Validation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desired * Excellent leadership skills including the ability to simultaneously ...
Validation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desired * Excellent leadership skills including the ability to simultaneously ...
Validation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desired * Excellent leadership skills including the ability to simultaneously ...
Validation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desired * Excellent leadership skills including the ability to simultaneously ...
Validation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desired * Excellent leadership skills including the ability to simultaneously ...
Validation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desired * Excellent leadership skills including the ability to simultaneously ...
Expertise in scientific / technical subject areas - Equipment Qualification, Computer System Validation, SCADA system architecture, Biotech Process Equipment/Systems. * Proficient in use of ...
Expertise in scientific / technical subject areas - Equipment Qualification, Computer System Validation, SCADA system architecture, Biotech Process Equipment/Systems. * Proficient in use of ...
Automation Engineer, GMP
Pennington, NJ · On-site
Expertise in scientific / technical subject areas - Equipment Qualification, Computer System Validation, SCADA system architecture, Biotech Process Equipment/Systems. * Proficient in use of ...
Automation Engineer, GMP
Pennington, NJ · On-site
Expertise in scientific / technical subject areas - Equipment Qualification, Computer System Validation, SCADA system architecture, Biotech Process Equipment/Systems. * Proficient in use of ...
Validation Engineer
New York, NY · On-site
$70K - $80K/yr
Review system requirements, design specifications, and user stories to ensure they are testable and ... Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related field (or ...
Validation Engineer
New York, NY · On-site
$70K - $80K/yr
Review system requirements, design specifications, and user stories to ensure they are testable and ... Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related field (or ...
Expertise in scientific / technical subject areas - Equipment Qualification, Computer System Validation, SCADA system architecture, Biotech Process Equipment/Systems. * Proficient in use of ...
Quick apply
Expertise in scientific / technical subject areas - Equipment Qualification, Computer System Validation, SCADA system architecture, Biotech Process Equipment/Systems. * Proficient in use of ...
Field Computer Specialist
New York, NY · On-site
$5.3K - $5.8K/mo
The position requires a valid driver's license with a clean driving record. A company-provided van ... Security camera systems, DVR/NVRs, coax and IP, including wiring and camera installation ...
Field Computer Specialist
New York, NY · On-site
$5.3K - $5.8K/mo
The position requires a valid driver's license with a clean driving record. A company-provided van ... Security camera systems, DVR/NVRs, coax and IP, including wiring and camera installation ...
Deviation Investigator
Princeton, NJ · On-site
Thorough knowledge of and competence in IT processes, including but not limited to deviations, investigations, CAPA management, SLC, computer system validation, and change management. * Must have ...
Deviation Investigator
Princeton, NJ · On-site
Thorough knowledge of and competence in IT processes, including but not limited to deviations, investigations, CAPA management, SLC, computer system validation, and change management. * Must have ...
BW Design Group is a fully integrated architecture, engineering, construction, system integration ... Strong computer skills (Microsoft Office, Microsoft Project, & AutoCAD) * Willing and able to ...
BW Design Group is a fully integrated architecture, engineering, construction, system integration ... Strong computer skills (Microsoft Office, Microsoft Project, & AutoCAD) * Willing and able to ...
Validation Engineer
East Brunswick, NJ · On-site
BW Design Group is a fully integrated architecture, engineering, construction, system integration ... Strong computer skills (Microsoft Office, Microsoft Project, & AutoCAD) * Willing and able to ...
Validation Engineer
East Brunswick, NJ · On-site
BW Design Group is a fully integrated architecture, engineering, construction, system integration ... Strong computer skills (Microsoft Office, Microsoft Project, & AutoCAD) * Willing and able to ...
BW Design Group is a fully integrated architecture, engineering, construction, system integration ... Strong computer skills (Microsoft Office, Microsoft Project, & AutoCAD) * Willing and able to ...
BW Design Group is a fully integrated architecture, engineering, construction, system integration ... Strong computer skills (Microsoft Office, Microsoft Project, & AutoCAD) * Willing and able to ...
Validation Engineer
New York, NY · On-site
Perform CSA/CSV for lab systems (LIMS, Empower, Chromeleon) * Develop validation docs: URS, risk assessments, protocols, reports * Ensure compliance with 21 CFR Part 11, GAMP 5, Data Integrity (ALCOA+
Quick apply
Validation Engineer
New York, NY · On-site
Perform CSA/CSV for lab systems (LIMS, Empower, Chromeleon) * Develop validation docs: URS, risk assessments, protocols, reports * Ensure compliance with 21 CFR Part 11, GAMP 5, Data Integrity (ALCOA+
... systems. • Works 3 days from office in Raritan • Experience with SAP and ERP experience with ... Define and implement Risk based validation activities. • Experience in writing and executing ...
Quick apply
... systems. • Works 3 days from office in Raritan • Experience with SAP and ERP experience with ... Define and implement Risk based validation activities. • Experience in writing and executing ...
This role will develop validation and Quality System documentation (e.g., IQ/OQ/PQ/SOP/Change Controls/Deviations/CAPAs etc.). This role will organize all validation activities ensuring project ...
