Validation Engineer, you are joining a team that will challenge you andposition you for growth. In this role, you will work witha team ofindustry experts to helpthe world's leading companiessolve ...
Validation Engineer, you are joining a team that will challenge you andposition you for growth. In this role, you will work witha team ofindustry experts to helpthe world's leading companiessolve ...
Sr. Validation Engineer
Indianapolis, IN · On-site
Validation & Compliance Activities: * Assist basic and conceptual design phases of capital projects by working with clients and vendors on embedding compliance, testability and lifecycle thinking ...
Sr. Validation Engineer
Indianapolis, IN · On-site
Validation & Compliance Activities: * Assist basic and conceptual design phases of capital projects by working with clients and vendors on embedding compliance, testability and lifecycle thinking ...
Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential ...
Quick apply
Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential ...
Validation Engineer, you are joining a team that will challenge you andposition you for growth. In this role, you will work witha team ofindustry experts to helpthe world's leading companiessolve ...
Validation Engineer, you are joining a team that will challenge you andposition you for growth. In this role, you will work witha team ofindustry experts to helpthe world's leading companiessolve ...
Process & Validation Expert
$97K - $146K/yr
As the Process & Validation Expert, you will execute and manage process, primary packaging, and cleaning validation activities and change management activities to meet cGMP requirements on time and ...
Process & Validation Expert
$97K - $146K/yr
As the Process & Validation Expert, you will execute and manage process, primary packaging, and cleaning validation activities and change management activities to meet cGMP requirements on time and ...
Embedded Validation Engineer - Telematics Location: Columbus, IN Job Type: Full-Time Job Summar yWe are seeking a highly motivated Embedded Validation Enginee r to join our engineering team in ...
Embedded Validation Engineer - Telematics Location: Columbus, IN Job Type: Full-Time Job Summar yWe are seeking a highly motivated Embedded Validation Enginee r to join our engineering team in ...
* Lead the BMS validation lifecycle across all 8 LMF buildings, from URS authoring through Validation Summary Report and closeout. * Author and obtain approval for User Requirement Specifications (URS ...
* Lead the BMS validation lifecycle across all 8 LMF buildings, from URS authoring through Validation Summary Report and closeout. * Author and obtain approval for User Requirement Specifications (URS ...
CQV / Validation Engineer Responsibilities: Commissioning, Qualification & Validation (CQV) * Execute commissioning, qualification, and validation activities for manufacturing equipment, utilities ...
CQV / Validation Engineer Responsibilities: Commissioning, Qualification & Validation (CQV) * Execute commissioning, qualification, and validation activities for manufacturing equipment, utilities ...
The Principal Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance Qualification (Stage 2), and Continued Process Verification (Stage 3) ...
Quick apply
The Principal Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance Qualification (Stage 2), and Continued Process Verification (Stage 3) ...
The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
The Computer Systems Validation Engineer supports validation lifecycle activities for automation and control systems within a regulated pharmaceutical manufacturing environment. This role works ...
Validation Summary Reports * Traceability Matrices * Risk Assessments * Support startup and operational readiness activities for new production equipment and manufacturing systems. * Perform field ...
Validation Summary Reports * Traceability Matrices * Risk Assessments * Support startup and operational readiness activities for new production equipment and manufacturing systems. * Perform field ...
Validation Summary Reports * Traceability Matrices * Risk Assessments * Support startup and operational readiness activities for new production equipment and manufacturing systems. * Perform field ...
Quick apply
Validation Summary Reports * Traceability Matrices * Risk Assessments * Support startup and operational readiness activities for new production equipment and manufacturing systems. * Perform field ...
The Principal Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance Qualification (Stage 2), and Continued Process Verification (Stage 3) ...
The Principal Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance Qualification (Stage 2), and Continued Process Verification (Stage 3) ...
Senior Validation Engineer
Bloomington, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...
Senior Validation Engineer
Bloomington, IN · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...
The Senior Process Validation Engineer is a key member of the Technical Services organization, responsible for leading and supporting validation activities for sterile injectable manufacturing ...
The Senior Process Validation Engineer is a key member of the Technical Services organization, responsible for leading and supporting validation activities for sterile injectable manufacturing ...
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...
Quick apply
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...
The Senior Process Validation Engineer is a key member of the Technical Services organization, responsible for leading and supporting validation activities for sterile injectable manufacturing ...
The Senior Process Validation Engineer is a key member of the Technical Services organization, responsible for leading and supporting validation activities for sterile injectable manufacturing ...
Software Validation Engineer III
Warsaw, IN · On-site
The Software Validation Engineer will be responsible for performing validation activities as new or implemented software within the operations, quality or other functions. Strong and in-depth ...
Software Validation Engineer III
Warsaw, IN · On-site
The Software Validation Engineer will be responsible for performing validation activities as new or implemented software within the operations, quality or other functions. Strong and in-depth ...
The Principal Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance Qualification (Stage 2), and Continued Process Verification (Stage 3) ...
The Principal Quality Process Validation Specialist provides QA oversight of Process Design (Stage 1), Process Performance Qualification (Stage 2), and Continued Process Verification (Stage 3) ...
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...
Quick apply
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...
