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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

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

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

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

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 (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

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 ...

Columbus McKinnon Corporation

2nd Shift Janitor

Damascus, VA · On-site

$12 - $15.25/hr

Work with a contract cleaning service when necessary. Knowledge, Skills, Competencies, and ... engineering know-how. Columbus McKinnon is a publicly traded company that has been in business for ...

TekSynap

Cybersecurity Engineer

Fort Belvoir, VA · On-site

... validating complex technical solutions, and connecting business, system, and data flows. Overview We are seeking a DTRA CSSP Cybersecurity Engineer to join our Prime Contract with the Defense Threat ...

TekSynap

Cybersecurity Engineer

Fort Belvoir, VA · On-site

Overview We are seeking a DTRA CSSP Cybersecurity Engineer to join our Prime Contract with the ... Ensure all inbound subscriber log feeds are continuously validated, parsed, and normalized against ...

TekSynap

Cybersecurity Engineer

Fort Belvoir, VA · On-site

... validating complex technical solutions, and connecting business, system, and data flows. Overview We are seeking a DTRA CSSP Cybersecurity Engineer to join our Prime Contract with the Defense Threat ...

TekSynap

Cybersecurity Engineer

Fort Belvoir, VA · On-site

... validating complex technical solutions, and connecting business, system, and data flows. Overview We are seeking a DTRA CSSP Cybersecurity Engineer to join our Prime Contract with the Defense Threat ...

TekSynap

Cybersecurity Engineer

Fort Belvoir, VA · On-site

Overview We are seeking a DTRA CSSP Cybersecurity Engineer to join our Prime Contract with the ... Ensure all inbound subscriber log feeds are continuously validated, parsed, and normalized against ...

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All JobsContract Cleaning Validation Engineer JobsContract Cleaning Validation Engineer Jobs in Virginia

Contract Cleaning Validation Engineer information

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 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 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 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.

TSMS- Sr. Scientist

Eli Lilly and Company

Richmond, VA • On-site

$90K - $123K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Senior Scientist - Technical Services/Manufacturing Sciences (TS/MS) Cleaning
As our biologics pipeline continues to expand, Eli Lilly & Company has invested in a state-of-the-art new facility in Richmond, VA. To support this exciting new GMP manufacturing facility and ensure a safe and successful start-up, we are seeking talented individuals to contribute to establishing Lilly Richmond as a reliable supplier of our innovative medicines and furthering our goal of making a difference to people's lives.
The TS/MS Sr. Scientist is responsible for supporting the cleaning program for process equipment and ancillary components in the manufacturing facility. The role will provide technical support for introducing and supporting biologics manufacturing processes from startup through routine operations.
Key Responsibilities
  • 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
  • Generate cleaning validation protocols and summary reports
  • Execute cleaning validation protocols, including visual inspection and sampling and coordination with other support groups (e.g. operations, maintenance, lab, etc.)
  • Author cleaning procedures and associated work instructions for all equipment
  • Develop cleaning batch records or appropriate documents to enable execution of cleaning activities on the production floor
  • Complete review of executed cleaning batch records/documentation
  • Trouble-shoot issues with and optimize cleaning cycles and/or cleaning equipment
  • Provides technical support on cleaning deviations/events and assist in root cause analysis.
  • Completes changes associated with cleaning equipment, cleaning cycles and cleaning program.
  • Completes Periodic Review Reports for key components to ensure cleaning
  • equipment remains in a qualified state

Basic Requirements:
  • BS in Biochemistry, Biotechnology, Chemical Engineering or related discipline
  • A minimum of 3 years of experience within the biopharmaceutical or GMP industry
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Additional Preferences:
  • MS in Biochemistry, Biotechnology, Chemical Engineering or related discipline
  • Technical knowledge of cleaning equipment (CIP skids, Parts washers, etc.) and cleaning regimes (chemical, re-circulated washing, etc.)
  • Knowledge of qualification/validation requirements and good documentation practices
  • Knowledge of biologics manufacturing processes and understanding of production schedules
  • Strong written and verbal communication skills
  • Ability to work on own initiative and as part process team consisting of a diverse group of management, production/science and engineering professionals.
  • Demonstrated technical capability with high productivity.
  • Self-starter with high initiative and data-driven approach to problem-solving.
  • Demonstrated strong interpersonal skills.
  • Demonstrated adaptability and flexibility to working in different environments and teams.

Work Environment:
  • Onsite
  • This is an 8-hour day role. As a manufacturing support function, the need for occasional evening or weekend support can arise.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$79,500 - $171,600
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly

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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876

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