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Lims Analyst Jobs in Raleigh, NC (NOW HIRING)

Preliminary Analysis : Calculate neutralization titers (like IC50/EC50) and total antibody ... LIMS experience is required. Experience with LabVantage is preferred. * Experience in a CLIA or ...

Quality Engineer

Durham, NC

$69K - $89K/yr

Strong analytical, organizational, and communication skills. Preferred * Experience supporting manufacturing start-up or scale-up environments. * Experience implementing or using MES, ERP, LIMS, or ...

Strong analytical, organizational, and communication skills. Preferred * Experience supporting manufacturing start-up or scale-up environments. * Experience implementing or using MES, ERP, LIMS, or ...

... analysis. Ability to work cross-functionally with middleware and LIMS teams to integrate the database. Applicable experience working on custom database development.

Quality Engineer

Benson, NC

$58K - $75K/yr

Strong analytical, organizational, and communication skills. Preferred * Experience supporting manufacturing start-up or scale-up environments. * Experience implementing or using MES, ERP, LIMS, or ...

Senior Analytical Chemist Location: Raleigh, NC Schedule: Fully Onsite | Monday-Friday | Normal ... Experience using Empower, CDS, LIMS, and other laboratory software systems. * Strong knowledge of ...

Showing results 41-60

Lims Analyst information

See Raleigh, NC salary details

$30.1K

$71.2K

$126.4K

How much do lims analyst jobs pay per year?

As of Sep 2, 2026, the average yearly pay for lims analyst in Raleigh, NC is $71,212.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,000.00 and $84,600.00 per year, depending on experience, location, and employer.

What is a LIMS analyst?

A LIMS Analyst is responsible for managing and maintaining a Laboratory Information Management System (LIMS), which is used to track samples, manage data, and ensure compliance with regulatory standards. They configure the system to meet laboratory needs, troubleshoot issues, and provide user support. Additionally, they may assist with system validation, data integrity, and process automation to improve laboratory efficiency.

What are the typical daily responsibilities of a LIMS analyst?

As a Lims Analyst, your daily responsibilities usually involve configuring and maintaining the Laboratory Information Management System, troubleshooting user issues, and ensuring data integrity across laboratory processes. You may also work closely with scientists, IT personnel, and quality assurance teams to streamline workflows, implement system updates, and provide training or support to end users. This role often requires balancing technical problem-solving with clear communication to facilitate efficient lab operations. The variety of tasks provides valuable experience and can open up further career advancement opportunities in IT, laboratory management, or quality systems.

What are the key skills and qualifications needed to thrive in the LIMS analyst position, and why are they important?

To thrive as a Lims Analyst, you need a solid background in laboratory operations, data management, and quality assurance, typically supported by a degree in a scientific field or information technology. Experience with Laboratory Information Management Systems (LIMS), data analysis tools, and relevant certifications such as CLIA or ISO standards are highly valued. Strong problem-solving abilities, attention to detail, and effective communication skills help distinguish top performers in this position. These skills are vital for ensuring accurate data tracking, regulatory compliance, and smooth laboratory workflow integration.

What cities near Raleigh, NC are hiring for Lims Analyst jobs?

Cities near Raleigh, NC with the most Lims Analyst job openings:

Infographic showing various Lims Analyst job openings in Raleigh, NC as of August 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 100% In-person job distribution, with an average salary of $71,212 per year, or $34.2 per hour.

Senior QC Analyst (2nd Shift) - In-Process

KBI Biopharma, Inc.

Durham, NC • On-site

$63K - $86K/yr

Full-time

Re-posted 2 days ago


KBI Biopharma rating

6.5

Company rating: 6.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz


Job description

This role contains the following responsibilities covering 2nd shift hours (2:00 pm through 10:30 pm), Monday through Friday:

Position Summary:

The Senior QC Analyst (2nd Shift) will be trained to execute analytical test methods and their corresponding analytical techniques. The core function is composed of completing QC testing for in-process, characterization, release, or stability samples. Additionally, when need arises, Senior QC Analyst will assist with troubleshooting and support In-process Support Associates with STAT samples during 2nd shift.

Responsibilities include:

  • In-process, characterization, stability, and/or release testing as assigned. Capabilities include (but not limited to) HPLC, ELISA, qPCR, SoloVPE, other spectrophotometric techniques, capillary electrophoretic techniques, and compendial testing per USP with near-zero error and minimal guidance or direction
  • Execution of method transfer, method qualification, and/or method validation testing performed under protocol
  • Solution preparation
  • Organizes and processes samples according to GxP standards
  • Independent analysis and collation of data to draw conclusions
  • Enter data into control charts and LIMS, if applicable
  • Supports lab investigation and deviation reports
  • Supports implementation of Corrective and Preventive Actions
  • Revises SOPs and technical documents
  • Supports team to troubleshoot testing or project challenges with comfort in presenting and communicating data
  • Tracks department metrics upon request; actively engages in improvement of department metrics
  • Partakes in continuous improvement projects or leading simple improvement projects
  • Ensures state of safety and regulatory audit readiness at all times
  • Maintains work to current Good Manufacturing Practices (cGMP)
  • Ensures Trainer qualification status to expand team matrix
  • Laboratory support - ensures areas are neat, clean, organized, and equipment is functioning
  • Participates in data review activities
  • Duties may include support in STAT testing coordination
  • It is the expectation that this position is required to be onsite full time with a minimum of 75% of time in the laboratory/facility

Minimum Requirements:

Relevant degree and 4-8 years' biopharmaceutical industry experience, preferably in protein analytics

Salary: $63,000-$86,900

KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.


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