1

Ellab Jobs (NOW HIRING)

Must have experience with thermal validation using Ellab or equivalent systems, including thermocouple mapping and lethality validation. Must have experience leading or supporting sterilization ...

Must have experience with thermal validation using Ellab or equivalent systems, including thermocouple mapping and lethality validation. Must have experience leading or supporting sterilization ...

Experience with ELLAB data loggers and systems * Working knowledge of GMPs, OSHA compliance, 21 CFR Part 11 and cleanrooms, automated biopharmaceutical processing and plant equipment * Good ...

Ellab information

See salary details

$8

$26

$61

How much do ellab jobs pay per hour?

As of Jul 11, 2026, the average hourly pay for ellab in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Ellab Validation Engineer, and why are they important?

To thrive as an Ellab Validation Engineer, you need a solid background in engineering or life sciences, experience with validation protocols, and knowledge of regulatory standards such as GMP. Familiarity with Ellab thermal validation systems, data loggers, and related software is typically required. Attention to detail, problem-solving skills, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring precise documentation. These competencies are vital to guarantee compliance, data integrity, and successful validation of critical processes in regulated industries.

What is an Ellab and what do they do?

Ellab is not a job title, but rather the name of a company that specializes in providing validation and monitoring solutions for industries such as pharmaceuticals, food, and medical devices. Professionals who work at Ellab typically focus on thermal validation, calibration, and environmental monitoring to ensure product safety and regulatory compliance. Common roles at Ellab include engineers, technicians, and quality assurance specialists who use advanced equipment and software to collect and analyze critical process data.

What are the typical responsibilities of an Ellab validation engineer, and how does the role contribute to quality assurance in regulated industries?

As an Ellab validation engineer, your main responsibilities typically include planning, executing, and documenting thermal validation processes using Ellab equipment in industries such as pharmaceuticals, food, and healthcare. You will calibrate and maintain data loggers, run qualification protocols (IQ/OQ/PQ), and analyze results to ensure compliance with regulatory standards like FDA and GMP. Collaboration with quality assurance teams and production staff is common to resolve issues and optimize processes. Your work directly supports product safety and regulatory compliance, making it crucial to the organization's quality assurance efforts.

What is the difference between Ellab vs Validation Engineer?

AspectEllabValidation Engineer
Required CredentialsTypically technical certifications, industry-specific trainingEngineering degree, certifications like GxP or GMP often preferred
Work EnvironmentManufacturing, pharmaceutical, biotech labsPharmaceutical, biotech, medical device industries
Employer & Industry UsageManufacturers of validation and monitoring equipmentPharmaceutical companies, biotech firms, medical device manufacturers
Common Search & ComparisonEllab vs Validation Engineer

Ellab professionals focus on calibration, validation, and monitoring using specialized equipment, while Validation Engineers design and oversee validation processes. Both roles are essential in regulated industries like pharma and biotech, but Ellab roles are more equipment-focused, whereas Validation Engineers handle broader validation strategies.

More about Ellab jobs

Computer System Validation Engineer

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Posted 13 days ago


Job description

Job Title: Validation Engineer

Location: Indianapolis / Bloomington, IN (100% Onsite)

Duration: Long term Contract

Interview Mode: Onsite (Local candidates preferred)

Job Summary:

We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation activities, documentation migration, and equipment qualification to ensure compliance with regulatory standards.

Key Responsibilities

  • Lead migration of legacy validation documents into the Kneat digital platform, ensuring accuracy and compliance
  • Perform equipment qualification for lab instruments (pH meters, thermal mixers, peristaltic pumps, nutating mixers, etc.)
  • Execute temperature mapping studies, including work with Ellab systems or similar equipment
  • Support Computer Systems Validation (CSV) activities and documentation
  • Assist Process Engineering teams to ensure project timelines and milestones are met
  • Ensure all validation activities comply with GMP and regulatory requirements
  • Maintain clear, accurate, and compliant documentation

Required Qualifications:

  • Bachelor’s degree in Engineering, Science, or related field
  • 6+ years of experience in Computer Systems Validation (CSV)
  • 4+ years of experience in pharmaceutical manufacturing environment
  • Hands-on experience with equipment qualification and validation
  • Strong knowledge of CSV principles and regulatory compliance
  • Experience working in onsite, fast-paced environments