The Laboratory Systems Validation Specialist position will be responsible for defining validation requirements, developing systems validation documentation, generating and executing test protocols ...
The Laboratory Systems Validation Specialist position will be responsible for defining validation requirements, developing systems validation documentation, generating and executing test protocols ...
Lead Validation Specialist
Mundelein, IL · On-site
$55 - $65/hr
... junior validation specialists. OVERVIEW OF RESPONSIBILITIES * Lead and execute IQ/OQ/PQ activities for facilities, utilities, equipment, control systems, and HVAC * Conduct cGMP audits, gap ...
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Lead Validation Specialist
Mundelein, IL · On-site
$55 - $65/hr
... junior validation specialists. OVERVIEW OF RESPONSIBILITIES * Lead and execute IQ/OQ/PQ activities for facilities, utilities, equipment, control systems, and HVAC * Conduct cGMP audits, gap ...
Lead and mentor a team of Data Validation Specialists, supporting career development, delivering regular feedback, and helping individuals thrive in their role * Manage a team's work allocation ...
Lead and mentor a team of Data Validation Specialists, supporting career development, delivering regular feedback, and helping individuals thrive in their role * Manage a team's work allocation ...
Data Validation Specialist
$20 - $25/hr
Contract Overview TEKsystems is seeking detail-oriented and dependable Data Validation Specialists to support a critical systems migration project. This role is responsible for transferring ...
Data Validation Specialist
$20 - $25/hr
Contract Overview TEKsystems is seeking detail-oriented and dependable Data Validation Specialists to support a critical systems migration project. This role is responsible for transferring ...
Data Validation Specialist
$20 - $25/hr
Contract Overview TEKsystems is seeking detail-oriented and dependable Data Validation Specialists to support a critical systems migration project. This role is responsible for transferring ...
Quick apply
Data Validation Specialist
$20 - $25/hr
Contract Overview TEKsystems is seeking detail-oriented and dependable Data Validation Specialists to support a critical systems migration project. This role is responsible for transferring ...
Manager, Data Validation Specialist (Investment Management)
Salt Lake City, UT · On-site
$100 - $125/hr
Lead and mentor a team of Data Validation Specialists, supporting career development, delivering regular feedback, and helping individuals thrive in their role * Manage a team's work allocation ...
Manager, Data Validation Specialist (Investment Management)
Salt Lake City, UT · On-site
$100 - $125/hr
Lead and mentor a team of Data Validation Specialists, supporting career development, delivering regular feedback, and helping individuals thrive in their role * Manage a team's work allocation ...
Validation Engineer I
Rockville, MD · On-site
Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist ...
Validation Engineer I
Rockville, MD · On-site
Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist ...
Validation Engineer I
Rockville, MD · On-site
Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist ...
Validation Engineer I
Rockville, MD · On-site
Our Validation specialists will be involved with the qualification and requalification of equipment used to manufacture and test biologics/drug product/etc. at client sites. The validation specialist ...
Commissioning / Qualification / Validation Specialist
Columbus, OH · On-site +1
$90K - $100K/yr
CQV Specialists develop and execute CQV protocols (e.g., IQ/OQ/PQ) for these industries. Protocols ... Lead validation specialists in the execution of project tasks. * Perform other related duties as ...
Commissioning / Qualification / Validation Specialist
Columbus, OH · On-site +1
$90K - $100K/yr
CQV Specialists develop and execute CQV protocols (e.g., IQ/OQ/PQ) for these industries. Protocols ... Lead validation specialists in the execution of project tasks. * Perform other related duties as ...
CQV Specialists develop and execute CQV protocols (e.g., IQ/OQ/PQ) for these industries. Protocols ... Lead validation specialists in the execution of project tasks. * Perform other related duties as ...
CQV Specialists develop and execute CQV protocols (e.g., IQ/OQ/PQ) for these industries. Protocols ... Lead validation specialists in the execution of project tasks. * Perform other related duties as ...
Validation Specialist
Aibonito, PR · On-site
Validation Specialist Key Responsibilities: * Develop, review, and execute Validation Master Plans (VMPs) and validation protocols, including IQ, OQ, and PQ . * Validate and qualify equipment ...
Validation Specialist
Aibonito, PR · On-site
Validation Specialist Key Responsibilities: * Develop, review, and execute Validation Master Plans (VMPs) and validation protocols, including IQ, OQ, and PQ . * Validate and qualify equipment ...
Provides guidance, advice, feedback and support to more junior level validation specialists * Provides technical support and guidance on Deviations, Standard Operating Procedures (SOPs), Work ...
Provides guidance, advice, feedback and support to more junior level validation specialists * Provides technical support and guidance on Deviations, Standard Operating Procedures (SOPs), Work ...
Qualification & Validation Senior Specialist
Bloomsbury, NJ · On-site
$65K - $89K/yr
Provides guidance, advice, feedback and support to more junior level validation specialists * Provides technical support and guidance on Deviations, Standard Operating Procedures (SOPs), Work ...
Qualification & Validation Senior Specialist
Bloomsbury, NJ · On-site
$65K - $89K/yr
Provides guidance, advice, feedback and support to more junior level validation specialists * Provides technical support and guidance on Deviations, Standard Operating Procedures (SOPs), Work ...
Position: Validation Engineer / Validation Specialist Location: Maryland Duration: Long Term Job Overview We are seeking an experienced Validation Engineer / Validation Specialist to support ...
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Position: Validation Engineer / Validation Specialist Location: Maryland Duration: Long Term Job Overview We are seeking an experienced Validation Engineer / Validation Specialist to support ...
Validation Specialist
Aibonito, PR · On-site
$60 - $80/hr
Aibonito, Puerto Rico | Posted on 08/04/2026 We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes. Requirements * 3 to 5 ...
