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Contract Cleaning Validation Engineer Jobs in Virginia

Eli Lilly and Company

TSMS- Sr. Scientist

Richmond, VA · On-site

$90K - $123K/yr

Develop cleaning strategy in collaboration with Engineering and Quality counterparts for Lilly Limerick Monoclonal Facility * Author and owns the Cleaning Validation Master Plan for the facility

Initial Therapeutics, Inc.

TSMS- Sr. Scientist

Richmond, VA · On-site

$79.50 - $171.60/hr

Develop cleaning strategy in collaboration with Engineering and Quality counterparts for the Lilly Limerick Monoclonal Facility. * Author and own the Cleaning Validation Master Plan for the facility.

New

Eli Lilly and Company

TSMS- Sr. Scientist

Richmond, VA

$90K - $123K/yr

Develop cleaning strategy in collaboration with Engineering and Quality counterparts for Lilly Limerick Monoclonal Facility * Author and owns the Cleaning Validation Master Plan for the facility

Cymertek Corporation

Test Engineer

Reston, VA · On-site

$90 - $125/hr

... validate the functionality, performance, and security of our applications. You will work closely ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

New

Cymertek Corporation

Test Engineer

Chantilly, VA · On-site

$85 - $125/hr

... validate the functionality, performance, and security of our applications. You will work closely ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

New

Cymertek

Test Engineer

Chantilly, VA · On-site

... validate the functionality, performance, and security of our applications. You will work closely ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

Cymertek

Test Engineer

Reston, VA · On-site

... validate the functionality, performance, and security of our applications. You will work closely ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

Cymertek

Test Engineer

Tysons, VA · On-site

... validate the functionality, performance, and security of our applications. You will work closely ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

Cymertek Corporation

QA Engineer

Reston, VA · On-site

$75 - $110/hr

... Validation Engineer, Manual Tester, QA Analyst, Software Quality Engineer, Test Automation ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

New

Cymertek

Test Engineer (Automated Testing)

Tysons, VA · On-site

... Validation Engineer, Software Quality Engineer, Test Lead, etc. DEGREE (Level Desired) Bachelor ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

Cymertek

Test Engineer (Automated Testing)

Reston, VA · On-site

... Validation Engineer, Software Quality Engineer, Test Lead, etc. DEGREE (Level Desired) Bachelor ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

Cymertek

QA Engineer

Reston, VA · On-site

... Validation Engineer, Manual Tester, QA Analyst, Software Quality Engineer, Test Automation ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

Cymertek Corporation

QA Engineer

Chantilly, VA · On-site

$90 - $120/hr

... Validation Engineer, Manual Tester, QA Analyst, Software Quality Engineer, Test Automation ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

Cymertek

QA Engineer

Tysons, VA · On-site

... Validation Engineer, Manual Tester, QA Analyst, Software Quality Engineer, Test Automation ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

Cymertek

QA Engineer

Chantilly, VA · On-site

... Validation Engineer, Manual Tester, QA Analyst, Software Quality Engineer, Test Automation ... Most contracts allow additional experience (4-5 years) in lieu of a Bachelor's Degree. Some ...

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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 the most commonly searched types of Cleaning Validation Engineer jobs in Virginia?

The most popular types of Cleaning Validation Engineer jobs in Virginia are:

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

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

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

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

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

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

Contract Cleaning Validation Engineer jobs near you
Infographic showing various Contract Cleaning Validation Engineer job openings in Virginia as of August 2026, with employment types broken down into 33% Full Time, 33% Part Time, and 34% Contract. Highlights an 100% In-person job distribution.

Engineer II, Validation

Thermo Fisher Scientific

Middletown, VA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 25 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 428 frontline employees who took The Breakroom Quiz

