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Computer System Validation Manager Jobs in New Hampshire

Coordinate MES patching, upgrades, and system validation testing in accordance with change control ... Bachelor's degree in Computer Science, Information Technology, a related field, or equivalent ...

Coordinate MES patching, upgrades, and system validation testing in accordance with change control ... Bachelor's degree in Computer Science, Information Technology, a related field, or equivalent ...

Coordinate MES patching, upgrades, and system validation testing in accordance with change control ... Associate's degree in Computer Science, Information Technology, a related field, or equivalent ...

Coordinate MES patching, upgrades, and system validation testing in accordance with change control ... Associate's degree in Computer Science, Information Technology, a related field, or equivalent ...

Mercury Systems uses cutting edge technology from Intel, Freescale, Xilinx, Altera, Broadcom, and ... Experience for technical management of third party CAD engineering. * Self-motivated - candidate ...

Mercury Systems uses cutting edge technology from Intel, Freescale, Xilinx, Altera, Broadcom, and ... Experience for technical management of third party CAD engineering. * Self-motivated - candidate ...

Showing results 41-60

Computer System Validation Manager information

What does a computer system validation manager do?

A Computer System Validation Manager is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards. They oversee the planning, execution, and documentation of validation activities to ensure systems are reliable, accurate, and secure. Their duties include managing validation projects, writing protocols, coordinating with IT and quality assurance teams, and ensuring adherence to regulations like FDA 21 CFR Part 11. This role is critical for maintaining product quality and regulatory compliance.

What are the key skills and qualifications needed to thrive as a computer system validation manager, and why are they important?

To thrive as a Computer System Validation Manager, you need expertise in computer system validation regulations (such as GxP, FDA 21 CFR Part 11), strong project management skills, and a background in life sciences or IT. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and compliance software is often required, along with relevant certifications like PMP or CSV-related credentials. Exceptional attention to detail, analytical thinking, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to ensure validated systems meet regulatory standards, minimize compliance risks, and support organizational quality objectives.

What are some common challenges a computer system validation manager faces during system implementation projects?

A Computer System Validation Manager often encounters challenges such as aligning validation activities with evolving regulatory requirements, managing tight project timelines, and coordinating between multiple stakeholders like IT, Quality Assurance, and business users. Ensuring thorough documentation and traceability, while adapting to technology updates or scope changes, can also be demanding. Proactive communication and strong project management skills are essential to mitigate risks and ensure successful, compliant system implementations.

What is the difference between Computer System Validation Manager vs Computer System Validation Specialist?

AspectComputer System Validation ManagerComputer System Validation Specialist
CertificationsGAMP, CQE, CSQEGAMP, CQE, CSQE
Work EnvironmentManagement, oversight, strategic planningExecution, testing, documentation
Industry UsagePharmaceutical, biotech, regulated industriesPharmaceutical, biotech, regulated industries
Primary FocusLeading validation projects, team coordinationPerforming validation activities, testing

The main difference between a Computer System Validation Manager and a Computer System Validation Specialist lies in their roles. The manager oversees validation projects, manages teams, and ensures compliance, while the specialist executes validation tasks and documents testing procedures. Both roles require similar certifications and are vital in regulated industries like pharmaceuticals and biotech.

What are the most commonly searched types of Computer System Validation jobs in New Hampshire?

The most popular types of Computer System Validation jobs in New Hampshire are:

What are popular job titles related to Computer System Validation Manager jobs in New Hampshire?

For Computer System Validation Manager jobs in New Hampshire, the most frequently searched job titles are:

What job categories do people searching Computer System Validation Manager jobs in New Hampshire look for?

The top searched job categories for Computer System Validation Manager jobs in New Hampshire are:

What cities in New Hampshire are hiring for Computer System Validation Manager jobs?

Cities in New Hampshire with the most Computer System Validation Manager job openings:

Infographic showing various Computer System Validation Manager job openings in New Hampshire as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution.

Systems Engineer, Level 3

Lonza

Portsmouth, NH • On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 7 days ago


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical


Job description

System Engineer, Level 3

Location: On-site, Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.

The Systems Engineer will support ongoing Lonza operations through technical assistance as it relates to computerized systems infrastructure for process automation and QC laboratory systems. This person provides a technical resource to operations customers to ensure that systems are designed and operating to meet production needs.

What you will get:

  • An agile career and dynamic working culture.

  • An inclusive and ethical workplace.

  • Competitive salary and performance-based bonuses

  • 401(k) matching plan.

  • Competitive compensation programs that reward high performance.

  • Comprehensive medical, dental, and vision insurance.

Access to our full list of global benefits: https://www.lonza.com/careers/benefits

What you will do:

  • Administer, monitor, and maintain manufacturing execution systems using Emerson Syncade (or equivalent such as Lonza MODA-ES and RockwellPharma Suite) including application servers, web servers, system interfaces, and other integration points.
  • Support batch record execution, electronic work instructions, and material tracking performance within the MES environments.
  • Coordinate MES patching, upgrades, and system validation testing in accordance with change control procedures.
  • Serve as primary technical point of contact for MES-related system incidents, working closely with production, automation engineering teams, and quality to minimize downtime.
  • Support connectivity between MES, DCS, analytical systems, and PLC platforms (Rockwell/Allen, Siemens) via Kepware, OPC Router, or similar middleware.
  • Troubleshoot data flow, perform ad-hoc queries, manage vendor tickets, lead root cause analysis, and provide 24/7 on-call support.
  • Maintain IT and regulatory compliance, update system documentation, and collaborate on site and global projects.

What we are looking for:

  • Bachelor's degree in Computer Science, Information Technology, a related field, or equivalent practical experience with minimum of 3-5 years of experience in systems administration or network engineering.
  • 3+ years of experience administering Windows Server environments, Active Directory, and SQL Server.
  • A strong proficiency in Microsoft Windows Server administration, including hands-on experience with Active Directory and related Windows services and an understanding of virtualization technologies such as VMware or HyperV.
  • Experience administering platforms like Emerson Syncade and data historians like OSIsoft PI.
  • Proficiency in PowerShell and Visual Basic for automation and troubleshooting. Knowledge of Kepware, FactoryTalk, OPC Router, and DCOM/OPC configurations.
  • Background in validated GxP environments, change control, and relevant technical certifications.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.


What Lonza employees say

Pay

Benefits

Hours and flexibility

Workplace

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US