Validation information
See Indiana salary details
$21.50 - $26.31
2% of jobs
$26.31 - $31.11
6% of jobs
$31.11 - $35.91
13% of jobs
$37.41 is the 25th percentile. Wages below this are outliers.
$35.91 - $40.72
13% of jobs
$40.72 - $45.52
11% of jobs
The median wage is $47.92 / hr.
$45.52 - $50.32
12% of jobs
$50.32 - $55.13
9% of jobs
$58.83 is the 75th percentile. Wages above this are outliers.
$55.13 - $59.93
13% of jobs
$59.93 - $64.73
13% of jobs
$64.73 - $69.54
6% of jobs
$69.54 - $74.34
3% of jobs
$21
$49
$74
How much do validation jobs pay per hour?
What is a validation job?
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 is the 3 month rule for jobs?
What jobs pay $10,000 a month without a degree?
What engineers make $500,000?
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 are validation jobs?
- Embedded System Validation Engineer
- Computer System Validation Csv Remote
- Freelance Work From Home Computer System Validation Csv
- Verification And Validation Engineer
- Biotech Csv
- Validation Manager
- Computer System Validation
- Commissioning Qualification Validation Cqv
- Summer 21 Cfr Part 11 Validation
- Remote Gxp Systems

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.
Â
Â
Job Description:
Sr. Validation Engineer
WhoYou'llWork With
You will join one of our 45 offices in the US, bepart of a committed team ofover1500 professionals,and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed intoa 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-classprofessional consultantandsurrounded byleaders who are committed to creating an environment that enables you to realize your own success and fulfillment.
When you join Design Group as aSr.Validation Engineer, you are joining a team that will challenge you andposition you for growth. In this role, you will work witha team ofindustry experts to helpthe world's leading companiessolve their most difficult problems. You willjoin ourRegulatory Compliance Practiceandpartner with seasoned leaders, technicalspecialists, and subject matter expertsto deliver the highest quality solutions to our clients with consistency and accuracy.
WhatYou'llDo
You'llwork individually and in teams tosupport capitalproject CQV delivery and individual technical contribution for our clients.Together, you will help our clients make critical changes to improve their performance and realize their most important goals.
Validation & Compliance Activities:
Assistbasic and conceptual design phases of capital projects by working with clients and vendors on embedding compliance, testability and lifecycle thinking into early design
Establish User Requirement Specifications for critical equipment and systems.
Assess risk across various aspects of systems' functions and focus efforts on critical quality aspects. Develop and execute validation and FDA compliance related documents/protocols for pharmaceutical equipment and processes - employing industry's most progressive Digital Validation Tools
Prepare, execute, and manage commissioning and qualification documents for utility, facility, and process equipment
Perform FAT, SAT, IQ, andOQdocumentation development and execution on equipment/systems.
Conduct investigations and troubleshoot validation-related issues
Prepare comprehensive written validation reports.
WhatYou'llBring
Experience Requirements:
Sr. Validation Engineer: Minimum 7+ years demonstrated experience with design, commissioning, validation of automation, packaging drug substance (i.e., pooling, centrifugation, TFF) and/or drug product (i.e.,asepticfilling, inspection) systems/equipment, utilities(i.e.,process, equipment), and/or facilities(i.e.,HVAC,classification, contamination control)pharmaceutical or medical device environments validation
Extensive hands-on experience with GMP-regulated environmentswithknowledgeof regulationandguidance's(i.e., CFRParts210, 211,11), Annex 1,ICHQ7/Q8/Q9,ISPEG2G)
Experiencewith implementingrisk-basedapproaches to validationprojects
Authoring, reviewing andapprovingValidationMaster Plans,risk assessments,deviations, andchange controls.
Technical Skills & Qualifications:
Bachelor's degree in Engineering(Bioengineering, Biomedical, Chemical, Electrical, Mechanical, or equivalent technical degree)
Validation experience in automation, packaging, general drug substance and/or drug product systems/equipment, computer systems, utilities, and/or facilities
Strong technical writing and oral communication skills
Proficiencywith project documentation and computer skills (Microsoft Office, Microsoft Project, AutoCAD)
Experience with entire project lifecycle from concept development through startup (preferred)
Professional Attributes:
Excellent leadership and organizational skills with ability to manage multiple responsibilities
Outstanding communication and interpersonal skills to interact with all levels of management, clients, and vendors
Flexibility with tasks and strong analytical capabilities
Willing and able to travel as necessary for project requirements including installation, startup activities, client meetings, and industry events.
Able to communicateanddeveloplong-lasting relationships withclients and project teams
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. Ourmodel and entrepreneurial mindsetoffer a rewarding, challenging, andhighlyflexible path. As aSr. Validation Engineer, youwill build a meaningful and fulfilling careerwith the support of professional developmentresourcesand mentorshipsincludingourFirst Year Experience program, Individual Development Plans, and Career Pathresourcesand tools.You willbe surrounded by exceptional talentwho will supportyour development as both a world-class engineer andahighly effective leader.#LI-TH1
Feel likeyou'reon the path to becoming aSr. Validation Engineer,butyou'renot quite thereyet?We'dlove 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.
Â
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.
Â
Company:
Design GroupAbout PAPER
Sourced by ZipRecruiter
Industry
Machinery manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Green Bay, WI, US
Year founded
1919