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Computer Validation Jobs in Alabama (NOW HIRING)

Abbott

Validation Engineer III

Centre, AL · On-site

Validation Engineer III Location: San Diego, CA Duration: 7 Month Assignment Validation Engineer ... Working experience with GAMP5 and FDA's Computer Software Assurance initiatives * Working ...

Southern Research

Senior Validation Analyst

Birmingham, AL · On-site

$108K - $109K/yr

Senior Validation Analyst Southern Research + You Discover a career where your work truly matters ... Bachelor's degree in computer science or life sciences, other related field, or equivalent ...

BC Tech Pro

Computer Field Technician

Madison, AL

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Madison, AL · On-site

$35/hr

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Mobile, AL

$35/hr

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Homewood, AL · On-site

$35/hr

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Homewood, AL

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Mcintosh, AL

$35/hr

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Mcintosh, AL · On-site

$35/hr

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Montgomery, AL · On-site

$35/hr

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Montgomery, AL

$35/hr

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Homewood, AL

$35/hr

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

BC Tech Pro

Computer Field Technician

Madison, AL

$35/hr

You must have a reliable form of transportation and a valid driver's license to run these calls. You will be visiting multiple work sites throughout your day. * You must have access to a computer and ...

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Computer Validation information

See Alabama salary details

$9

$49

$78

How much do computer validation jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for computer validation in Alabama is $49.23, according to ZipRecruiter salary data. Most workers in this role earn between $37.93 and $58.41 per hour, depending on experience, location, and employer.

Can computer engineers make $500,000?

Computer validation professionals typically do not earn $500,000 annually, as this level of compensation is uncommon in the field. High salaries may be possible for senior roles, especially in biotech or pharmaceutical industries, or with extensive experience, specialized skills, and leadership responsibilities. Most salaries for computer validation roles range from $70,000 to $150,000 per year.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

What is the salary of a CSV engineer?

A CSV (Computer System Validation) engineer's salary typically ranges from $70,000 to $120,000 annually, depending on experience, location, and certifications. Senior roles or those with specialized skills in validation tools and regulatory compliance may earn higher salaries.

Is computer system validation a good field?

Computer validation professionals ensure that computer systems in regulated industries meet quality and compliance standards, often working with tools like GxP and validation protocols. The field offers steady demand, especially in pharmaceuticals and biotech, and requires knowledge of regulatory requirements and validation processes. It can be a rewarding career for those interested in quality assurance, compliance, and technical problem-solving.

Is CSV a skill?

In the context of computer validation, familiarity with CSV (comma-separated values) files is considered a useful technical skill, as it involves working with data formats and data management tools. Proficiency in handling CSV files can support tasks such as data import/export, validation, and reporting. However, CSV itself is a data format, not a standalone skill, but understanding how to work with it is valuable for validation professionals.
What are popular job titles related to Computer Validation jobs in Alabama? For Computer Validation jobs in Alabama, the most frequently searched job titles are:
What job categories do people searching Computer Validation jobs in Alabama look for? The top searched job categories for Computer Validation jobs in Alabama are:
Computer Validation jobs near you

Validation Engineer III

Abbott

Centre, AL • On-site

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 9 hours ago

Abbott rating

7.9

Company rating: 7.9 out of 10

Based on 132 frontline employees who took The Breakroom Quiz

149th of 520 rated manufacturers

Job description

Title: Validation Engineer III
Location: San Diego, CA
Duration: 7 Month Assignment
Validation Engineer- Contract
Abbott Rapid Diagnostics (formerly Alere) is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. At Abbott, diverse ideas, perspectives, and expertise allow us to create life-changing solutions that help people live healthier lives. In 150 countries and with businesses spanning nutrition, diagnostics, medical devices, and branded generic pharmaceuticals, Abbott offers you enormous opportunities to explore your interests and help you achieve your career and personal goals.
Abbott is looking for an outstanding Validation Engineer-Contractor who will effectively lead quality related validation activities to support the Quality Management System. The end goal is to deliver consistent and high-quality validation and supporting documentation for design and development organization. This role requires strong technical, communication, interpersonal and organizational skills, and a solid understanding of the application of FDA, ISO 13485, ISO 14971 standards and company strategies.
This opportunity is available with Infectious Disease Developed Markets (IDDM) Business unit within Abbott, at our location in Towne Centre San Diego, CA.
This job description will be reviewed periodically and is subject to change by management.
Technical Writing
  • Write procedures, investigations, protocols, deviations, CAPA's, reports, change controls, etc. to support ARDx Towne Centre site departments.
  • Perform and document investigations related to validation activities and performs risk assessments of equipment, processes and systems to determine the scope of validation efforts.
  • Generates validation documentation as required (URS, FRS, DRS, FAT, DQ, engineering studies, IOQ, PQ, PV) for cleaning, shipping, sterilization, facilities,
  • utilities, systems, equipment qualification/requalification, computer system validation, spreadsheets, test method validation and process validation.
  • Writes and/or revises IQ, OQ, PQ related documents, including any or all of the following: SOP's, validation master plans, guidelines and execution plans, automation test plans and technical documents.
  • Responsible for writing Standard Operating Procedures related to Validations and responsible for training Quality Assurance and R&D personal in the validation processes.

