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Lims Manager Jobs in Florida (NOW HIRING)

Proficiency in Microsoft Excel, statistical tools, and Laboratory Information Management Systems (LIMS). * Strong knowledge of cGMP, GDP, and data integrity principles. * Excellent attention to ...

Ability to manage multiple priorities in a fast-paced operational environment. * Experience with LIS, LIMS, laboratory middleware, instrument interfaces, or clinical laboratory workflows. * Knowledge ...

Quality Control Analyst I

Sunrise, FL · On-site

$23 - $30.75/hr

Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS ...

Quality Control Coordinator

Miami, FL · On-site

$19 - $26/hr

Additional responsibilities may involve stability support/sample logistics and LIMS. * Communicates progress to management * Additional responsibilities may include the following in order to support ...

Quality Control Coordinator

Miami, FL · On-site

$19 - $26/hr

Additional responsibilities may involve stability support/sample logistics and LIMS. * Communicates progress to management * Additional responsibilities may include the following in order to support ...

... management, staff, clients, and regulatory agencies Independent critical thinking and creative problem-solving skills Proficient in Microsoft Excel, and Word, and LIMS

Minimum 5 years of experience working with AES LIMS application and database components ... Ability to communicate effectively with management. * Candidate must follow client standards and ...

Showing results 41-60

Lims Manager information

See Florida salary details

$17.2K

$45.8K

$76.6K

How much do lims manager jobs pay per year?

As of Aug 10, 2026, the average yearly pay for lims manager in Florida is $45,847.00, according to ZipRecruiter salary data. Most workers in this role earn between $32,900.00 and $51,600.00 per year, depending on experience, location, and employer.

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

To thrive as a Lims Manager, a strong background in laboratory science, data management, and experience with Laboratory Information Management Systems (LIMS) is essential, often supported by a relevant bachelor’s degree. Familiarity with LIMS software such as LabWare, STARLIMS, or Thermo Fisher, as well as certifications in data integrity or system administration, are highly valued. Excellent problem-solving, communication, and leadership skills help manage teams and facilitate collaboration across laboratory and IT departments. These competencies are crucial for ensuring accurate information flow, regulatory compliance, and efficient laboratory operations.

What is a lims manager?

A LIMS (Laboratory Information Management System) Manager is responsible for overseeing the implementation, maintenance, and optimization of a laboratory's data management system. They ensure that the LIMS software supports lab workflows, regulatory compliance, and data integrity. Their role involves coordinating with IT teams, lab staff, and external vendors to enhance system functionality and troubleshoot issues. Additionally, they may train users, manage system upgrades, and develop reports to improve operational efficiency.

What are the typical daily responsibilities of a lims manager?

As a Lims Manager, your daily responsibilities often include overseeing the configuration and maintenance of the LIMS to ensure it meets laboratory needs, managing user access, and providing technical support to lab staff. You may also coordinate with IT teams and laboratory personnel to implement system updates, ensure data integrity, and troubleshoot any system-related issues. Regular tasks can involve training users, generating reports for regulatory compliance, and optimizing workflows within the lab’s digital infrastructure. You'll play a key role in keeping laboratory operations streamlined, secure, and in alignment with industry standards.

What are the most commonly searched types of Lims jobs in Florida? The most popular types of Lims jobs in Florida are:
What are popular job titles related to Lims Manager jobs in Florida? For Lims Manager jobs in Florida, the most frequently searched job titles are:
What cities in Florida are hiring for Lims Manager jobs? Cities in Florida with the most Lims Manager job openings:
Infographic showing various Lims Manager job openings in Florida as of August 2026, with employment types broken down into 82% Full Time, 12% Part Time, and 6% Contract. Highlights an 100% In-person job distribution, with an average salary of $45,847 per year, or $22 per hour.

QA Validation Technician I

Kellton Tech

Tampa, FL • On-site

Contractor

Re-posted 25 days ago


Job description

Job Title: Quality Control (QC) Data Analyst / Chemist

Job Summary:
We are seeking a skilled and detail-oriented QC professional to support laboratory operations through hands-on testing, data transcription, analysis, and quality assurance in a cGMP-regulated environment. This individual will contribute to method development, validation, troubleshooting, and support project timelines while ensuring data integrity and regulatory compliance.


Key Responsibilities:

  • Execute practical laboratory work, including method development, method validation, and troubleshooting.

  • Perform quality control testing on raw materials, intermediates, and finished products to ensure compliance with specifications.

  • Support method technology transfer and project execution to ensure timely, smooth progression of QC-related deliverables.

  • Accurately transcribe laboratory data from worksheets, logbooks, and instrument outputs into electronic systems and official records in accordance with cGMP and data integrity requirements.

  • Analyze, trend, and review laboratory data for environmental, raw material, in-process, and final product testing.

  • Maintain and manage databases and electronic records, ensuring accuracy, traceability, and regulatory compliance.

  • Draft, revise, and review SOPs, protocols, and data review templates to support standardized data practices.

  • Collaborate with QC teams to investigate data deviations and support root cause analysis and CAPA implementation.

  • Generate data reports, summaries, and metrics for production support, audits, and continuous improvement initiatives.

  • Review GxP data for compliance with Good Documentation Practices (GDP) and regulatory protocols.

  • Support method and equipment validation through data compilation, statistical analysis, and reporting.

  • Prepare data packages for internal, client, and regulatory audits; respond to data-related inquiries.

  • Provide training and mentorship to QC personnel on data handling, transcription, and reporting procedures.

  • Assist in maintaining electronic lab systems (e.g., LIMS, CDS), ensuring data backup and access protocols are followed.

  • Identify data quality issues and facilitate timely resolutions through collaboration with stakeholders.

  • Maintain compliance with FDA, EPA, OSHA, and company-specific safety and regulatory guidelines.

  • Support company sustainability and safety programs by reporting hazards and halting unsafe practices when needed.

  • Perform additional tasks as assigned by QA Manager and/or QA Team Lead.


Qualifications:

  • Bachelor’s degree in Chemistry, Biochemistry, Microbiology, Life Sciences, or a related scientific discipline.

  • 2–4 years of experience in a cGMP-regulated laboratory environment, particularly in data transcription, analysis, or quality systems.

  • Proficiency in Microsoft Excel, statistical tools, and Laboratory Information Management Systems (LIMS).

  • Strong knowledge of cGMP, GDP, and data integrity principles.

  • Excellent attention to detail, organizational, and documentation skills.