Validation Engineer / Validation Specialist Location: Maryland Duration: Long Term Job Overview We are seeking an experienced Validation Engineer / Validation Specialist to support validation ...
Quick apply
Validation Engineer / Validation Specialist Location: Maryland Duration: Long Term Job Overview We are seeking an experienced Validation Engineer / Validation Specialist to support validation ...
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 ...
Validation Specialist III
Albuquerque, NM · On-site
Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with ...
Validation Specialist III
Albuquerque, NM · On-site
Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with ...
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 ...
Validation Specialist III
Albuquerque, NM · On-site
Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with ...
Validation Specialist III
Albuquerque, NM · On-site
Validation Specialist III in Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with ...
Commissioning / Qualification / Validation Specialist
Columbus, OH · On-site
$80 - $100/hr
... Validation (CQV) services to the life sciences (pharmaceutical / biotech industries), food, and ... CQV Specialists develop and execute CQV protocols (e.g., IQ/OQ/PQ) for these industries. Protocols ...
Commissioning / Qualification / Validation Specialist
Columbus, OH · On-site
$80 - $100/hr
... Validation (CQV) services to the life sciences (pharmaceutical / biotech industries), food, and ... CQV Specialists develop and execute CQV protocols (e.g., IQ/OQ/PQ) for these industries. Protocols ...
Validation Specialist
Cidra, PR · On-site
$80 - $100/hr
Cidra, Puerto Rico | Posted on 08/06/2026 Validation Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation ...
Validation Specialist
Cidra, PR · On-site
$80 - $100/hr
Cidra, Puerto Rico | Posted on 08/06/2026 Validation Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation ...
Commissioning / Qualification / Validation Specialist
Columbus, OH · On-site
$80 - $100/hr
... Validation (CQV) services to the life sciences (pharmaceutical / biotech industries), food, and ... CQV Specialists develop and execute CQV protocols (e.g., IQ/OQ/PQ) for these industries. Protocols ...
Commissioning / Qualification / Validation Specialist
Columbus, OH · On-site
$80 - $100/hr
... Validation (CQV) services to the life sciences (pharmaceutical / biotech industries), food, and ... CQV Specialists develop and execute CQV protocols (e.g., IQ/OQ/PQ) for these industries. Protocols ...
Validation Specialist
Allentown, PA · On-site
Validation Specialist Position Summary The Validation Specialist will support the qualification of new and existing packaging equipment at the Allentown site. The role is responsible for developing ...
Validation Specialist
Allentown, PA · On-site
Validation Specialist Position Summary The Validation Specialist will support the qualification of new and existing packaging equipment at the Allentown site. The role is responsible for developing ...
Validation Specialist
Rochester, NY · On-site
Validation Specialist Who we are? As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve and simplify patients' lives accessible to as many people as ...
Validation Specialist
Rochester, NY · On-site
Validation Specialist Who we are? As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve and simplify patients' lives accessible to as many people as ...
Jr. Validation Specialist
Carolina, PR · On-site
$60 - $80/hr
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: * Jr. Validation Specialist Position Overview We are seeking a Junior ...
Jr. Validation Specialist
Carolina, PR · On-site
$60 - $80/hr
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: * Jr. Validation Specialist Position Overview We are seeking a Junior ...
Validation Specialist
San Diego, CA · On-site
Job Summary The Operations Validation Specialist at BioLegend will perform and administer validation activities associated with equipment, processes, test methods, facilities and software/systems, in ...
Validation Specialist
San Diego, CA · On-site
Job Summary The Operations Validation Specialist at BioLegend will perform and administer validation activities associated with equipment, processes, test methods, facilities and software/systems, in ...
Validation Specialist
Ottawa, IL · On-site
Position Overview The Validation Specialist ensures that all manufacturing processes, equipment, and products within the health and beauty industry meet regulatory, quality, and safety standards.
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Validation Specialist
Ottawa, IL · On-site
Position Overview The Validation Specialist ensures that all manufacturing processes, equipment, and products within the health and beauty industry meet regulatory, quality, and safety standards.
Validation Specialist
Allentown, PA · On-site
Validation Specialist Position Summary The Validation Specialist will support the qualification of new and existing packaging equipment at the Allentown site. The role is responsible for developing ...
Validation Specialist
Allentown, PA · On-site
Validation Specialist Position Summary The Validation Specialist will support the qualification of new and existing packaging equipment at the Allentown site. The role is responsible for developing ...