Service Delivery
  • Performs on site or support work, including but not limited to:
  • Validation protocol executions for FAT/SAT/IQ/OQ/PQ/PV.
  • Equipment Qualification test execution.
  • Investigations and deviations.
  • Provides gap analysis, risk management, risk assessment, risk analysis and validation strategy.
  • Data integrity assessments and review of client data
  • Executes protocols and resolves deviations/discrepancies, analyzes data and writes reports.
  • Performing and supervising thermal mapping of temperature-controlled units, Laboratories, warehouses, etc.
  • Ensures that validations are documented using Good Documentation Practices and are in compliance to FDA, ISO 13485, and Abbott Policies and Procedures.
  • Evaluate impact on legacy qualifications/validations and determines the scope of re-validation.
  • Support the continuous improvement to the Quality Management System, with a specialty focus on validation processes.
  • Responsible for maintaining a Site Master Validation Plan and ensuring that critical Performance Qualification and/or Process Validations are performed per established schedule.
  • Identify and propose remediation for existing and potential validation issues; provide technical expertise and provide solutions to maintain compliance.
  • Assist with internal and external audits.
  • Manages validation metrics.
  • Manages change control for validation deliverables in the electronic documentation management system.
  • Participate in multiple, concurrent projects.
  • Develops timelines and tracks project status on assigned projects.
  • Keeps stakeholders informed on the status of important projects.
  • Performs other duties as assigned by Management.

BASIC QUALIFICATIONS | EDUCATION:
  • Bachelors' degree (B.S.) in a Science related field (Engineering, Biology, Chemistry or equivalent)
  • 5+ years of related work experience in a medical device industry with strong technical competency in performing equipment qualification (IQ/OQ/PQ), facility/lab qualification, process validations and excel spreadsheet validations.
  • Proficient understanding of Design Control, Good Documentation Practices (GDP), and current Good Manufacturing Practices (cGMP)
  • Significant experience with application of the FDA regulations and recognized standards (e.g., FDA 21 CFR 820.30, FDA 21 CFR 820.70, FDA 21 CFR Part 11, ISO 13485, ISO 14971, cybersecurity)

PREFERRED QUALIFICATIONS:
  • Experience in validation of In Vitro Diagnostic Lab equipment (e.g., Real- Time PCR System, Freezers, Refrigerators, Environmental Chambers, Incubators) and Thermal Mapping, Computerized System Validation.
  • Experience supporting ISO 13485 inspections and FDA inspections.• Experience in a multi-site development environment.
  • Experience in compliance management within a rapid-growth, dynamic organization.
  • Statistical or Lean Six Sigma background
  • Working experience with GAMP5 and FDA's Computer Software Assurance initiatives
  • Working experience with Agile, Maximo and ViewLinc.

COMPETENCIES:
  • Good working knowledge of Excel and Microsoft Word software
  • Working knowledge of quality techniques such as root cause analysis, 5 why's, and Ishikawa diagrams.
  • Excellent problem solving and decision-making skills.
  • Self-starting, detail oriented, and ability to focus on task at hand
  • Initiative to work towards goals with minimal supervision
  • Ability to work independently with multiple departments to resolve Validation issues
  • Must be able to work effectively in a fast paced, cross-functional team-oriented environment
  • Well-developed English written and verbal communication skills

An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.We provide reasonable accommodation to qualified individuals with disabilities.
Consultants Eligible Benefits Upon Waiting Period:
  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account (for High-Deductible Health Plans)
  • Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
  • Supplemental Life Insurance
  • Short Term Disability (coverage varies by state)
  • Long Term Disability
  • Critical Illness, Hospital coverage, Accident Insurance
  • MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
  • 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
  • Published on 27 May 2026, 1:56 PM

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