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Contract Cleaning Validation Engineer Jobs (NOW HIRING)

Sebela Pharma

CQV/Validation Engineer

Holbrook, MA · On-site

$33 - $43/hr

Braintree Laboratories, Inc., a part of Sebela Pharmaceuticals, has its contract development and ... Support equipment, utility, facility, process, cleaning, and computerized system validation ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Perform risk assessments to support cleaning validation strategies ... Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams. * Analyze ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Perform risk assessments to support cleaning validation strategies ... Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams. * Analyze ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Perform risk assessments to support cleaning validation strategies ... Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams. * Analyze ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Perform risk assessments to support cleaning validation strategies ... Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams. * Analyze ...

Mativ

Validation Engineer

Dallas, TX · On-site

Validation Engineer Mativ is a global leader in specialty materials headquartered in Alpharetta ... Experience with validation of cleaning, software, automated systems, packaging and laboratory ...

New

Legalpmpartners

Cleaning Validation Specialist

Caguas, PR · On-site

$65 - $95/hr

Job Overview We are seeking an experienced Cleaning Validation Specialist to support regulated ... Collaborate with Quality, Manufacturing, Engineering, Validation, and Microbiology teams. * Analyze ...

GL Staffing Services, Inc.

Validation

Boca Raton, FL · On-site

$75K - $95K/yr

The Validation Specialist / Validation Engineer is responsible for planning, executing, documenting ... Clean Steam * Compressed Air * Nitrogen * Environmental Monitoring systems * Execute and/or support ...

New

INCOG

Senior Validation Engineer

Fishers, IN · On-site

The Senior Validation Engineer is responsible for understanding and implementing validation ... This includes, but is not limited to, clean utilities, autoclave, washer, filler, laboratory ...

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Contract Cleaning Validation Engineer information

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How much do contract cleaning validation engineer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for contract cleaning validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

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.

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Contract Cleaning Validation Engineer jobs near you
Infographic showing various Contract Cleaning Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 32% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Validation & Engineering Group Inc.

Holly Springs, NC • On-site

Full-time

Re-posted 9 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Engineer

Description:

The role demands deep technical expertise across the full validation lifecycle including URS development, FAT/SAT execution, and Computer System Validation (CSV) as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.

Key Responsibilities:

  • Develop User Requirement Specifications (URS).
  • Lead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.
  • Drive process design for new equipment and ensure product design requirements are met.
  • Execute commissioning and qualification activities for new and existing equipment.
  • Provide technical oversight to ensure equipment meets safety, regulatory, and operational standards.
  • Manage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.
  • Collaborate with Procurement and Legal on vendor contracts.
  • Create and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).
  • Optimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.
  • Lead design reviews, risk assessments, and FMEA to ensure reliability and performance.
  • Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.
  • Apply statistical analysis and SPC systems to support data-driven decision-making.
  • Manage multiple priorities and maintain equipment qualification schedules.

Qualifications:

  • Bachelor's degree in Engineering or Science.
  • Minimum 4 years of engineering experience in pharmaceutical and/or medical device industries.
  • Demonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).
  • Proven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.
  • Strong experience executing capital projects within GMP-regulated manufacturing environments.
  • Familiarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.
  • Ability to work independently and lead solutions under general direction.
  • Strong organization, and communication skills

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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