best practices for a ...
... biologics manufacturing as part of a fast-paced and collaborative global validation team ... Validation Engineer III - 7+ years * Understanding of industry standards and best practices for a ...
Validation Engineer II
Rockville, MD · On-site
Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The ValidationEngineer will ...
Quick apply
Validation Engineer II
Rockville, MD · On-site
Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The ValidationEngineer will ...
... biologics manufacturing as part of a fast-paced and collaborative global validation team ... Validation Engineer III - 7+ years * Understanding of industry standards and best practices for a ...
... biologics manufacturing as part of a fast-paced and collaborative global validation team ... Validation Engineer III - 7+ years * Understanding of industry standards and best practices for a ...
... biologics manufacturing as part of a fast-paced and collaborative global validation team ... Validation Engineer III - 7+ years * Understanding of industry standards and best practices for a ...
... biologics manufacturing as part of a fast-paced and collaborative global validation team ... Validation Engineer III - 7+ years * Understanding of industry standards and best practices for a ...
Validation Engineer
Montrose, CA · On-site
$95K - $110K/yr
... biologics, and medical devices. For more information, please visit our website at eliquent.com ... We are seeking a highly skilled Commissioning, Qualification, and Validation (CQV) Engineer to join ...
Quick apply
Validation Engineer
Montrose, CA · On-site
$95K - $110K/yr
... biologics, and medical devices. For more information, please visit our website at eliquent.com ... We are seeking a highly skilled Commissioning, Qualification, and Validation (CQV) Engineer to join ...
Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The ValidationEngineer will ...
Our Validation Engineers will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The ValidationEngineer will ...
The Validation Engineer/Scientist - Technical Services / Manufacturing Science (TS/MS) role is a ... Bachelor's degree in microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical ...
The Validation Engineer/Scientist - Technical Services / Manufacturing Science (TS/MS) role is a ... Bachelor's degree in microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical ...
... biologics, cell therapy, or gene therapy manufacturing environment. * Demonstrated experience leading validation strategy and execution in support of Process Performance Qualification (PPQ ...
... biologics, cell therapy, or gene therapy manufacturing environment. * Demonstrated experience leading validation strategy and execution in support of Process Performance Qualification (PPQ ...
The Validation Engineer/Scientist - Technical Services / Manufacturing Science (TS/MS) role is a ... Bachelor's degree in microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical ...
The Validation Engineer/Scientist - Technical Services / Manufacturing Science (TS/MS) role is a ... Bachelor's degree in microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical ...
Validation Engineer II Location: Redmond, Seattle, WA Shifts: Monday to Friday, 8:00am till 5:00pm ... About Us: this is who we are At Just Evotec Biologic , we believe that curiosity is the spark that ...
Validation Engineer II Location: Redmond, Seattle, WA Shifts: Monday to Friday, 8:00am till 5:00pm ... About Us: this is who we are At Just Evotec Biologic , we believe that curiosity is the spark that ...
Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry OR * Master ...
Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry OR * Master ...
Validation Engineer II Location: Redmond, Seattle, WA Shifts: Monday to Friday, 8:00am till 5:00pm ... About Us: this is who we are At Just Evotec Biologic , we believe that curiosity is the spark that ...
Validation Engineer II Location: Redmond, Seattle, WA Shifts: Monday to Friday, 8:00am till 5:00pm ... About Us: this is who we are At Just Evotec Biologic , we believe that curiosity is the spark that ...
... test biologics/drug product/etc. at client sites. The validation specialist will evaluate the ... Interact with clients and works closely with site manufacturing, engineering, and QA to develop ...
... test biologics/drug product/etc. at client sites. The validation specialist will evaluate the ... Interact with clients and works closely with site manufacturing, engineering, and QA to develop ...
Validation Engineer I
Rockville, MD · On-site
... test biologics/drug product/etc. at client sites. The validation specialist will evaluate the ... Interact with clients and works closely with site manufacturing, engineering, and QA to develop ...
Validation Engineer I
Rockville, MD · On-site
... test biologics/drug product/etc. at client sites. The validation specialist will evaluate the ... Interact with clients and works closely with site manufacturing, engineering, and QA to develop ...
Validation Engineer Biology information
See salary details
$22.60 - $27.64
2% of jobs
$27.64 - $32.69
6% of jobs
$32.69 - $37.74
13% of jobs
$39.32 is the 25th percentile. Wages below this are outliers.
$37.74 - $42.79
13% of jobs
$42.79 - $47.84
11% of jobs
The median wage is $50.36 / hr.
$47.84 - $52.88
12% of jobs
$52.88 - $57.93
9% of jobs
$61.82 is the 75th percentile. Wages above this are outliers.
