Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...
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Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...
The Validation Engineer is responsible for all equipment and process validation activities at Herbalife Innovation and Manufacturing site, with primary focus at the Lake Forest location. Execution of ...
The Validation Engineer is responsible for all equipment and process validation activities at Herbalife Innovation and Manufacturing site, with primary focus at the Lake Forest location. Execution of ...
Validation Engineer
Hartland, WI · On-site
$73K - $110K/yr
Job Summary Responsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210 ...
Validation Engineer
Hartland, WI · On-site
$73K - $110K/yr
Job Summary Responsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210 ...
Validation Engineer
$89K - $110K/yr
Validation Engineer Position Summary: * Work Schedule: Monday - Friday, 8:00am to 5:00pm * 100% on-site The Chelsea facility is Catalent's global Center of Excellence for spray dry dispersion and Dry ...
Validation Engineer
$89K - $110K/yr
Validation Engineer Position Summary: * Work Schedule: Monday - Friday, 8:00am to 5:00pm * 100% on-site The Chelsea facility is Catalent's global Center of Excellence for spray dry dispersion and Dry ...
Validation Engineer
Philadelphia, PA · On-site
Peregrine Team is hiring a Validation Engineer to support equipment and process validation within a regulated pharmaceutical environment. This role ensures compliance with regulatory standards and ...
Validation Engineer
Philadelphia, PA · On-site
Peregrine Team is hiring a Validation Engineer to support equipment and process validation within a regulated pharmaceutical environment. This role ensures compliance with regulatory standards and ...
Validation Specialist
Indianapolis, IN · On-site
I am reaching out regarding an exciting opportunity for a Validation Specialist position with one of our prestigious medical device clients. We are seeking professionals with experience in GMP ...
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Validation Specialist
Indianapolis, IN · On-site
I am reaching out regarding an exciting opportunity for a Validation Specialist position with one of our prestigious medical device clients. We are seeking professionals with experience in GMP ...
Validation Specialist
Rochester, NY · On-site
Position Summary The Validation Specialist is responsible for supporting and executing validation and qualification activities for manufacturing processes, equipment, utilities, and facilities in a ...
Validation Specialist
Rochester, NY · On-site
Position Summary The Validation Specialist is responsible for supporting and executing validation and qualification activities for manufacturing processes, equipment, utilities, and facilities in a ...
Validation Lead
Raritan, NJ · On-site
Role - Validation Lead Location -Raritan, NJ(Hybrid) Job Details: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on experience in retro-validation ...
New
Validation Lead
Raritan, NJ · On-site
Role - Validation Lead Location -Raritan, NJ(Hybrid) Job Details: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on experience in retro-validation ...
New
PR · On-site
Validation Manager About Ocyonbio: OcyonBio is a biotechnology CDMO based in Aguadilla, Puerto Rico, providing flexible cGMP facilities and integrated services to accelerate the development ...
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PR · On-site
Validation Manager About Ocyonbio: OcyonBio is a biotechnology CDMO based in Aguadilla, Puerto Rico, providing flexible cGMP facilities and integrated services to accelerate the development ...
Validation Engineer
$103K - $142K/yr
A brief overview The Quality Engineer (QE) / Validation fulfills a critical role in GMP operations, supporting cleaning validation activities for API and PMO manufacturing, and the qualification of ...
Validation Engineer
$103K - $142K/yr
A brief overview The Quality Engineer (QE) / Validation fulfills a critical role in GMP operations, supporting cleaning validation activities for API and PMO manufacturing, and the qualification of ...
Validation Engineer
San Diego, CA · On-site
Validation Engineer Location: San Diego, CA Duration: Longterm Job Summary: A Validation Engineer to lead and support quality-related validation activities within the Quality Management System. The ...
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Validation Engineer
San Diego, CA · On-site
Validation Engineer Location: San Diego, CA Duration: Longterm Job Summary: A Validation Engineer to lead and support quality-related validation activities within the Quality Management System. The ...
Director, Validation
Philadelphia, PA · On-site +1
Director, Validation: Remote OR Hybrid - Philadelphia, PA Cabaletta Bio (Nasdaq: CABA) is a late-stage clinical biotechnology company focused on developing and launching curative targeted cell ...
Director, Validation
Philadelphia, PA · On-site +1
Director, Validation: Remote OR Hybrid - Philadelphia, PA Cabaletta Bio (Nasdaq: CABA) is a late-stage clinical biotechnology company focused on developing and launching curative targeted cell ...
