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Contract Validation Engineer Jobs in Alabama (NOW HIRING)

Abbott

Validation Engineer III

Centre, AL · On-site

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 ...

AeroVironment

Contracts Manager

Huntsville, AL

$87K - $117K/yr

... and engineering, to streamline contract workflows and mitigate risks. Your expertise will be ... Oversee maintenance and retrieval of contract documents/files and validated data, preparation of ...

AeroVironment

Contracts Manager

Huntsville, AL · Hybrid

$87K - $117K/yr

... and engineering, to streamline contract workflows and mitigate risks. Your expertise will be ... Oversee maintenance and retrieval of contract documents/files and validated data, preparation of ...

Ag

Manufacturing Engineer A220 (Contract)

Mobile, AL

$72K - $93K/yr

... Engineer I A220 (Contract) to join our Final Assembly Line based in Mobile, AL. Responsible for ... This position will also be responsible to validate workbook modification, assist with tooling ...

DCS CORPORATION

Contracts Analyst

Huntsville, AL · On-site

$64K - $77K/yr

In this role, you will draft complete Contract Requirements Packages (CRPs) for weapon system ... engineering services contracts for high-dollar efforts. The successful candidate will be highly ...

DCS Corporation

Contracts Analyst

Huntsville, AL · On-site

$64K - $77K/yr

In this role, you will draft complete Contract Requirements Packages (CRPs) for weapon system ... engineering services contracts for high-dollar efforts. The successful candidate will be highly ...

DCS Corp

Contracts Analyst

Huntsville, AL

$68K - $82K/yr

In this role, you will draft complete Contract Requirements Packages (CRPs) for weapon system ... engineering services contracts for high-dollar efforts. The successful candidate will be highly ...

deciBel Research, Inc.

Systems Engineer

Huntsville, AL · On-site

... validation plans, interface specifications, etc.) are maintained, applied, and continuously ... Prior involvement in development and production of technical Contract Data Requirements List (CDRL ...

Benchmark

Quality Engineer II

Huntsville, AL · On-site

$70K - $91K/yr

... validation and certification of routine technical manuals required by the contract * Maintain ... in engineering design and delivering world-class manufacturing services for products that make a ...

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How much do contract validation engineer jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for contract 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 are the primary responsibilities of a Contract Validation Engineer on a typical project?

A Contract Validation Engineer is primarily responsible for reviewing and verifying that project deliverables, processes, and products comply with contractual requirements and industry standards. This includes conducting thorough documentation reviews, performing technical validations, and collaborating with project managers, legal teams, and quality assurance professionals to resolve any discrepancies. You will also support audits, maintain compliance records, and participate in meetings to ensure all stakeholders remain informed and aligned. The role often involves both independent analysis and teamwork, providing an excellent environment for those who enjoy balancing technical expertise with cross-functional collaboration.

What are the key skills and qualifications needed to thrive in the Contract Validation Engineer position, and why are they important?

To thrive as a Contract Validation Engineer, you need strong analytical skills, a degree in engineering or a related field, and a deep understanding of contract requirements and industry regulations. Proficiency with validation software, quality management systems (QMS), and relevant certifications such as Six Sigma or ISO standards is often preferred. Outstanding attention to detail, effective communication, and the ability to work collaboratively across departments are crucial soft skills. These competencies ensure accurate contract assessments, regulatory compliance, and seamless integration of contractual obligations into engineering projects.

What is a Contract Validation Engineer job?

A Contract Validation Engineer is responsible for ensuring that systems, processes, and products meet regulatory and contractual requirements. They typically work on a temporary or project basis, verifying compliance through testing, documentation, and analysis. Their role involves collaborating with engineering teams to validate designs, troubleshoot issues, and ensure quality standards are met. This position is common in industries like pharmaceuticals, aerospace, and manufacturing, where strict validation protocols are required.

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 Contract Validation Engineer jobs in Alabama? For Contract Validation Engineer jobs in Alabama, the most frequently searched job titles are:
What job categories do people searching Contract Validation Engineer jobs in Alabama look for? The top searched job categories for Contract Validation Engineer jobs in Alabama are:
What cities in Alabama are hiring for Contract Validation Engineer jobs? Cities in Alabama with the most Contract Validation Engineer job openings:
Contract Validation Engineer jobs near you
Validation Engineer III

Validation Engineer III

Abbott

Centre, AL • On-site

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 23 days ago

Abbott rating

7.9

Company rating: 7.9 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

156th of 528 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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