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Ellab Jobs (NOW HIRING)

Moderna, Inc.

CQV Engineer II

Norwood, MA · On-site

$74K - $118.40K/yr

Utilize validation tools and qualification equipment (including data loggers such as Ellab) to support qualification activities. * Contribute to maintaining facilities and equipment in a continuous ...

Moderna Therapeutics

CQV Engineer II

Norwood, MA · Hybrid

$74K - $118.40K/yr

Utilize validation tools and qualification equipment (including data loggers such as Ellab) to support qualification activities. * Contribute to maintaining facilities and equipment in a continuous ...

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How much do ellab jobs pay per hour?

As of May 31, 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 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 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 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
What job categories do people searching Ellab jobs look for? The top searched job categories for Ellab jobs are:
Ellab jobs near you
Infographic showing various Ellab job openings in the United States as of May 2026, with employment types broken down into 82% Full Time, and 18% Contract. Highlights an 91% Physical, and 9% Hybrid job distribution, with an average salary of $54,791 per year, or $26.3 per hour.
6365 - Senior CQV Engineer / Senior Validation Engineer

6365 - Senior CQV Engineer / Senior Validation Engineer

Verista, Inc.

Devens, MA • On-site

$70.49K - $118.06K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago

Job description

Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Senior Validation Engineer Responsibilities:
  • Execute IQ/OQ protocols and support operational verification activities
  • Perform Drawing walkdowns (P&IDs, system verification)
  • Perform Equipment/component verification
  • Perform MOC and weld verification
  • Support temperature mapping activities using data loggers and validation tools
  • Assist with SIP/CIP execution and cycle development activities
  • Identify and document deviations and support investigations
  • Ensure accurate and complete documentation in compliance with GMP/GDP standards
  • Work collaboratively with engineering, QA, and operations teams

Job Requirements:
  • Bachelor's Degree or equivalent required (STEM degree, Biomedical Engineering, Chemical Engineering preferred)
  • 3-8 years of CQV/validation experience
  • Hands-on experience executing validation for process equipment
  • Strong GMP/GDP fundamentals
  • Experience with IQ/OQ execution and field verification activities
  • Experience with eVal (required), ValGenesis a plus
  • Exposure to temperature mapping (Ellab a plus)
  • Experience with bioprocess equipment preferred (bioreactors, filtration, chromatography, UF)

This role requires the ability to be on-site, full-time in Devens, MA.
For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
*Verista is an equal opportunity employer.
National (US) Range
$70,491-$118,062 USD
Benefits
Why Choose Verista?
  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com

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