Quick apply
This role will develop validation and Quality System documentation (e.g., IQ/OQ/PQ/SOP/Change Controls/Deviations/CAPAs etc.). This role will organize all validation activities ensuring project ...
Model Validation Director
New York, NY · On-site +1
The Model Validation Director is expected to lead and execute model validation testing processes on ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...
Model Validation Director
New York, NY · On-site +1
The Model Validation Director is expected to lead and execute model validation testing processes on ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...
Model Validation Director
New York, NY · On-site
The Model Validation Director is expected to lead and execute model validation testing processes on ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...
Model Validation Director
New York, NY · On-site
The Model Validation Director is expected to lead and execute model validation testing processes on ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...
Validation Engineer
Hillsborough, NJ · On-site
R3 Technology Inc. seeks Validation Engineer or it Hillsborough NJ office to gather requirements to develop product-level requirements and assist with high level systems view of product design.
Validation Engineer
Hillsborough, NJ · On-site
R3 Technology Inc. seeks Validation Engineer or it Hillsborough NJ office to gather requirements to develop product-level requirements and assist with high level systems view of product design.
This includes optimizing systems that support the work in and around this area of responsibility ... Computer, Equipment, Cleaning, Process, etc.) * A technical background in medical devices ...
This includes optimizing systems that support the work in and around this area of responsibility ... Computer, Equipment, Cleaning, Process, etc.) * A technical background in medical devices ...
It encompasses a Quality Operations division that handles Computer System Validation (CSV), QMS Management, and Commercial Quality Shared Services, including specialized support for Transportation ...
It encompasses a Quality Operations division that handles Computer System Validation (CSV), QMS Management, and Commercial Quality Shared Services, including specialized support for Transportation ...
Computer System Validation information
See Princeton, NJ salary details
$11.18 - $18.44
2% of jobs
$18.44 - $25.70
9% of jobs
$25.70 - $32.95
1% of jobs
$32.95 - $40.21
4% of jobs
$44.61 is the 25th percentile. Wages below this are outliers.
$40.21 - $47.47
15% of jobs
$47.47 - $54.72
9% of jobs
The median wage is $60.77 / hr.
$54.72 - $61.98
13% of jobs
$67.76 is the 75th percentile. Wages above this are outliers.
$61.98 - $69.23
29% of jobs
$69.23 - $76.49
12% of jobs
$76.49 - $83.75
2% of jobs
$83.75 - $91
5% of jobs
$11
$57
$91
How much do computer system validation jobs pay per hour?
What are some typical challenges faced in Computer System Validation roles?
Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.
What is a Computer System Validation job?
A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.
What is the salary of computer system validation?
What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?
To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.
What is the work of computer system validation?
Is computer system validation a good field?
Is CSV a skill?
Full-time
Posted 23 days ago
Job description
About Us:
BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.
Job Description:
Project Manager, Validation
Who You'll Work With
You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to make an impact. You will be valued, cared for, and challenged on your path to becoming a world-class professional consultant and surrounded by leaders who are committed to creating an environment that enables you to realize your own success and fulfillment.
When you join Design Group as a Project Manager, Validation, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world's leading companies solve their most difficult problems. You will join our Regulatory Compliance Practice and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy.
What You'll Do
You'll work individually and in teams to support capital projects and implement solutions for our clients. Together, you will help our clients make critical changes to improve their performance and realize their most important goals.
- Responsible for preparing, executing commissioning and qualification documents for a variety of utility, facility, and process equipment.
- Lead and manage a diverse portfolio of validation projects simultaneously (equipment qualification, process validation, cleaning validation, system digitization, etc.)
- Develop and execute a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment.
- Serve as the primary on-site point of contact and local engineering leader for major pharmaceutical manufacturing clients
- Build and maintain strong relationships with client stakeholders across operations, quality, regulatory, and executive levels
- Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team
What You'll Bring
- Minimum 10+ years of demonstrated experience with validation of pharmaceutical or medical device processes and equipment
- FAT, SAT, IQ and OQ documentation development and execution on Automated Systems in the Pharmaceutical Industry
- Validation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desired
- Excellent leadership skills including the ability to simultaneously organize, and successfully execute multiple project responsibilities
- Candidates need to possess good communication and interpersonal skills and the ability to interact with all levels of management, clients, and vendors.
- Strong computer skills are also required
- Willing and able to travel as necessary for project requirements to include but not be limited to: project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc.
- Bachelor's degree in Chemical Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering or equivalent technical degree.
Our culture and commitment to our people is what sets us apart. We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our model and entrepreneurial mindset offer a rewarding, challenging, and highly flexible path. As a Sr. Validation Engineer, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First Year Experience program, Individual Development Plans, and Career Path resources and tools. You will be surrounded by exceptional talent who will support your development as both a world-class engineer and a highly effective leader.
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Feel like you're on the path to becoming a Project Manager, Validation but you're not quite there yet? We'd love to connect with you to see if we can take you from where you are today and grow you into a Design Group Engineering Consultant.
At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work-therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process.
Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.
Company:
Design Group