175th of 543 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Warehouse, Will work with hazardous/toxic materials
Job Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every day by enabling our customers to make the world healthier, cleaner and safer. We provide our global teams with resources to support individual career goals while advancing science and developing solutions for some of the world's toughest challenges.
Position Summary
Thermo Fisher Scientific's Clinical Diagnostic Reagents (CDR) group is seeking a Validation Engineer to support the planning, execution, and documentation of validation activities for clinical diagnostic reagent manufacturing within a cGMP, FDA-regulated, and ISO 13485 environment.
This role supports the qualification and validation lifecycle for manufacturing equipment, processes, facilities, utilities, and applicable systems. The Validation Engineer will develop and execute validation protocols, analyze results, prepare validation documentation, and support periodic reviews and gap assessments to maintain validated states and continued compliance with site and regulatory requirements.
The position works cross-functionally with Engineering, Quality, Manufacturing, and other site partners and receives guidance from senior validation engineering resources.
Location: Middletown, Virginia (fully onsite)
Relocation: Relocation assistance is not provided.
Key Responsibilities
  • Support the development, implementation, and maintenance of Validation Master Plans (VMPs) for facility equipment, systems, utilities, and manufacturing processes.
  • Author, revise, review, and execute validation and qualification protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documentation.
  • Analyze validation data and document results to verify that equipment, systems, and processes meet predefined requirements and acceptance criteria.
  • Prepare validation reports and supporting documentation in accordance with applicable site procedures and quality-system requirements.
  • Participate in periodic validation reviews, gap assessments, and lifecycle evaluations to help ensure systems and processes remain in a validated state.
  • Identify validation gaps and collaborate with appropriate stakeholders to develop and implement remediation plans.
  • Apply risk-based approaches to validation planning, execution, and documentation.
  • Collaborate with Engineering, Quality, Manufacturing, and other cross-functional partners to plan and coordinate validation activities.
  • Support validation deviations, investigations, root cause analyses, CAPAs, and associated corrective and preventive actions.
  • Support change-control activities involving validated equipment, processes, utilities, and systems, including assessment of potential validation impact.
  • Maintain accurate and complete validation records in accordance with site quality systems and applicable data-integrity requirements.
  • Support calibration coordination, verification activities, and documentation associated with equipment used in validated processes.
  • Support validation activities associated with applicable automation and computerized systems.
  • Contribute to continuous improvement of site validation practices, templates, procedures, and documentation.
  • Support internal and external audits and regulatory inspections, as needed.
  • Manage assigned validation activities and priorities to meet established project and production timelines.
Minimum Qualifications
  • Bachelor's degree in Engineering, Life Sciences, Chemistry, or a related scientific or technical discipline.
  • 2+ years of relevant validation, qualification, engineering, or quality experience in a regulated or similarly controlled environment.
  • Experience authoring, reviewing, and/or executing validation or qualification documentation, including IQ, OQ, and/or PQ protocols.
  • Strong technical writing and documentation skills.
  • Strong analytical, data-review, and problem-solving capabilities.
  • Ability to interpret technical requirements, evaluate results against predefined acceptance criteria, and document conclusions clearly.
  • Ability to manage multiple assignments and priorities within established timelines.
  • Ability to collaborate effectively with cross-functional teams.
  • Proficiency with Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint.
  • Ability to work onsite and enter manufacturing and cleanroom environments as required.
Knowledge and Skills
  • Understanding of validation and qualification lifecycle principles.
  • Familiarity with cGMP and regulated quality-system requirements.
  • Familiarity with risk-based quality and problem-solving methodologies such as FMEA, risk analysis, root cause analysis, and CAPA.
  • Understanding of change control and its relationship to maintaining validated systems and processes.
  • Strong attention to detail and commitment to accurate, traceable, and complete documentation.
  • Effective written and verbal communication skills.
  • Ability to work both independently on assigned activities and collaboratively within cross-functional teams.
Preferred Qualifications
  • Validation or qualification experience within medical device, diagnostics, pharmaceutical, biotechnology, or other regulated manufacturing environments.
  • Working knowledge of applicable FDA regulations, ISO 13485, GAMP 5, and cGMP requirements.
  • Experience developing and executing IQ/OQ/PQ protocols for manufacturing equipment, processes, facilities, utilities, or related systems.
  • Experience with risk-based validation methodologies and validation lifecycle management.
  • Experience supporting periodic reviews, validation gap assessments, and remediation activities.
  • Experience supporting deviations, investigations, root cause analysis, CAPA, and change control.
  • Familiarity with calibration and metrology principles.
  • Experience with manufacturing automation and/or computerized system validation (CSV).
  • Familiarity with electronic quality management systems or validation/document-management systems.
  • Knowledge of statistical analysis, process capability, or statistical process control methods.
  • Experience supporting audits or regulatory inspections in a regulated manufacturing environment.
Core Competencies
  • Analytical thinking and structured problem solving.
  • Clear and concise technical communication.
  • Strong organization and attention to detail.
  • Effective cross-functional collaboration.
  • Ability to balance multiple priorities and meet established deadlines.
  • Commitment to quality, compliance, and continuous improvement.

Compensation and Benefits
The salary range estimated for this position based in Virginia is $60,000.00-$90,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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