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Computer System Validation Manager Jobs in New Hampshire

Lonza

Operations Technology Manager

Portsmouth, NH · On-site

Enforce strict adherence to cGMP regulations, data integrity, and system validation. * Team ... Bachelor's of Science Engineering (Computer Science, IT or related field Engineering, Computer ...

Lonza

Operations Technology Manager

Portsmouth, NH · On-site

Enforce strict adherence to cGMP regulations, data integrity, and system validation. * Team ... Bachelor's of Science Engineering (Computer Science,ITor related field Engineering, Computer ...

Lonza

Systems Engineer, Level 3

Portsmouth, NH · On-site

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 ...

Lonza

Systems Engineer, Level 3

Portsmouth, NH · On-site

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 ...

Lonza

Systems Development Engineer II

Portsmouth, NH · On-site

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 ...

Lonza

Systems Development Engineer II

Portsmouth, NH · On-site

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 ...

Socket.dev

Principal Systems Test Engineer

Bedford, NH · On-site

$140 - $190/hr

... system validation. This role involves defining test strategies, managing direct reports, and ... Bachelor's degree in Computer Science, Engineering, or a related field * 10+ years of experience in ...

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Computer System Validation Manager information

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 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 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:
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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:
Computer System Validation Manager jobs near you
Infographic showing various Computer System Validation Manager job openings in New Hampshire as of August 2026, with employment types broken down into 77% Full Time, 9% Part Time, and 14% Contract. Highlights an 86% In-person, 5% Hybrid, and 9% Remote job distribution.

Senior IT Manager

Life Science Outsourcing, Inc

Somersworth, NH • On-site

$131K - $131K/yr

Other

Posted 12 days ago

Job description

Lead the Technology Behind Life-Saving Medical Devices
At Life Science Outsourcing (LSO), the systems you manage do more than keep a business running. They keep a regulated medical device manufacturer producing products that reach real patients. As our Senior IT Manager, you will own information technology across our California and New Hampshire facilities, combining strategic planning with hands-on technical depth to deliver secure, reliable, and compliant technology operations.
This role suits a leader who is equally comfortable setting a technology roadmap with executives and rolling up their sleeves on infrastructure, cybersecurity, and ERP. LSO runs a co-managed IT model: you supervise our internal L1 support specialist, personally own L2 escalations, and direct a back-end L3 engineering MSP. If you want real, hands-on ownership of the full IT function in a regulated manufacturing environment, this is that seat.
What You'll Do
Reporting to the Chief Financial Officer, you will lead all aspects of IT for approximately 220 employees across two manufacturing sites.
Strategy and Leadership
  • Develop and execute LSO's IT strategy and technology roadmap in partnership with executive leadership.
  • Manage IT budgets, vendors, software licensing, contracts, and managed service providers.
  • Lead enterprise AI adoption and governance, collaborating with our parent company's AI initiatives.

Infrastructure and Operations
  • Administer Microsoft 365, Azure, Entra ID, Active Directory, Windows Server, virtualization, networking, and endpoint management.
  • Ensure high availability through monitoring, backup, disaster recovery, and business continuity planning.
  • Serve as the L2 escalation tier, providing hands-on troubleshooting across Microsoft 365 and Entra, endpoints, servers, networking, Deacom, and production applications.

Cybersecurity and Compliance
  • Lead cybersecurity initiatives supporting NIST 800-171, ISO 13485, FDA, and customer requirements.
  • Maintain IT governance, policies, documentation, and audit readiness.
  • Support 21 CFR Part 11 compliance and data integrity for electronic records in our quality system.

ERP and Business Applications
  • Serve as the primary IT owner of our Deacom ERP environment and related manufacturing applications.
  • Drive reporting, automation, and continuous process improvement across business systems.

Team and Vendor Management
  • Supervise and develop our L1 IT Support Specialist (first-touch support, onboarding, equipment, routine requests), providing L1 coverage when needed, including remote supervision.
  • Direct our co-managed L3 engineering MSP: you own every escalation as the internal point of contact and work directly with the MSP on resolution; the MSP does not support end users.
  • Retain internal ownership of Deacom application support, OT and production systems, physical-access systems, and backup and disaster recovery.

What You Bring
Skills & Experience
  • Bachelor's degree in Information Technology, Computer Science, or a related field, or equivalent experience.
  • 7+ years of progressively responsible IT experience, including 3+ years managing IT operations, projects, or technical teams.
  • Strong experience with Microsoft 365, Azure, Entra ID, Active Directory, Windows Server, networking, virtualization, and endpoint management.
  • Experience with cybersecurity frameworks such as NIST, ISO, or SOC, plus PowerShell scripting and automation.
  • Experience supporting ERP systems in a manufacturing environment; familiarity with 21 CFR Part 11 and computer system validation principles is a strong plus.

Mindset & Impact
  • An owner's mentality: you treat uptime, security, and data integrity as personal commitments.
  • Comfort operating at two altitudes, presenting a roadmap to executives in the morning and troubleshooting infrastructure in the afternoon.
  • Calm, structured judgment during incidents, audits, and inspections.
  • A collaborative style that builds trust with Operations, Quality, Finance, and site leadership across two locations.
Compensation
The expected pay range for this position is dependent on experience, qualifications, primary work location, and internal equity. LSO reviews compensation regularly and offers competitive pay aligned with market benchmarks for the Brea, California and Somersworth, New Hampshire areas.
Why Join LSO?
  • Your work directly supports life-saving medical devices used by real patients.
  • Full ownership of the IT function with direct access to executive leadership.
  • A regulated industry environment that builds rare, career-defining compliance and systems expertise.
  • Two-site scope with modern cloud infrastructure and an active AI enablement agenda.
  • A collaborative, hands-on culture where your decisions are visible on the production floor.
Work Environment
  • Hybrid work arrangement based at either our Brea, CA or Somersworth, NH facility.
  • Periodic travel between sites (approximately 4 to 6 trips annually).
  • Participation in after-hours support for critical production or infrastructure incidents.
  • Primarily office-based work with occasional presence in production, cleanroom, warehouse, and server areas subject to facility PPE and gowning requirements.
  • FDA 21 CFR Part 820 and ISO 13485 regulated manufacturing environment.
Make an Impact
Every system you secure, every audit you pass, and every hour of uptime you protect helps LSO deliver medical devices that clinicians and patients depend on. This is a role where technology leadership translates directly into patient impact. If you are ready to own IT for a growing, regulated manufacturer, we want to meet you.

Apply