Validation Specialist
Aibonito, PR · On-site
$60 - $80/hr
Aibonito, Puerto Rico | Posted on 08/04/2026 We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes. Requirements * 3 to 5 ...
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...
The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and ...
MD · On-site
Validation Engineer / Validation Specialist Location: Maryland Duration: Long-Term Contract Job Overview We are seeking an experienced Validation Engineer/Validation Specialist to support equipment ...
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MD · On-site
Validation Engineer / Validation Specialist Location: Maryland Duration: Long-Term Contract Job Overview We are seeking an experienced Validation Engineer/Validation Specialist to support equipment ...
Validation Specialist
Marion, NC · On-site
Validation Specialist Marion, NC, USA 12 months W2 contract Must have experience supporting medical device manufacturing under ISO 13485 Writing test protocols within KNEAT Gx Knowledge of CQV ...
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Validation Specialist
Marion, NC · On-site
Validation Specialist Marion, NC, USA 12 months W2 contract Must have experience supporting medical device manufacturing under ISO 13485 Writing test protocols within KNEAT Gx Knowledge of CQV ...
Validation Specialists information
See salary details
$15.87 - $21.28
3% of jobs
$21.28 - $26.70
3% of jobs
$26.70 - $32.12
3% of jobs
$32.12 - $37.54
8% of jobs
$39.98 is the 25th percentile. Wages below this are outliers.
$37.54 - $42.96
16% of jobs
$42.96 - $48.38
9% of jobs
The median wage is $50.58 / hr.
$48.38 - $53.80
17% of jobs
$58.95 is the 75th percentile. Wages above this are outliers.
$53.80 - $59.22
16% of jobs
$59.22 - $64.64
8% of jobs
$64.64 - $70.06
7% of jobs
$70.06 - $75.48
8% of jobs
$15
$50
$75
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Laboratory Systems Validation Specialists
San Francisco, CA • On-site
Full-time
Re-posted 18 days ago
Key responsibilities
Define validation requirements and develop systems validation documentation.
Generate and execute test protocols, including functional testing and validation reports.
Assist in managing computer systems validation and ensure compliance with regulatory guidelines.
Job description
LabAnswer is the leading and largest laboratory informatics consultancy; combining science, laboratory, regulatory and information technologies. We have the people, processes, methodologies, IP and experience to deliver comprehensive laboratory informatics solutions.
LabAnswer has architected, implemented, deployed and/or supported hundreds of major scientific informatics systems across more than a thousand laboratories. LabAnswer performs significant laboratory automation work in pharmaceuticals, bio-pharmaceuticals, medical devices, forensics, and life sciences research laboratories spanning research, development and manufacturing/QC operations.
The LabAnswer team has a rare combination of laboratory science, IT, business and regulatory expertise. We specialize in helping companies strategize, architect, implement and support scientific data management and laboratory automation projects.
The Laboratory Systems Validation Specialist position will be responsible for defining validation requirements, developing systems validation documentation, generating and executing test protocols and summarizing validation activities in reports. The selected individual will play a key role throughout the system development life cycle (SDLC), from validation of complete new systems on projects through qualification of changes for existing systems, to assure that all critical systems remain in a validated state. Their focus will be on computerized systems in support of the Pharmaceutical, Biotechnology and Medical Device industries, including but not limited to manufacturing, laboratory and clinical applications as well as business systems. This position is based in the San Francisco Bay area so travel is limited if you are residing in this location.
Responsibilities (including but not limited to):
Assists in the management of computer systems validation
Assists in defining validation strategy
Qualification / validation of automated test management tools, specifically Mercury TestDirector for Quality Center and QuickTest Professional
Generation of validation documentation, which include validation plans, audit plans, requirement specifications, test plans, IQ, OQ and PQ protocols, test cases/scripts, traceability matrices and validation reports
Development and execution of functional testing, both manual and automated
Conducting risk assessments and periodic audits of systems and software development activities
Ensures all systems and software are in compliance with GMP, GLP, GCP, QSR, 21 CFR Part 11, ICH guidelines, and GAMP guidelines
Assists in the management of controlled documents
Responsible for training related to validation projects, client-specific software applications and SOPs
Development of SOPs in support of quality systems and software development
Minimum Requirements (education and work experience):
BS or MS in computer science, life sciences, engineering or equivalent work experience with 2 - 5 years validation experience in the biotechnology, pharmaceutical or medical device industries
Working knowledge of GMP, GLP, GCP, QSR, GAMP and 21 CFR Part 11 as they relate to computer systems validation
LabWare LIMS validation experience
Knowledgeable in applying SOPs, work instructions and regulatory requirements to the System Development Life Cycle
Experience with testing and supporting manufacturing, laboratory and clinical applications as well as business systems is helpful. (i.e. MES, PLC, SCADA, LIMS, CDAS, CDMS, EDC, CTMS, SAP)
Experience with Client Server, RDMS Database ( Oracle, Sql server, etc), and Web applications
Experience in software development life cycle for computer systems
Excellent written and verbal communication skills, with hands-on experience working in a systems development environment, and as a productive and supportive member of a multidisciplinary project team
Education:
Bachelor Degree in chemistry or related discipline or related experience
At LabAnswer we offer a very competitive
compensation package based on experience and education. We are looking for
excellent people to join our team, those who are looking to join a company for
the long term. Our consultants are team players and are the best at what they
do. Please read our employee value proposition and philosophy statement at www.labanswer.com to see if you are the right match for LabAnswer
About LabAnswer
Sourced by ZipRecruiter
Company size
201 - 500 Employees
Headquarters location
Sugar Land, TX, US
Year founded
1990