About the role

Laboratory Informatics Consultant implementing and supporting LIMS solutions in pharmaceutical and biotech environments. Designing and deploying informatics solutions to improve data integrity and compliance.

Responsibilities

Work with pharmaceutical, biotech, CRO, and regulated laboratory environments to design, configure, and deploy LIMS solutions
Support sample lifecycle in regulated laboratory environments
Operate independently on medium-complexity projects and collaborate with global support team
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 independently or as part of a team
Develop and execute system testing and validation deliverables
Support user acceptance testing and defect resolution
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

3+ years of experience working with laboratory informatics systems such as LabWare, LabVantage, or similar LIMS platforms
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
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)

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 superior benefits to those outlined by law, a competitive compensation package including accrued vacation, and a healthy Christmas bonus.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo Mexico 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.