Strong computer skills are also required * Willing and able to travel as necessary for project ... As a Sr. Validation Engineer, you will build a meaningful and fulfilling career with the support of ...
Strong computer skills are also required * Willing and able to travel as necessary for project ... As a Sr. Validation Engineer, you will build a meaningful and fulfilling career with the support of ...
Validation Engineer II
Branchburg, NJ · On-site
$75K/yr
Preferred Bachelor's degree in engineering , science or computer science is Highly Desired. 3+ years validation experience writing and executing ( IQ/OQ/PQ ) with systems and equipment on the shop ...
Validation Engineer II
Branchburg, NJ · On-site
$75K/yr
Preferred Bachelor's degree in engineering , science or computer science is Highly Desired. 3+ years validation experience writing and executing ( IQ/OQ/PQ ) with systems and equipment on the shop ...
Validation Associate Consultant
Princeton, NJ · On-site
$112K - $123K/yr
Bachelor's or Master's degree in Engineering, Science, Medical, or a related field. * 3+ years of hands-on experience in Computer System Validation within GxP-regulated environments (GCP/GMP; FDA, EU ...
Validation Associate Consultant
Princeton, NJ · On-site
$112K - $123K/yr
Bachelor's or Master's degree in Engineering, Science, Medical, or a related field. * 3+ years of hands-on experience in Computer System Validation within GxP-regulated environments (GCP/GMP; FDA, EU ...
Understanding of working in a regulated environment, or understanding of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation ...
Understanding of working in a regulated environment, or understanding of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation ...
Model Validation Expert
New York, NY · On-site
... Computer Science, Econometrics, or related quantitative field 10+ years of experience in quantitative modeling, model validation, or model risk management Deep expertise in pricing, risk, statistical ...
Model Validation Expert
New York, NY · On-site
... Computer Science, Econometrics, or related quantitative field 10+ years of experience in quantitative modeling, model validation, or model risk management Deep expertise in pricing, risk, statistical ...
Senior Validation Manager
Princeton, NJ · On-site
Validation activities include Facility/Clean rooms, manufacturing equipment, laboratory instrument, computer system, cleaning, and manufacturing processes in an aseptic environment. In this role, you ...
Senior Validation Manager
Princeton, NJ · On-site
Validation activities include Facility/Clean rooms, manufacturing equipment, laboratory instrument, computer system, cleaning, and manufacturing processes in an aseptic environment. In this role, you ...
(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
Senior Validation Manager
Princeton, NJ · On-site
Validation activities include Facility/Clean rooms, manufacturing equipment, laboratory instrument, computer system, cleaning, and manufacturing processes in an aseptic environment. In this role, you ...
Quick apply
Senior Validation Manager
Princeton, NJ · On-site
Validation activities include Facility/Clean rooms, manufacturing equipment, laboratory instrument, computer system, cleaning, and manufacturing processes in an aseptic environment. In this role, you ...
(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
Quick apply
(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
Quick apply
(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
(Sr.) Validation Engineer
Pennington, NJ · On-site
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
(Sr.) Validation Engineer
Pennington, NJ · On-site
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
Thorough knowledge of computer validation/SDLC principles and automation change control procedures. (e.g., GAMP 5) * Strong technical competency with knowledge of pharmaceutical industry processes ...
New
Thorough knowledge of computer validation/SDLC principles and automation change control procedures. (e.g., GAMP 5) * Strong technical competency with knowledge of pharmaceutical industry processes ...
New
... Computer System Validation- Life Sciences We are looking for smart, self-driven, high-energy people with intellectual curiosity and passion for excellence; specifically, we are looking for candidates ...
... Computer System Validation- Life Sciences We are looking for smart, self-driven, high-energy people with intellectual curiosity and passion for excellence; specifically, we are looking for candidates ...
Bachelor's Degree in Computer Science, Computer Engineering or related discipline * Experience implementing software verification and validation processes, automation techniques, and testing ...
