Top 50 Labvantage lims Jobs

LIMS Analyst (LabVantage)
Zifo —Boston, MA
- Mid-level
- 3 years
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Labvantage LIMS Support Engineer
Capgemini —Cincinnati, OH
- $73,150 - $174,000 a year
- Full-time
- Mid-level
- SQL
- Bachelor's degree
- Paid holidays
- Disability insurance
5d
QC Systems Engineer IV (LabVantage LIMS)
Resilience US, LLC —West Chester, OH
- $90,000 - $153,750 a year
- Full-time
- 5 years
- SQL
- Analysis skills
- Paid holidays
- Disability insurance
Quick Apply
Senior Software Engineer, LIMS (Hybrid)
NeoGenomics Laboratories —Ramsey, NJ
- Hybrid work
- Computer science
- 7 years
- Azure
- Employee stock purchase plan
- Paid holidays
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Senior Quality Control Analyst I, Bioassay
Ultragenyx Pharmaceutical —Woburn, MA
- $101,500 - $125,400 a year
- Full-time
- Bachelor of Science
- Ability to climb stairs
- Ability to lift 50 pounds
- Gym membership
6d
Principal System Engineer LIMS
Moderna, Inc. —Norwood, MA
- $130,800 - $209,400 a year
- Full-time
- Remote
- System design
- Bachelor's degree
- Experience equivalent to degree accepted
- Paid time off
- Adoption assistance
9d
LIMS Implementation Coordinator (Contract)
Kashiv BioSciences, LLC —Chicago, IL
- $65 - $75 an hour
- Extended hours
- Mid-level
- Master's degree
- Travel
Laboratory Assistant
Asklepios BioPharmaceutical —Durham, NC
- Full-time
- Microsoft Excel
- Mid-level
- High school diploma or GED
Laboratory Systems Analyst (ELN/LIMS)
Westbourne IT Global Services —La Verne, CA
- $12.50 - $19.50 an hour
- Full-time
- Hybrid work
- Computer Science
- Mid-level
- 3 years
- Opportunities for advancement
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Sr. Associate-Global Lab Informatics (LIMS)
Elanco —Indianapolis, IN
- Full-time
- Laboratory experience
- Mid-level
- 3 years
Laboratory Analyst
Philip Morris International U.S. —Aurora, CO
- $88,000 - $110,000 a year
- Full-time
- English
- Mid-level
- 3 years
- Profit sharing
- Paid jury duty
QC Data Senior Specialist
CooperSurgical —Livingston, NJ
- $105,000 - $115,000 a year
- Full-time
- Azure
- Master's degree
- AWS
- Health insurance
- Paid time off
Scientist II, Analytical Development, Gene Editing and Molecular Assays
Legend Biotech US —Somerset, NJ
- $110,706 - $145,303 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
Data Analyst - Biorepository Operations
City of Hope —Duarte, CA
- $37.11 - $57.52 an hour
- Full-time
- Computer Science
- System design
- Mid-level
Laboratory Informatics Analyst
Quanterix —Bedford, MA
- $100,000 - $120,000 a year
- Hybrid work
- Computer Science
- 5 years
- Mid-level
- Employee stock purchase plan
- Dental insurance
6d
Sr. Principal Chemist
Eli Lilly —Concord, NC
- $65,250 - $169,400 a year
- Full-time
- Continuous improvement
- Mentoring
- In-person
- Health insurance
- Dental insurance
12d
Quality Control Specialist, Master Data Builder (Contract)
Rentschler Biopharma SE —Milford, MA
- Contract
- Microsoft Excel
- 5 years
- Mid-level
IT Business Systems Analyst - Pharma Applications
Virbac —Bridgeton, MO
- Full-time
- Master's degree
- SQL
- Bachelor's degree
Senior Manufacturing Engineer
GeneFab —Alameda, CA
- $72 - $86 an hour
- Full-time
- Engineering
- 3 years
- Doctor of Philosophy
Quick Apply
Quality Systems Engineer
Cytiva —Logan, UT
- Full-time
- Oracle
- 5 years
- Laboratory experience

