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Cleaning Validation Jobs in Raleigh, NC (NOW HIRING)

MedPharm

Sr. Process Engineer/Sr. Scientist

Durham, NC · On-site

$94K - $121K/yr

Support cleaning validation, equipment qualification, and continued process verification (CPV) activities. * Collaborate closely with Analytical Development, Quality Assurance, Regulatory Affairs ...

MedPharm

Sr. Process Engineer/Sr. Scientist

Durham, NC · On-site

$94K - $121K/yr

Support cleaning validation, equipment qualification, and continued process verification (CPV) activities. * Collaborate closely with Analytical Development, Quality Assurance, Regulatory Affairs ...

Syner-G

Sr. Validation Engineer

Raleigh, NC · On-site

Lead the generation and execution of validation lifecycle documentation (FAT, SAT, IOQ, PQ) for equipment, utilities, facilities, cleaning processes, shipping systems, and other GMP‑regulated ...

Syner-G

Sr. Validation Engineer

Raleigh, NC

Lead the generation and execution of validation lifecycle documentation (FAT, SAT, IOQ, PQ) for equipment, utilities, facilities, cleaning processes, shipping systems, and other GMPregulated assets.

Syner-G

Sr. Validation Engineer

Raleigh, NC · On-site

Lead the generation and execution of validation lifecycle documentation (FAT, SAT, IOQ, PQ) for equipment, utilities, facilities, cleaning processes, shipping systems, and other GMP-regulated assets.

Valspec

Process Validation Engineer

Raleigh, NC · On-site

$70 - $80/hr

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... Process Engineer -- Upstream / Downstream / Clean Utilities (Consultant) -- Contract Engagement:

Fujifilm

QA Specialist, Validation

Holly Springs, NC · On-site

Manufacturing (Clean Room) shop floor support for issue resolution, as needed. * Participates in ... Experience in Validation and/or Quality oversight, in an FDA regulated facility. Preferred ...

New

Fujifilm

QA Specialist, Validation

Holly Springs, NC · On-site

Manufacturing (Clean Room) shop floor support for issue resolution, as needed. * Participates in ... Experience in Validation and/or Quality oversight, in an FDA regulated facility. Preferred ...

New

Fujifilm

QA Specialist, Validation

Holly Springs, NC · On-site

Manufacturing (Clean Room) shop floor support for issue resolution, as needed. * Participates in ... Experience in Validation and/or Quality oversight, in an FDA regulated facility. Preferred ...

Home Clean Heroes

House Cleaning Specialist

Raleigh, NC · On-site

$14 - $20/hr

Home Clean Heroes is not your regular maid service - we are a fresh take on the home cleaning ... A good driver with a valid license without restrictions required * Comfortable working in homes ...

Solomon Page

Quality Assurance Engineer

Oxford, NC · On-site

$46/hr

Author and execute validation protocols (cleaning, process, systems), assess the impact of changes and deviations on validated states, and ensure all processes meet regulatory requirements. * Lead ...

Block by Block

Cleaning Associate

Durham, NC · On-site

$21.90/hr

Cleaning Ambassador Pay Range: $21.90 to $21.90 per hour (Weekly Pay & Pay Advance Before Pay Day!) Valid Driver's License PREFERRED Shift Details: Friday-Saturday 3pm-11pm Sunday-Tuesday 2pm-10:30pm ...

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Showing results 21-40

All JobsCleaning Validation JobsCleaning Validation Jobs in Raleigh, NC

Cleaning Validation information

See Raleigh, NC salary details

$35

$38

$41

How much do cleaning validation jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for cleaning validation in Raleigh, NC is $38.32, according to ZipRecruiter salary data. Most workers in this role earn between $36.92 and $39.71 per hour, depending on experience, location, and employer.

What is the job description of cleaning validation?

Cleaning validation is a process used in pharmaceutical and manufacturing industries to ensure that cleaning procedures effectively remove contaminants from equipment and surfaces. The job involves developing, executing, and documenting validation protocols, performing residue testing, and ensuring compliance with regulatory standards. Skills in analytical testing, attention to detail, and knowledge of Good Manufacturing Practices (GMP) are essential for this role.

What is the difference between Cleaning Validation vs Microbiologist?

AspectCleaning ValidationMicrobiologist
Required credentialsGMP, GMP-related certifications, technical trainingBiology, microbiology degrees, certifications
Work environmentPharmaceutical, biotech manufacturing facilitiesLaboratories, research facilities, healthcare settings
Employer and industry usagePharmaceutical, biotech, food industriesHealthcare, research, environmental testing

Cleaning Validation focuses on ensuring that cleaning processes effectively remove contaminants from equipment, primarily in manufacturing settings. Microbiologists study microorganisms, their behaviors, and control methods, often working in labs. While both roles require scientific knowledge and certifications, Cleaning Validation specialists concentrate on process validation in production environments, whereas Microbiologists focus on microbial analysis and research.

How do you become a cleaning validation consultant?

To become a cleaning validation consultant, professionals typically need a background in pharmaceutical or biotech manufacturing, quality assurance, or related fields, along with knowledge of validation processes and regulatory requirements such as FDA or EMA guidelines. Gaining experience through roles in validation, quality control, or manufacturing, and obtaining certifications like ASQ Certified Quality Auditor or specific validation training, can enhance credibility. Strong analytical skills, attention to detail, and familiarity with cleaning procedures and documentation are essential for success in this role.

What does cleaning validation do?

Cleaning validation is a process used in quality assurance roles to ensure that cleaning procedures effectively remove contaminants from equipment, preventing cross-contamination and ensuring product safety. It involves testing and documenting cleaning processes, often requiring knowledge of regulatory standards and analytical methods. Proper cleaning validation helps maintain compliance and product quality in regulated industries.
What job categories do people searching Cleaning Validation jobs in Raleigh, NC look for? The top searched job categories for Cleaning Validation jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Cleaning Validation jobs? Cities near Raleigh, NC with the most Cleaning Validation job openings:
Cleaning Validation jobs near you
Infographic showing various Cleaning Validation job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 29% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 100% Physical job distribution, with an average salary of $79,710 per year, or $38.3 per hour.

Sr. Process Engineer/Sr. Scientist

MedPharm

Durham, NC • On-site

$94K - $121K/yr

Full-time

Posted 26 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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