Bachelor's Degree in Computer Science, Computer Engineering or related discipline * Experience implementing software verification and validation processes, automation techniques, and testing ...
... computer validation/SDLC principles and automation change control procedures. (e.g., GAMP 5) • Strong technical competency with knowledge of pharmaceutical industry processes & practices.
New
... computer validation/SDLC principles and automation change control procedures. (e.g., GAMP 5) • Strong technical competency with knowledge of pharmaceutical industry processes & practices.
New
Senior Engineer I, Validation
Cranbury, NJ · On-site
$73K - $117K/yr
Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices. * Experience in the qualification of biologics ...
Senior Engineer I, Validation
Cranbury, NJ · On-site
$73K - $117K/yr
Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices. * Experience in the qualification of biologics ...
Undergraduate degree in Computer Science, Data Science, Artificial Intelligence, Applied ... Lead end-to-end validation of AI, GenAI, and Agentic AI solutions, from initial review of ...
Undergraduate degree in Computer Science, Data Science, Artificial Intelligence, Applied ... Lead end-to-end validation of AI, GenAI, and Agentic AI solutions, from initial review of ...
... computer validation/SDLC principles and automation change control procedures. (e.g., GAMP 5) • Strong technical competency with knowledge of pharmaceutical industry processes & practices.
New
... computer validation/SDLC principles and automation change control procedures. (e.g., GAMP 5) • Strong technical competency with knowledge of pharmaceutical industry processes & practices.
New
Hardware Validation & Lab Operations Engineer
New York, NY · On-site
$120K - $130K/yr
... (CAD tools such as SolidWorks, AutoCAD) Hands-on experience with environmental, mechanical, and ESD test equipment Strong knowledge of metrology tools (CT Scan, CMM) and material analysis (FTIR ...
Hardware Validation & Lab Operations Engineer
New York, NY · On-site
$120K - $130K/yr
... (CAD tools such as SolidWorks, AutoCAD) Hands-on experience with environmental, mechanical, and ESD test equipment Strong knowledge of metrology tools (CT Scan, CMM) and material analysis (FTIR ...
Computer Technician
$18.25 - $24.25/hr
Clear and valid driver's license Special Knowledge/Skills: * Knowledge of computer workstation setup HP Laptops/Desktops, Apple Devices) * Knowledge of computer hardware and software applications
Computer Technician
$18.25 - $24.25/hr
Clear and valid driver's license Special Knowledge/Skills: * Knowledge of computer workstation setup HP Laptops/Desktops, Apple Devices) * Knowledge of computer hardware and software applications
Computer Validation information
See Dayton, NJ salary details
$10.83 - $17.86
2% of jobs
$17.86 - $24.89
9% of jobs
$24.89 - $31.92
1% of jobs
$31.92 - $38.95
4% of jobs
$43.21 is the 25th percentile. Wages below this are outliers.
$38.95 - $45.98
15% of jobs
$45.98 - $53
9% of jobs
The median wage is $58.86 / hr.
$53 - $60.03
13% of jobs
$65.63 is the 75th percentile. Wages above this are outliers.
$60.03 - $67.06
29% of jobs
$67.06 - $74.09
12% of jobs
$74.09 - $81.12
2% of jobs
$81.12 - $88.15
5% of jobs
$10
$55
$88
How much do computer validation jobs pay per hour?
What is the salary of SoC validation engineer?
How to become a validation specialist?
What is the difference between Computer Validation vs Quality Assurance Specialist?
| Aspect | Computer Validation | Quality Assurance Specialist |
|---|---|---|
| Required Credentials | GxP, 21 CFR Part 11, validation certifications | ISO standards, QA certifications, GxP knowledge |
| Work Environment | Pharmaceutical, biotech, regulated industries | Manufacturing, healthcare, regulated industries |
| Employer & Industry Usage | Regulated industries requiring validated systems | Ensuring quality compliance across processes |
Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.
What is the salary of a CSV engineer?
Is computer system validation a good field?
Full-time
Posted 11 days ago
Job description
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.
Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.
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.
Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.
Company:
Design Group