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Lims Professional Jobs (NOW HIRING)

Onterris

Senior Software Engineer - LIMS Modernization

$200K - $210K/yr

Our scientists, engineers, field teams,consultantsand professionals collaborate across disciplines ... A Day in the Life CT LIMS is our most significant piece of custom-built enterprise software: a ...

Saviance

Senior Java/AWS Engineer -with LIMS

Boston, MA · On-site

$135K - $178K/yr

They are seeking a skilled Senior Java/AWS Engineer -with LIMS to collaboratively solve complex ... Saviance is a modern consulting firm providing a variety of professional services to its clients in ...

Clinisys

Professional Services Consultant

Tucson, AZ · On-site +1

Provide ongoing support and training to laboratory staff and stakeholders on LIMS usage and best ... Professional Services Locations USA Remote Remote status Fully Remote Employment type Full-time

CareDx, Inc.

Staff Software Engineer

Brisbane, CA · On-site

... years of professional software engineering experience, with significant hands-on work in LIMS environments. • Extensive experience configuring and customizing LIMS platforms such as Labbit ...

CareDx, Inc.

Staff Software Engineer

Brisbane, CA · On-site

Experience: 8 to 10+ years of professional software engineering experience, with significant hands-on work in LIMS environments. * Extensive experience configuring and customizing LIMS platforms such ...

CareDx, Inc.

Staff Software Engineer

Brisbane, CA · On-site

Experience: 8 to 10+ years of professional software engineering experience, with significant hands-on work in LIMS environments. * Extensive experience configuring and customizing LIMS platforms such ...

KēSTA I.T.

Business Analyst

Salt Lake City, UT · Hybrid

$53.56 - $83.56/hr

... professional experience. Preferred Qualifications · Hands-on experience with LabWare LIMS v8 administration and development. · Laboratory Informatics experience. · Experience supporting public ...

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Lims Professional information

What is the difference between Lims Professional vs Laboratory Technician?

AspectLims ProfessionalLaboratory Technician
CredentialsTypically requires a degree in life sciences or related field, with certifications in laboratory information management systems (LIMS)Usually requires a high school diploma or associate degree, with some technical training
Work EnvironmentWorks primarily with LIMS software, data management, and quality control in labsPerforms sample testing, data recording, and basic lab procedures
Industry UsageCommon in biotech, pharmaceutical, and clinical labs for data managementFound in similar settings, focusing on sample processing and testing

The main difference is that Lims Professionals focus on managing laboratory data and systems, requiring specialized software knowledge, while Laboratory Technicians perform hands-on testing and sample analysis. Both roles are essential in laboratory operations but differ in responsibilities and skill requirements.

What is a LIMS professional job description?

A LIMS (Laboratory Information Management System) professional is responsible for implementing, maintaining, and optimizing laboratory software systems that manage data, samples, and workflows. They often collaborate with lab staff to ensure system accuracy, troubleshoot issues, and may require knowledge of database management, programming, and industry regulations. Certification and technical skills are typically important for this role.

What cities are hiring for Lims Professional jobs?

Cities with the most Lims Professional job openings:

What are the most commonly searched types of Lims jobs?

The most popular types of Lims jobs are:

What states have the most Lims Professional jobs?

States with the most job openings for Lims Professional jobs include:

What job categories do people searching Lims Professional jobs look for?

The top searched job categories for Lims Professional jobs are:

Lims Professional jobs near you
Infographic showing various Lims Professional job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 21% Part Time, and 5% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution.

Quality Data Steward (LIMS/eQMS) - Pharma Mfg

Kelly Services

Raleigh, NC

$76K - $110K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 15 days ago

Job description

Quality Data Steward (LIMS/eQMS) – Pharmaceutical Manufacturing
Location: Raleigh, NC
Schedule: Fully Onsite | Monday–Friday | Normal Business Hours
Salary: $76,000–$110,000
Position Summary
The Data Steward is responsible for ensuring the accuracy, integrity, security, and compliance of quality-related electronic data across regulated systems including LIMS, SAP, and eQMS. This role supports data governance by maintaining data standards, monitoring data quality, and ensuring compliance with FDA, cGMP, 21 CFR Part 11, EU GMP Annex 11, and ALCOA+ principles. Working cross-functionally with Quality, Manufacturing, IT, Regulatory Affairs, and Supply Chain, the Data Steward helps drive data integrity, regulatory compliance, and informed business decisions.
Key Responsibilities
  • Administer and maintain LIMS to ensure data accuracy, integrity, security, and regulatory compliance.
  • Serve as the subject matter expert (SME) for LIMS by providing system support, troubleshooting, and issue resolution.
  • Support SAP Quality Management functions, including master data, system enhancements, upgrades, and troubleshooting.
  • Monitor data quality, investigate data anomalies, and implement corrective actions.
  • Support implementation, validation, and maintenance of electronic quality systems and system upgrades.
  • Author, review, and maintain SOPs, specifications, protocols, reports, and system documentation.
  • Ensure compliance with cGMP, FDA regulations, 21 CFR Part 11, EU GMP Annex 11, ALCOA+, and internal quality systems.
  • Support Computer System Validation (CSV) activities, including change controls, risk assessments, testing, and validation documentation.
  • Assist with internal audits, regulatory inspections, data integrity assessments, CAPAs, and remediation activities.
  • Generate, analyze, and report laboratory and quality data to identify trends and support investigations.
  • Support Annual Product Reviews (APRs), quality metrics, and management reporting.
  • Train users on LIMS, SAP, electronic systems, and data management processes.
  • Collaborate with Quality, Manufacturing, IT, Regulatory Affairs, and Supply Chain to resolve system and data-related issues.
  • Perform additional duties and special projects as assigned.
Qualifications
Required
  • Bachelor's degree in a scientific, technical, or related field.
  • Minimum of five (5) years of experience in the pharmaceutical, biotechnology, medical device, or other regulated industry.
  • Experience with LIMS, SAP Quality Management, eQMS, or other electronic quality systems.
  • Strong knowledge of cGMP, FDA regulations, 21 CFR Part 11, EU GMP Annex 11, and ALCOA+ data integrity principles.
  • Experience supporting data governance, electronic data management, and quality systems.
  • Strong analytical, troubleshooting, organizational, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Proficiency with Microsoft Office applications, including Excel, Word, and PowerPoint.
Preferred
  • Experience with Computer System Validation (CSV) and change control.
  • Experience supporting audits, regulatory inspections, CAPAs, investigations, and quality risk assessments.
  • Familiarity with laboratory operations, analytical testing, and Quality Control environments.
  • Experience with quality metrics, data analysis, and reporting.
  • Lean Six Sigma, ASQ, or other quality certifications are a plus.
Work Environment
  • Fully onsite position based in Raleigh, NC.
  • Standard Monday–Friday business hours.
  • Office-based role with regular interaction in laboratory and manufacturing environments.
  • Frequent computer-based work involving electronic quality systems and data management.
  • Must be able to wear appropriate PPE when entering laboratory or manufacturing areas.
  • Occasional schedule flexibility may be required to support audits, system implementations, validation activities, or business needs.

 
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.