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LIMS Analyst (LabVantage)

Zifo
Boston, MA

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Job Details

Benefits

Health insurance
Dental insurance
Flexible spending account
Vision insurance
401(k) matching
Life insurance

Qualifications

Data integrity assurance
Feature validation testing
Data compliance
Requirements specification
Requirements design
GxP
Test Case Documentation (Quality assurance practices)
Technical documentation
Pharmaceutical regulatory compliance
Testing and evaluation
Software implementation
Enterprise solutions implementation
Application deployment
Improving operational efficiency
User training (technical support)
Data integrity and documentation
Production systems
Bachelor's degree
User support
User acceptance testing
Chain of custody
System deployment
Laboratory information systems (LIS)
Analysis (software development lifecycle)
Test validation method
Implementing IT solutions
Project stakeholder communication
Validation design
Laboratory compliance and regulatory documentation
Sample accessioning

Full Job Description

Other locations: San Francisco Bay Area, Tri-state Area (NY, NJ, PA), RTP (NC)

We are seeking a Laboratory Informatics Consultant with hands-on experience implementing and supporting enterprise LIMS platforms such as LabWare, LabVantage, or similar systems. This role is focused on delivering sample‑centric LIMS solutions, supporting the full sample lifecycle in regulated laboratory environments. Consultants in this role are expected to be able to operate independently on medium-complexity projects as well as collaborating with a global support team on larger projects.

As a consultant on our team, you will work with pharmaceutical, biotech, CRO, and regulated laboratory environments to design, configure, and deploy informatics solutions that improve data integrity, compliance, and operational efficiency. The ideal candidate understands how laboratories operate day to day and can design LIMS solutions that support compliant, efficient, and traceable laboratory workflows, while also configuring supporting entities such as instruments and inventory as needed.

Requirements

Lead or support requirements gathering with laboratory stakeholders, emphasizing end‑to‑end sample lifecycle management
Analyze laboratory processes related to sample receipt, testing, review, approval, and disposition
Translate business and regulatory requirements into LIMS functional designs and configuration specifications
Configure LIMS solutions ( LabVantage) independently or as part of a national or global team to support:

- Sample login, accessioning, and chain of custody
- Test assignment, execution, calculations, and result entry
- Specifications, limits, and result evaluation
- Review, approval, release, and reporting workflows
Configure supporting LIMS entities required for sample workflows, including tests, methods, materials, products, and locations
Configure instrument and inventory data as required to support compliant sample testing

Develop and execute system testing and validation deliverables (IQ/OQ/PQ, test scripts, traceability matrices)
Support user acceptance testing and defect resolution
Assist with production deployment and go‑live activities

Provide post‑implementation support focused on sample processing, results management, and workflow execution
Troubleshoot issues impacting sample lifecycle workflows and data integrity
Deliver end‑user training and documentation
Identify opportunities to improve efficiency, compliance, and usability within the LIMS

Required Qualifications

3+ years of experience working with laboratory informatics systems LabVantage.
Strong experience implementing and supporting sample lifecycle management in LIMS
Solid understanding of laboratory workflows (QC, analytical, stability, manufacturing, or R\&D)
Experience working in regulated environments (GxP, FDA, ISO; ALCOA+ principles)
Strong communication skills and experience working directly with laboratory and QA stakeholders
Bachelor’s degree in a scientific, technical, or related field

Preferred Qualifications

Hands-on laboratory experience or a background in chemistry or biology
Experience with complex sample models (e.g., stability programs, high‑volume QC, or multi‑site labs)
System validation and CSV documentation experience
Exposure to LIMS integrations or configuration scripting
Consulting or client‑facing experience
Experience supporting instrument or inventory data in the context of sample workflows, rather than asset‑centric implementations
Experience working across multiple informatics systems (e.g., LIMS, ELN, CDS, SDMS)

Benefits

CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 18 of the Top 20 Biopharma companies.

We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.

We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.

If you share these sentiments and are prepared for the atypical, then Zifo is your calling!

Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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