Validation Engineer 2
Fishers, IN · On-site
Design validation plans. Conduct independent verification of testing against specifications. Conduct and document impact and risk assessments with a full understanding of equipment/system/ software ...
Fishers, IN · On-site
Design validation plans. Conduct independent verification of testing against specifications. Conduct and document impact and risk assessments with a full understanding of equipment/system/ software ...
Fishers, IN · On-site
Design validation plans. Conduct independent verification of testing against specifications. Conduct and document impact and risk assessments with a full understanding of equipment/system/ software ...
The Inventory Validation Technician works as a part of an inventory validation team and provides clinical equipment services under the close supervision of TRIMEDX management. Duties include, but are ...
The Inventory Validation Technician works as a part of an inventory validation team and provides clinical equipment services under the close supervision of TRIMEDX management. Duties include, but are ...
Indianapolis, IN · On-site
$18.49/hr
The Inventory Validation Technician works as a part of an inventory validation team and provides clinical equipment services under the close supervision of TRIMEDX management. Duties include, but are ...
Indianapolis, IN · On-site
$18.49/hr
The Inventory Validation Technician works as a part of an inventory validation team and provides clinical equipment services under the close supervision of TRIMEDX management. Duties include, but are ...
Fishers, IN · On-site +1
$95.39K - $153.50K/yr
Design validation plans. Conduct independent verification of testing against specifications. Conduct and document impact and risk assessments with a full understanding of equipment/system/ software ...
Fishers, IN · On-site +1
$95.39K - $153.50K/yr
Design validation plans. Conduct independent verification of testing against specifications. Conduct and document impact and risk assessments with a full understanding of equipment/system/ software ...
Fishers, IN · On-site +1
$95.39K - $153.50K/yr
Design validation plans. Conduct independent verification of testing against specifications. Conduct and document impact and risk assessments with a full understanding of equipment/system/ software ...
Quick apply
Fishers, IN · On-site +1
$95.39K - $153.50K/yr
Design validation plans. Conduct independent verification of testing against specifications. Conduct and document impact and risk assessments with a full understanding of equipment/system/ software ...
Validation Engineer (Automotive) Job Location: New Carlisle, IN (Onsite) Job Type: Full-Time * Bachelor's degree in engineering * Establishes vehicle level attributes and requirements. * Leads ...
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Validation Engineer (Automotive) Job Location: New Carlisle, IN (Onsite) Job Type: Full-Time * Bachelor's degree in engineering * Establishes vehicle level attributes and requirements. * Leads ...
Indianapolis, IN · On-site
$18.49/hr
The Inventory Validation Technician works as a part of an inventory validation team and provides clinical equipment services under the close supervision of TRIMEDX management. Duties include, but are ...
Indianapolis, IN · On-site
$18.49/hr
The Inventory Validation Technician works as a part of an inventory validation team and provides clinical equipment services under the close supervision of TRIMEDX management. Duties include, but are ...
Indianapolis, IN · On-site
$72.80K - $80.10K/yr
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 ...
Indianapolis, IN · On-site
$72.80K - $80.10K/yr
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 ...
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 ...
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 ...
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 ...
Fishers, IN · On-site
TSMS - Manager of Process Validation The Technical Services and Manufacturing Sciences (TSMS) Manager of Process Validation will lead and manage a team of technical professionals while providing ...
Fishers, IN · On-site
TSMS - Manager of Process Validation The Technical Services and Manufacturing Sciences (TSMS) Manager of Process Validation will lead and manage a team of technical professionals while providing ...
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 ...
Valspec--a global provider of system validation and lifecycle services--provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999 ...
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Valspec--a global provider of system validation and lifecycle services--provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999 ...
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 ...
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 ...
Fishers, IN · On-site
Description TSMS - Manager of Process Validation The Technical Services and Manufacturing Sciences (TSMS) Manager of Process Validation will lead and manage a team of technical professionals while ...
Fishers, IN · On-site
Description TSMS - Manager of Process Validation The Technical Services and Manufacturing Sciences (TSMS) Manager of Process Validation will lead and manage a team of technical professionals while ...
$97.60K - $146.40K/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 ...
$97.60K - $146.40K/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 ...
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 ...
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 ...
Job Summary: * The Process Validation Engineer supports medical device manufacturing by developing, executing, and maintaining validated manufacturing and test processes. * The role ensures ...
Job Summary: * The Process Validation Engineer supports medical device manufacturing by developing, executing, and maintaining validated manufacturing and test processes. * The role ensures ...
TSMS - Manager of Process Validation The Technical Services and Manufacturing Sciences (TSMS) Manager of Process Validation will lead and manage a team of technical professionals while providing ...
Quick apply
TSMS - Manager of Process Validation The Technical Services and Manufacturing Sciences (TSMS) Manager of Process Validation will lead and manage a team of technical professionals while providing ...
$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
| 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.
Duties:
Independently understand client's quality standards, cGMP's and regulatory standards to support team in compliance of validation effort. Design validation plans. Conduct independent verification of testing against specifications. Conduct and document impact and risk assessments with a full understanding of equipment/system/ software operation and ability to assess direct, indirect, and no impact systems and functions within complex processes. Complete user interface testing, software verification, and complete alarm testing on automated systems. Develop, review, and execute testing documentation. Make recommendations for design or process modification based on test results when executing test scripts. Work collaboratively with clients' quality representative to complete deviation investigation and resolution for problems and issues encountered during execution activities. Includes ability to complete root cause analysis. Support clients change management program - including author proposed changes, execute impact assessments/ regression analysis and support client documentation of change results and release. Maintain (and ensure the team maintains) clear, detailed records of qualification and validation, and change control activities for future compliance audits.
Requirements:
Bachelor's degree in Mechanical Engineering or related field (or foreign degree equivalent) and at least 5 years of experience in position involving validation engineering. Alternative Requirements: Employer will also accept a Master's degree in Mechanical Engineering or related field (or foreign degree equivalent) and 2 years of experience in position involving validation engineering. Required Skills: Demonstrated ability with lab techniques and general lab analytical operations, and understanding of baseline lab standards and system suitability verification; Demonstrated ability with bench top analytical equipment and chromatography and LIMS system sample workflows; Demonstrated ability with IT system formats, configurations, and workflows; Demonstrated ability with business processes supporting one or more domains, such as: R&D, Clinical, Quality System Management, Supply Chain & Logistics or Commercialization; Demonstrated ability with system design and/or configuration activities; Demonstrated ability with complex automated lab systems such as HPLC, GC, TOC, UV/Vis, Plate Readers and automated titrators; Demonstrated ability with lab system configuration and operation; Demonstrated ability creating various dynamic and static data within a LIMS system; Demonstrated ability with methods and how to acquire, process and report in Empower; Demonstrated ability with system integrations, including how integrations are designed / constructed, data flow from source systems to target systems, typical testing approach for system integrations; Demonstrated ability providing technical guidance and mentorship to other team members; Demonstrated ability identifying areas of business expansion and report to management team for follow-up.
Reports to Verista, Inc. Headquarters in Fishers, Indiana. Telecommuting permissible from home office anywhere in the U.S. Long term placement at unanticipated client sites in the U.S. possible.
Please Send Resumes to: HR Team HR@verista.com
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Pharmaceutical and medicine manufacturing
201 - 500 Employees
Fishers, IN, US
2020