Director, Validation
Bedford, NH · On-site
$120 - $160/hr
The Validation Director will also schedule the appropriate resources for assistance with validation, to meet the established production schedule, vendor/contract activities in the cleanrooms ...
New
Director, Validation
Bedford, NH · On-site
$120 - $160/hr
The Validation Director will also schedule the appropriate resources for assistance with validation, to meet the established production schedule, vendor/contract activities in the cleanrooms ...
New
BWI Group is seeking a Validation Engineer who is responsible for planning, executing, and documenting validation activities for products and systems to ensure compliance with internal requirements ...
BWI Group is seeking a Validation Engineer who is responsible for planning, executing, and documenting validation activities for products and systems to ensure compliance with internal requirements ...
Validation Engineer
Hartland, WI · On-site
$73K - $110K/yr
Job Summary Responsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210 ...
Validation Engineer
Hartland, WI · On-site
$73K - $110K/yr
Job Summary Responsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210 ...
Validation Engineer
Auburn Hills, MI · On-site
The Validation Engineer is responsible for developing validation test plans and timing schedules to support program objectives for the validation of automotive components. These components span a ...
Validation Engineer
Auburn Hills, MI · On-site
The Validation Engineer is responsible for developing validation test plans and timing schedules to support program objectives for the validation of automotive components. These components span a ...
Validation Specialist
Dorado, PR · On-site
For Validation services. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's in Engineering or Sciences with three (3) years of experience in Validation activities within the Medical Devices ...
Validation Specialist
Dorado, PR · On-site
For Validation services. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's in Engineering or Sciences with three (3) years of experience in Validation activities within the Medical Devices ...
The Validation Engineer is responsible for all equipment and process validation activities at Herbalife Innovation and Manufacturing site, with primary focus at the Lake Forest location. Execution of ...
The Validation Engineer is responsible for all equipment and process validation activities at Herbalife Innovation and Manufacturing site, with primary focus at the Lake Forest location. Execution of ...
Validation Engineer
Columbia, SC · On-site
$74K - $97K/yr
The Validation Engineer will be responsible for supporting qualification and validation activities across various systems and processes within the organization. This role ensures that all equipment ...
Validation Engineer
Columbia, SC · On-site
$74K - $97K/yr
The Validation Engineer will be responsible for supporting qualification and validation activities across various systems and processes within the organization. This role ensures that all equipment ...
Validation 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 jobs pay per hour?
What is the difference between Validation vs Quality Assurance?
| Aspect | Validation | Quality Assurance |
|---|---|---|
| Purpose | Ensures products meet specifications and intended use | Prevents defects through process improvements |
| Focus | Product-specific testing and verification | Process and system quality control |
| Activities | Design validation, process validation, equipment validation | Audits, process reviews, standards compliance |
| Timing | Before product release | Throughout production cycle |
Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.
What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?
What are some common challenges faced by professionals in validation roles, and how can they be overcome?
What is a validation job?

Other
Re-posted 19 days ago
Job description
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
- Validation Engineer - Upstream
Description:
We are seeking a Validation Engineer with experience in upstream equipment to join our team. The Validation Engineer will be responsible for validating equipment, processes, and systems used in the manufacturing process to ensure compliance with industry standards and regulations. Knowledge of common upstream equipment in biotech is a plus.
Qualifications:
- Bachelor's degree in Engineering or related field.
- Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.
- Proven experience as a Validation Engineer in a manufacturing environment.
- Strong knowledge of upstream equipment and processes, including but not limited to: fermenters, bioreactors, centrifuges, filtration systems, and chromatography equipment.
- Familiarity with industry regulations and standards.
- Excellent problem-solving skills and attention to detail.
- Effective communication skills and ability to work in a team environment.
- Must be fully bilingual (English / Spanish) with excellent oral skills.
- Must be proficient using MS Windows and Microsoft Office applications.
- Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
- Available to work extended hours, possibility of weekends and holidays.
Responsibilities:
- Develop and execute validation protocols for equipment and processes.
- Coordinate with cross-functional teams to ensure validation requirements are met.
- Analyze validation test results and prepare reports documenting findings.
- Identify and address deviations or non-conformances during the validation process.
- Support continuous improvement initiatives related to equipment validation.
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.