Validation Specialist
Allentown, PA · On-site
Validation Specialist Position Summary The Validation Specialist will support the qualification of new and existing packaging equipment at the Allentown site. The role is responsible for developing ...
Quick apply
Validation Specialist
Allentown, PA · On-site
Validation Specialist Position Summary The Validation Specialist will support the qualification of new and existing packaging equipment at the Allentown site. The role is responsible for developing ...
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 ...
Validation Specialist
Champaign, IL · On-site
$60 - $80/hr
Global Product Development Manager Status : Full-Time/Non-Exempt Summary The Validation Specialist is responsible for supporting product validation activities through dimensional measurement, data ...
Validation Specialist
Champaign, IL · On-site
$60 - $80/hr
Global Product Development Manager Status : Full-Time/Non-Exempt Summary The Validation Specialist is responsible for supporting product validation activities through dimensional measurement, data ...
Validation Specialist
Champaign, IL · On-site
$60 - $80/hr
Global Product Development Manager Status : Full-Time/Non-Exempt Summary The Validation Specialist is responsible for supporting product validation activities through dimensional measurement, data ...
Validation Specialist
Champaign, IL · On-site
$60 - $80/hr
Global Product Development Manager Status : Full-Time/Non-Exempt Summary The Validation Specialist is responsible for supporting product validation activities through dimensional measurement, data ...
Validation Specialist
Saddle Brook, NJ · On-site
Validation Specialist Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device IT & Human Resources disciplines in New Jersey. The ...
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Validation Specialist
Saddle Brook, NJ · On-site
Validation Specialist Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device IT & Human Resources disciplines in New Jersey. The ...
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
How much do validation specialists jobs pay per hour?
As of Sep 9, 2026, the average hourly pay for validation specialists in the United States is $50.45, according to ZipRecruiter salary data. Most workers in this role earn between $39.66 and $61.30 per hour, depending on experience, location, and employer.
What are popular job titles related to Validation Specialists jobs?
For Validation Specialists jobs, the most frequently searched job titles are:
Validation Engineer / Validation Specialist
Frederick, MD • On-site
Stark Pharma Solutions Inc
Contractor
Re-posted 6 hours ago
Job description
Position: Validation Engineer / Validation Specialist
Location: Maryland
Duration: Long Term
Job Overview
We are seeking an experienced Validation Engineer / Validation Specialist to support validation activities within a GMP manufacturing facility. The successful candidate will be responsible for preparing and executing qualification protocols, generating validation documentation, supporting equipment and utility validation, and ensuring compliance with cGMP and Good Documentation Practices.
Key Responsibilities
- Prepare and execute IQ/OQ/PQ/RQ protocols and reports for new and existing equipment and utilities.
- Develop acceptance criteria based on industry standards, manufacturer recommendations, user/functional specifications, and current cGMP requirements.
- Generate validation summary reports in accordance with Good Documentation Practices (GDP).
- Perform thermal mapping studies using Kaye AVS or Veriteq dataloggers.
- Develop and revise Standard Operating Procedures (SOPs).
- Analyze validation data and verify compliance with established acceptance criteria.
- Document and support resolution of deviations associated with qualification activities.
- Assist with Commissioning, FAT, and SAT activities as required.
- Prepare technical documentation including validation reports, gap assessments, and risk assessments.
- Provide technical and investigative support for troubleshooting and resolving manufacturing equipment issues.
- Perform technical reviews of qualification and validation documents prepared by other team members.
- Support facility and validation activities related to regulatory and client audits.
Required Qualifications
- Bachelor's degree in Engineering, Science, or a related field.
- Minimum 4 years of applicable validation experience with a bachelor's degree, or 8 years of applicable experience in lieu of a bachelor's degree.
- Hands-on validation experience in GMP biotechnology or pharmaceutical manufacturing environments.
- Experience with IQ/OQ/PQ/RQ qualification activities.
- Strong working knowledge of cGMP and Good Documentation Practices.
- Experience and knowledge of aseptic processing.
- Hands-on experience with sterilization equipment, cleanroom environments, cleaning processes, and critical utilities such as HVAC, WFI, RO, and CCA.
- Knowledge of computerized control systems and isolator technology.
- Experience using Microsoft Office and electronic systems such as EDMS, RAM, and LIMS.
- Strong written and verbal communication skills with excellent attention to detail.
- Ability to manage multiple projects and work effectively both independently and as part of a team.
- General knowledge of maintenance and calibration procedures is desirable.