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Contract Cleaning Validation Engineer Jobs in Raleigh, NC

MedPharm

Sr. Process Engineer/Sr. Scientist

Durham, NC · On-site

$94K - $121K/yr

Job Summary The Sr. Process Engineer/Senior Scientist will lead late-stage development activities ... Support cleaning validation, equipment qualification, and continued process verification (CPV ...

MedPharm

Sr. Process Engineer/Sr. Scientist

Durham, NC · On-site

$94K - $121K/yr

Job Summary The Sr. Process Engineer/Senior Scientist will lead late-stage development activities ... Support cleaning validation, equipment qualification, and continued process verification (CPV ...

CRB

CQV Engineer III

Raleigh, NC

Lead or support execution of commissioning, qualification, and validation activities * Witness and ... clean utilities, HVAC, WFI, CIP/SIP, nitrogen, compressed air, etc.) * Working knowledge of cGMP ...

CRB

CQV Engineer III

Raleigh, NC · On-site

Lead or support execution of commissioning, qualification, and validation activities * Witness and ... clean utilities, HVAC, WFI, CIP/SIP, nitrogen, compressed air, etc.) * Working knowledge of cGMP ...

NCBiotech

QC Microbiology Lead (Raleigh, US)

Raleigh, NC · On-site

$110 - $150/hr

... validation, engineering, and packaging personnel in support of those functions. The qualified ... Environmental monitoring of clean rooms and facility water systems, kinetic LAL, gel-clot LAL ...

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All JobsContract Cleaning Validation Engineer JobsContract Cleaning Validation Engineer Jobs in Raleigh, NC

Contract Cleaning Validation Engineer information

See Raleigh, NC salary details

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

As of Aug 21, 2026, the average hourly pay for contract cleaning validation engineer in Raleigh, NC is $50.54, according to ZipRecruiter salary data. Most workers in this role earn between $38.32 and $61.44 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.

What are the most commonly searched types of Cleaning Validation Engineer jobs in Raleigh, NC?

The most popular types of Cleaning Validation Engineer jobs in Raleigh, NC are:

What are popular job titles related to Contract Cleaning Validation Engineer jobs in Raleigh, NC?

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

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The top searched job categories for Contract Cleaning Validation Engineer jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Contract Cleaning Validation Engineer jobs?

Cities near Raleigh, NC with the most Contract Cleaning Validation Engineer job openings:

Contract Cleaning Validation Engineer jobs near you

Sr. Process Engineer/Sr. Scientist

MedPharm

Durham, NC • On-site

$94K - $121K/yr

Full-time

Re-posted 5 days ago

Job description

Job Summary
The Sr. Process Engineer/Senior Scientist will lead late-stage development activities for topical and liquid oral pharmaceutical products, including process scale-up, technology transfer, commercial process validation, and manufacturing support. This role requires strong expertise in semisolid and liquid manufacturing processes, process robustness, troubleshooting, and regulatory compliance to support successful commercialization and lifecycle management.
Key Responsibilities
  • Lead late-stage formulation and process development activities for topical dosage forms (creams, ointments, gels, lotions) and liquid oral products (solutions, suspensions, syrups).
  • Design and execute scale-up, process optimization, and process characterization studies for commercial readiness.
  • Support technology transfer activities from R&D to pilot and commercial manufacturing sites, including CMOs/CDMOs.
  • Develop and review manufacturing process descriptions, batch manufacturing records (BMRs), process flow diagrams, and technical transfer documents.
  • Plan, execute, and document Process Performance Qualification (PPQ) and commercial process validation activities.
  • Provide technical oversight during exhibit, registration, validation, and commercial batches.
  • Troubleshooting issues related to mixing, homogenization, viscosity, phase separation, settling, aeration, filling, and hold time studies.
  • Technical support in investigations for deviations, OOS/OOT results, complaints, and CAPAs related to process or product performance.
  • Support cleaning validation, equipment qualification, and continued process verification (CPV) activities.
  • Collaborate closely with Analytical Development, Quality Assurance, Regulatory Affairs, Supply Chain, and Manufacturing teams.
  • Evaluate process data and statistical trends to ensure process consistency and robustness.
  • Support regulatory submissions, deficiency responses, audits, and inspections by providing technical documentation and SME support.
  • Ensure compliance with cGMP, FDA, EMA, ICH, and internal quality standards.

Required Qualifications
  • Master’s or Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related scientific discipline.
  • 6–10+ years of experience in pharmaceutical development and manufacturing, with significant exposure to topical and liquid oral dosage forms.
  • Strong hands-on experience with semisolid and liquid manufacturing equipment including:
    • Homogenizers
    • Vacuum manufacturing vessels
    • Agitators and mixers
    • Colloid mills
    • Liquid filling equipment
  • Experience in process scale-up, technology transfer, and commercial process validation.
  • Thorough understanding of rheology, emulsion systems, suspension stability, viscosity control, and preservative systems.
  • Strong knowledge of cGMP, DOE, QbD principles, process validation lifecycle, and regulatory expectations.
  • Experience authoring and reviewing validation protocols, technical reports, and manufacturing investigations.
  • Excellent technical writing, communication, and cross-functional collaboration skills.

Preferred Skills
  • Experience with SUPAC guidelines for semisolid and liquid products.
  • Knowledge of preservative efficacy studies, hold time studies, and in-use stability considerations.
  • Familiarity with process analytical tools and statistical analysis software.
  • Experience supporting FDA/EMA audits and commercial product lifecycle management.
  • Exposure to scale-up challenges associated with emulsion and suspension systems.

Technical Expertise Areas
  • Emulsion and suspension manufacturing
  • Viscosity and rheology optimization
  • Mixing and homogenization scale-up
  • Process validation (PPQ)
  • Technology transfer documentation
  • Cleaning validation support
  • Continued Process Verification (CPV)
  • Manufacturing investigations and CAPA
  • Commercial manufacturing support

Typical Deliverables
  • Technology transfer protocols and reports
  • PPQ/Process validation protocols and reports
  • Manufacturing risk assessments
  • Scale-up and process characterization reports
  • Batch troubleshooting investigations
  • CPV trend analysis reports
  • Regulatory submission support documents
  • Hold time and mixing studies documentation

 

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