Automation Validation Lead
Andover, MA · On-site +1
Automation Validation Lead Location : Andover, MA Duration - 6 months (possible extension ... Ethernet Profibus OPC The ideal candidate should be familiar with the following computer system ...
Andover, MA · On-site +1
Automation Validation Lead Location : Andover, MA Duration - 6 months (possible extension ... Ethernet Profibus OPC The ideal candidate should be familiar with the following computer system ...
Andover, MA · On-site +1
Automation Validation Lead Location : Andover, MA Duration - 6 months (possible extension ... Ethernet Profibus OPC The ideal candidate should be familiar with the following computer system ...
Bedford, NH · On-site
$120 - $160/hr
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Bedford, NH · On-site
$120 - $160/hr
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Bedford, NH · On-site
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Bedford, NH · On-site
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Bedford, NH · On-site
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Bedford, NH · On-site
The scope of responsibility encompasses all planning and implementation of drug and medical device overall validation activities, including computer systems, in a CMO aseptic fill finish environment ...
Andover, MA · On-site
... computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures. Candidate requires strong interpersonal, oral and written communication skills as ...
Andover, MA · On-site
... computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures. Candidate requires strong interpersonal, oral and written communication skills as ...
Andover, MA · On-site
$30/hr
Subject matter expert (SME) for all major site infrastructure systems e.g. Compressed Air, Gases ... Validation within a pharmaceutical manufacturing environment. 3.In depth understanding of Site ...
Andover, MA · On-site
$30/hr
Subject matter expert (SME) for all major site infrastructure systems e.g. Compressed Air, Gases ... Validation within a pharmaceutical manufacturing environment. 3.In depth understanding of Site ...
Pepperell, MA · On-site
$43.27 - $53.49/hr
Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer will ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...
Pepperell, MA · On-site
$43.27 - $53.49/hr
Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer will ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...
Bedford, NH · On-site
Perform a periodic review of systems to monitor the validation status of the system as well as write and develop validation SOPs. * Help define validation strategies based on regulations, guidance ...
Bedford, NH · On-site
Perform a periodic review of systems to monitor the validation status of the system as well as write and develop validation SOPs. * Help define validation strategies based on regulations, guidance ...
Bedford, NH · On-site
Perform a periodic review of systems to monitor the validation status of the system as well as write and develop validation SOPs. * Help define validation strategies based on regulations, guidance ...
Bedford, NH · On-site
Perform a periodic review of systems to monitor the validation status of the system as well as write and develop validation SOPs. * Help define validation strategies based on regulations, guidance ...
Working knowledge of Computer System Validation and Change Control requirements. * Assist is leading large or cross-functional projects and improvement initiatives as assigned. Preferred: * Superior ...
Working knowledge of Computer System Validation and Change Control requirements. * Assist is leading large or cross-functional projects and improvement initiatives as assigned. Preferred: * Superior ...
Working knowledge of Computer System Validation and Change Control requirements. * Assist is leading large or cross-functional projects and improvement initiatives as assigned. Preferred: * Superior ...
Working knowledge of Computer System Validation and Change Control requirements. * Assist is leading large or cross-functional projects and improvement initiatives as assigned. Preferred: * Superior ...
Andover, MA · On-site
$120 - $150/hr
Draeger Medical Systems, Inc., Job-ID: 1328 * Location: Andover * Function: R&D * Work Location ... Perform product validation planning and providing feedback to the cross-functional team on customer ...
New
Andover, MA · On-site
$120 - $150/hr
Draeger Medical Systems, Inc., Job-ID: 1328 * Location: Andover * Function: R&D * Work Location ... Perform product validation planning and providing feedback to the cross-functional team on customer ...
New
Andover, MA · On-site
$122 - $149/hr
Draeger Medical Systems, Inc., Job-ID: 1328 * Location: Andover * Function: R&D * Work Location ... Perform product validation planning and providing feedback to the cross-functional team on customer ...
New
Andover, MA · On-site
$122 - $149/hr
Draeger Medical Systems, Inc., Job-ID: 1328 * Location: Andover * Function: R&D * Work Location ... Perform product validation planning and providing feedback to the cross-functional team on customer ...
New
Exeter, NH · On-site
$22 - $29.61/hr
For patients whose lab tests have already been ordered in a BILH computer system, validate and/or update the patient's demographic and information in a BILH computer system, and, for other patients ...
Exeter, NH · On-site
$22 - $29.61/hr
For patients whose lab tests have already been ordered in a BILH computer system, validate and/or update the patient's demographic and information in a BILH computer system, and, for other patients ...
$43.27 - $53.49/hr
Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer - CQV ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...
New
$43.27 - $53.49/hr
Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer - CQV ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...
