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Validation Engineer 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- Contract Abbott Rapid Diagnostics (formerly Alere) is part of Abbott's Diagnostics family of ...

CAI

Senior Validation Engineer

Huntsville, AL

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Huntsville, AL · On-site

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Huntsville, AL · On-site

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

IGNITE

FLIGHT SCIENCES ENGINEER

Huntsville, AL · On-site

... validated engineering solutions. • Plan and execute dynamic and static test campaigns-including separation events-then synthesize results into clear, data-driven insights that influence design ...

Adtran

Manufacturing Engineering Specialist

Huntsville, AL · On-site

$68K - $87K/yr

Develop, validate, and maintain back-end manufacturing processes , including: * Press-fit insertion ... Lead manufacturing engineering activities during NPI builds and product launches * Review and ...

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How much do validation engineer jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for validation engineer in Alabama is $47.13, according to ZipRecruiter salary data. Most workers in this role earn between $35.72 and $57.31 per hour, depending on experience, location, and employer.

What Is a Validation Engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

What is the difference between Validation Engineer vs Quality Assurance Engineer?

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

What are the key skills and qualifications needed to thrive as a Validation Engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges Validation Engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

What are Validation Engineers?

Validation Engineers are professionals responsible for ensuring that systems, processes, or equipment meet regulatory standards and function as intended. They typically work in industries such as pharmaceuticals, biotechnology, manufacturing, and medical devices. Their duties involve creating validation protocols, conducting tests, analyzing data, and documenting results to ensure compliance with industry regulations and quality standards. Validation Engineers play a critical role in maintaining product safety and efficacy, as well as helping companies pass audits and inspections.
More about Validation Engineer jobs
What are the most commonly searched types of Validation Engineer jobs in Alabama? The most popular types of Validation Engineer jobs in Alabama are:
What are popular job titles related to Validation Engineer jobs in Alabama? For Validation Engineer jobs in Alabama, the most frequently searched job titles are:
What job categories do people searching Validation Engineer jobs in Alabama look for? The top searched job categories for Validation Engineer jobs in Alabama are:
What cities in Alabama are hiring for Validation Engineer jobs? Cities in Alabama with the most Validation Engineer job openings:
What are popular job titles related to Validation Engineer jobs in AL? For Validation Engineer jobs in AL, the most frequently searched job titles are:
Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Alabama as of June 2026, with employment types broken down into 81% Full Time, 15% Part Time, 2% Temporary, and 2% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $98,028 per year, or $47.1 per hour.

Validation Engineer III

Abbott

Centre, AL • On-site

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 5 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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