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Computer System Validation Manager Jobs in Alabama

Abbott

Validation Engineer III

Centre, AL · On-site

... computer system validation, spreadsheets, test method validation and process validation. * Writes ... Support the continuous improvement to the Quality Management System, with a specialty focus on ...

CGI Inc.

Senior Computer Systems Analyst

Huntsville, AL · On-site

... data management solutions. This role is essential for ensuring that complex Defense systems ... Support development of coding, testing, debugging, and system validation requirements . Liaise with ...

Southern Research

Senior Validation Analyst

Birmingham, AL · On-site

$108K - $109K/yr

Lead system validation efforts, including validation strategy, risk management approach, and ... Bachelor's degree in computer science or life sciences, other related field, or equivalent ...

Max TC

Computer Operator/Systems Analyst

Huntsville, AL · On-site

... in data management, software engineering, system engineering, test and evaluation support ... We are seeking a full-time Computer Operator/Systems Analyst I to join our team. The System Analyst ...

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All JobsComputer System Validation Manager JobsComputer System Validation Manager Jobs in Alabama

Computer System Validation Manager information

See Alabama salary details

$43.1K

$95.5K

$145.5K

How much do computer system validation manager jobs pay per year?

As of Jun 26, 2026, the average yearly pay for computer system validation manager in Alabama is $95,547.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,500.00 and $119,600.00 per year, depending on experience, location, and employer.

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 popular job titles related to Computer System Validation Manager jobs in Alabama? For Computer System Validation Manager jobs in Alabama, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Manager jobs in Alabama look for? The top searched job categories for Computer System Validation Manager jobs in Alabama are:
What cities in Alabama are hiring for Computer System Validation Manager jobs? Cities in Alabama with the most Computer System Validation Manager job openings:
Computer System Validation Manager jobs near you
Validation Engineer (Aseptic C&Q )

Validation Engineer (Aseptic C&Q )

Centstone

Birmingham, AL • On-site

Contractor

Posted 18 days ago

Job description

Job Title: Validation Engineer (Aseptic C&Q )
Openings: 1
Location: Birmingham, AL (Onsite)
Start: January 2026
Duration: Minimum 6 months (extendable)
Employment Type: Contract

Job Summary
We are seeking a Validation Engineer with strong experience in aseptic pharmaceutical validation and equipment qualification. The ideal candidate will have hands-on expertise in C&Q activities, documentation, and compliance aligned with FDA/EU/GMP standards. This role will support new and existing aseptic facilities and critical manufacturing systems.

Key Responsibilities

  • Develop and maintain validation/qualification documentation for aseptic facilities and equipment.

  • Create and execute C&Q deliverables including URS, risk assessments, commissioning plans, IQ/OQ/PQ protocols, and final reports.

  • Perform Commissioning (COM), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities.

  • Ensure all validation documentation meets internal quality standards and regulatory expectations (FDA/EU/GMP).

  • Conduct risk assessments and define mitigation strategies for aseptic processes and systems.

  • Collaborate cross-functionally with Engineering, Quality, Manufacturing, and other stakeholders to meet project timelines.

  • Support requalification and lifecycle management activities for validated systems and equipment.

  • Lead or support Computer System Validation (CSV) activities, including system classification, test script creation/execution, and compliance reporting.

  • Verify system functionality and data integrity consistent with regulatory requirements.

Required Qualifications

  • Bachelor’s degree in Engineering or Science (preferred).

  • 3–5 years of experience in validation/qualification of aseptic pharmaceutical processes and/or equipment.

  • Strong knowledge of FDA/EU regulatory frameworks, GMPs, and industry best practices.

  • Demonstrated experience authoring and executing URS, protocols, and validation reports.

  • Strong understanding of pharmaceutical manufacturing equipment and process validation.

  • Proficiency with documentation tools and Microsoft Office (Word, Excel, PowerPoint).

  • Excellent communication, organization, and stakeholder management skills.

  • Ability to work independently and within cross-functional teams.

Preferred/Tools & Equipment Exposure

  • Experience with Kaye Validator AVS and ValProbe systems.

  • Knowledge of qualification for equipment such as:

    • Homogenizers

    • Pump skids

    • SIP/CIP skids

    • Temperature control units (CTUs)

    • Tanks and related utilities

  • Experience supporting aseptic facility start-ups, expansions, or technology transfers.

Thanks & Regards,

Adarsh Mallik | IT Recruiter
adarsh.mallik@centstone.com
CENTSTONE SERVICES
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About Centstone

Sourced by ZipRecruiter

In the dynamic landscape of today’s business environment, flexibility is key. At Centstone, we understand the unique demands of your industry and offer tailored Contract Hiring solutions to empower your organization with the right talent when you need it most.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Hazlet, NJ, US

Year founded

2022

Social media

Facebook

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