New
Exeter, NH · On-site
$18.50 - $22.25/hr
Responsibilities: • Provide excellent phlebotomy and phlebotomy-related services for all patients. • For patients whose lab tests have already been ordered in a BILH computer system, validate and ...
Exeter, NH · On-site
$18.50 - $22.25/hr
Responsibilities: • Provide excellent phlebotomy and phlebotomy-related services for all patients. • For patients whose lab tests have already been ordered in a BILH computer system, validate and ...
Pepperell, MA · On-site
$43.27 - $53.49/hr
Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer - CQV ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...
Pepperell, MA · On-site
$43.27 - $53.49/hr
Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer - CQV ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...
MA · On-site
$43.27 - $53.49/hr
Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer - CQV ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...
MA · On-site
$43.27 - $53.49/hr
Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer - CQV ... Spreadsheet and word processing applications experience, computer literacy. * Strong written and ...
At DEKA you can! How you will make an impact as a Verification & Validation Test Engineer ... Must have fluid system handling experience * Leadership and/or mentoring experience * Knowledge and ...
At DEKA you can! How you will make an impact as a Verification & Validation Test Engineer ... Must have fluid system handling experience * Leadership and/or mentoring experience * Knowledge and ...
How you will make an impact as a Verification & Validation Test Engineer: * Writing test plans ... Must have fluid system handling experience * Leadership and/or mentoring experience * Knowledge and ...
Quick apply
How you will make an impact as a Verification & Validation Test Engineer: * Writing test plans ... Must have fluid system handling experience * Leadership and/or mentoring experience * Knowledge and ...
$10.32 - $17.01
2% of jobs
$17.01 - $23.70
9% of jobs
$23.70 - $30.39
1% of jobs
$30.39 - $37.09
4% of jobs
$41.15 is the 25th percentile. Wages below this are outliers.
$37.09 - $43.78
15% of jobs
$43.78 - $50.47
9% of jobs
The median wage is $56.05 / hr.
$50.47 - $57.16
13% of jobs
$62.49 is the 75th percentile. Wages above this are outliers.
$57.16 - $63.86
29% of jobs
$63.86 - $70.55
12% of jobs
$70.55 - $77.24
2% of jobs
$77.24 - $83.94
5% of jobs
$10
$52
$83
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.
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.
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.
The most popular types of Computer System Validation jobs in Manchester, NH are:
For Computer System Validation jobs in Manchester, NH, the most frequently searched job titles are:
The top searched job categories for Computer System Validation jobs in Manchester, NH are:

Emvia Inc
Position : Automation Validation Lead
Location : Andover, MA
Duration - 6 months (possible extension)
Interview mode- Local or regional candidates preferred. May be open to Skype for excellent candidate.
Job description:
The Automation Validation Lead is responsible for overseeing all automation testing (leveraged software Factory Acceptance Tests, Commissioning and Validation) to ensure successful validation of all automation systems
The Automation Validation Lead will report to the Automation Lead and additionally take direction from the Projects Validation Lead. The Automation Validation Lead will be an active member of the overall project team working with the team, Engineer of Record and Construction Manager.
Key Responsibilities:
Finalize the Automation Validation Plan
Work with a team of Engineers and System Integration (SI) contractors to complete all validation deliverables related to the Delta-V Manufacturing Control System (MCS) and Qualified Utilities Network (QUN)
Give guidance on validation best practices for automation hardware, software and computer systems.
Follow FDA Title 21 CFR Part 11 for Data Integrity Compliance
Draft, review or approve automation design and testing documents for all phases of testing (sFAT, Commissioning, Validation)
Drive deviation resolution for all testing
Requirements:
7 years of relevant automation validation experience
The candidate must have a strong background working in cGMP environments.
The candidate must have excellent communication skills.
Experience with Emerson Controllers and Emerson DeltaV Software is required.
The ideal candidate would have experience with the following hardware: Allen Bradley PLCs and I/O
o The ideal candidate would have experience with the following software: GEs Proficy FIX, OSISofts OSIPi or similar Historian software Reporting software, InfoBatch is preferred
The ideal candidate should be familiar with the following communication methods/protocols: Ethernet Profibus OPC
The ideal candidate should be familiar with the following computer system software and hardware: Windows operating systems Windows Terminal Services/Remote Desktop VMWare Dell VRTX familiarity is a plus
Limited local travel to software Factory Acceptance Tests (FATs) may be required
Work Location: Andover, MA
Over time may be required during peak times but the expectation is that the it will typically be a standard 40 hour work week.
All your information will be kept confidential according to EEO guidelines.
Sourced by ZipRecruiter
Software development
11 - 50 Employees
Allen, TX, US
2007