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Contract Cleaning Validation Engineer Jobs in Alabama

... cleaning validation planning and execution, piping and instrumentation diagrams (P&ID), chemical process engineering and pharmaceutical process development • Working knowledge of FDA regulations ...

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 ...

International Contracts Manager

Huntsville, AL · On-site

$87K - $117K/yr

... engineering, operations and business development, to streamline contract workflows and mitigate ... Oversee maintenance and retrieval of contract documents/files and validated data, preparation of ...

... cleaning, validation, quality assurance, and preparation of analysis-ready datasets. * Develop ... Roles is contingent upon contract award. What You Will Need: * Must be a U.S. Citizen or Permanent ...

... cleaning, validation, and organization. * Implement industry-standard and custom metrics to ... Bachelor's degree in Engineering (Electrical, Mechanical, or similar) from an ABET-accredited ...

New

... cleaning, validation, and organization. * Implement industry-standard and custom metrics to ... Bachelor's degree in Engineering (Electrical, Mechanical, or similar) from an ABET-accredited ...

... RTES) contract in support of the Redstone Test Center mission to provide superior technical ... Develop and execute test plans for validating and debugging prototypes and production hardware.

Be Seen First

Meet the team: Our Engineers at the Airbus U.S. Manufacturing facility take our aircraft from ... Support is given on the process validation form (PVF) and failure analysis (FA). * Support on the ...

Manufacturing Engineer II (Contract)

Mobile, AL · On-site

$72K - $93K/yr

Our Engineers at the Airbus U.S. Manufacturing facility take our aircraft from concept to customer ... Support is given on the process validation form (PVF) and failure analysis (FA). * Support on the ...

Our Engineers at the Airbus U.S. Manufacturing facility take our aircraft from concept to customer ... Support is given on the process validation form (PVF) and failure analysis (FA). * Support on the ...

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Contract Cleaning Validation Engineer information

What is a contract cleaning validation engineer?

Contract Cleaning Validation Engineers are professionals who specialize in ensuring that cleaning procedures in manufacturing environments, especially in industries like pharmaceuticals and biotechnology, meet regulatory and quality standards. They are typically hired on a contract basis to validate and document that cleaning processes effectively remove contaminants and residues from equipment and facilities. Their work includes developing and executing cleaning validation protocols, analyzing test results, and preparing reports for regulatory compliance. These engineers play a crucial role in maintaining product safety and quality, and their expertise helps companies pass regulatory inspections. Contract Cleaning Validation Engineers often work with cross-functional teams and need strong knowledge of industry guidelines such as those from the FDA and EMA.

What are the key skills and qualifications needed to thrive as a contract cleaning validation engineer?

To thrive as a Contract Cleaning Validation Engineer, you need a strong background in chemical engineering, microbiology, or a related field, along with experience in cleaning validation within regulated industries. Familiarity with validation protocols, regulatory standards (such as FDA or EU GMP), and statistical analysis software is typically required. Attention to detail, problem-solving skills, and effective communication are crucial for documenting processes and collaborating with cross-functional teams. These skills ensure cleaning processes are compliant, reproducible, and safe, which is vital for product quality and regulatory approval.

What are some common challenges faced by a contract cleaning validation engineer during a project?

Contract Cleaning Validation Engineers often encounter challenges such as aligning cleaning protocols with both client requirements and regulatory standards, managing tight project timelines, and navigating complex equipment or facility layouts. Additionally, collaborating effectively with client teams and other contractors is crucial to ensure that validation documentation is accurate and comprehensive. Staying up-to-date with evolving industry regulations and best practices is also essential to delivering successful validation outcomes.

What is the difference between Contract Cleaning Validation Engineer vs Quality Assurance Specialist?

AspectContract Cleaning Validation EngineerQuality Assurance Specialist
CredentialsValidation certifications, engineering backgroundQA certifications, quality management training
Work EnvironmentPharmaceutical, biotech, or cleanroom facilitiesManufacturing, production, or laboratory settings
Employer & IndustryContract-based roles in regulated industriesIn-house or consulting roles in various industries
Search & Comparison IntentFocus on cleaning validation processesFocus on overall quality assurance practices

The Contract Cleaning Validation Engineer primarily specializes in validating cleaning processes within regulated environments like pharmaceuticals and biotech. In contrast, a Quality Assurance Specialist oversees broader quality systems, including audits and compliance. While both roles require understanding of industry standards, the validation engineer focuses on specific cleaning validation tasks, whereas the QA specialist manages overall quality assurance programs.

What are popular job titles related to Contract Cleaning Validation Engineer jobs in Alabama?

For Contract Cleaning Validation Engineer jobs in Alabama, the most frequently searched job titles are:

What job categories do people searching Contract Cleaning Validation Engineer jobs in Alabama look for?

The top searched job categories for Contract Cleaning Validation Engineer jobs in Alabama are:

What cities in Alabama are hiring for Contract Cleaning Validation Engineer jobs?

Cities in Alabama with the most Contract Cleaning Validation Engineer job openings:

Validation Engineer (Aseptic C&Q )

Centstone

Birmingham, AL • On-site

Contractor

Re-posted 22 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

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