$57.93 - $62.98
13% of jobs
$62.98 - $68.03
13% of jobs
$68.03 - $73.08
6% of jobs
$73.08 - $78.13
3% of jobs
$22
$51
$78
How much do validation engineer biology jobs pay per hour?
As of Jun 8, 2026, the average hourly pay for validation engineer biology in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.
Full-time
Posted 28 days ago
Job description
QA Validation Engineer
The success of a company depends on the passionate people we partner with.
Together, let's share our talents.
As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.
We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.
Indeed, Our "Together, Beyond Animal Health" vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.
As part of our "Diversity, Equity and Inclusion" policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.
Yourmissions :
Location: Lenexa, KS
Job Summary and Purpose
The QA Validation Engineer in Lenexa, KS leads, designs, performs, and reports validation activities on processes, equipment, and systems used in the manufacture of regulated veterinary vaccines for domestic and international markets.
Responsibilities and Key Duties
This job description is intended to convey information essential to understanding the scope, general nature, and level of work performed by job holders. It is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities, or working conditions, nor does it constitute an employment contract. Ceva reserves the right to modify job duties and/or job descriptions at any time to meet business needs.
*VEVRAA Federal Contractor
**Ceva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.
669B
Yourprofile :
Education - Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation work experience in biotech, biological, pharmaceutical or other GMP-regulated industry
OR
Master's degree in Engineering, Biotechnology, Biology, Microbiology with 2+ years of validation work experience in the biotech, biological, pharmaceutical or other GMP-regulated industry required.
The success of a company depends on the passionate people we partner with.
Together, let's share our talents.
As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.
We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.
Indeed, Our "Together, Beyond Animal Health" vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.
As part of our "Diversity, Equity and Inclusion" policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.
Yourmissions :
Location: Lenexa, KS
Job Summary and Purpose
The QA Validation Engineer in Lenexa, KS leads, designs, performs, and reports validation activities on processes, equipment, and systems used in the manufacture of regulated veterinary vaccines for domestic and international markets.
Responsibilities and Key Duties
- Prepare and execute protocols including Cycle Development, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Engineering Studies (ES), Factory Acceptance Test (FAT), and Site Acceptance Test (SAT).
- Review protocol drafts and resolve conflicts or concerns to achieve management pre-approval. Coordinate qualification execution and all aspects of validation projects with Operations, Engineering, Quality Control, and Quality Assurance.
- Perform or supervise protocol execution and maintain documentation in compliance with current Good Documentation Practices (GDP). Review, analyze, and compile protocol data and write reports for management review and approval.
- Perform and document risk assessments to determine validation strategy and approach. Execute re-qualification (RQ) studies and periodic reviews to ensure equipment, systems, and processes remain in a validated state.
- Support and participate in change control processes for qualified and validated equipment, including refrigerators, freezers, incubators, autoclaves, lyophilizers, bioreactors, fermenters, ovens, ampule filling machines, and related systems. Maintain full understanding of applicable change control procedures.
- Provide input to, review, and approve User Requirements Specifications (URS). Write, review, and edit standard operating procedures (SOPs) to align with validation requirements.
- Provide input to Engineering on the preparation and execution of Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT).
- Research equipment and processes to establish parameters and testing methods that meet validation requirements. Support the development of Validation Plans and Schedules.
- Ensure processes and products comply with all local, state, and federal regulations. Oversee CGMP compliance and establish systems that identify opportunities for improvement and recommend changes to improve process effectiveness and quality.
- Perform all other duties as assigned.
- Ability to perform internal and study audits as a lead and participate in external audits as a member of the audit team
- Knowledge of pharmaceutical development, regulatory requirements, and manufacturing sciences with a global perspective
- Knowledge of quality systems tools with the ability to adapt them to organizational needs and global regulatory requirements (GLP, GCP, GMP)
- Ability to validate Excel file programming according to defined objectives
- Proficiency in the use of data logging equipment and instruments
- Experience performing risk assessments, investigations, CAPAs, and Aseptic Process Simulations (APS or media fills) preferred
- Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry
OR - Master's degree in Engineering, Biotechnology, Biology, or Microbiology with 2+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry
- Ability to read, write legibly, and communicate in English
- Visual inspection capability
- Occasional lifting up to 25 pounds
- Tasks frequently require prolonged mental and visual concentration
- None
This job description is intended to convey information essential to understanding the scope, general nature, and level of work performed by job holders. It is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities, or working conditions, nor does it constitute an employment contract. Ceva reserves the right to modify job duties and/or job descriptions at any time to meet business needs.
*VEVRAA Federal Contractor
**Ceva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.
669B
Yourprofile :
Education - Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation work experience in biotech, biological, pharmaceutical or other GMP-regulated industry
OR
Master's degree in Engineering, Biotechnology, Biology, Microbiology with 2+ years of validation work experience in the biotech, biological, pharmaceutical or other GMP-regulated industry required.