Offer summary

Qualifications:

Proven experience implementing Labware LIMS in pharmaceutical environments., Proficiency in LIMSBasic scripting and Crystal Reports development., Strong understanding of Labware's relational database structure., Minimum 3 years of experience in regulated pharmaceutical environments..

Key responsibilities:

Configure and customize Labware LIMS using LIMS Basic scripting language.

Design and modify Crystal Reports for specific workflows.

Develop and maintain site-specific Master Data aligned with quality and manufacturing processes.

Collaborate with cross-functional teams to ensure effective system utilization.

Katalyst Healthcare's & Life Sciences (Katalyst HLS) is a Global Contract Research Organisation that provides End-to-End Clinical Research Services for Healthcare and Life Sciences companies globally. At Katalyst HLS offers ICH-GCP compliant clinical trial services from Phase I–IV in all key therapeutic areas to support clinical development and research requirements and also provides validation, quality and regulatory services for Pharma/Bio-Pharma/Medical Device industries. Services:- Clinical Trial Management- Clinical Data Management- Biostatistics & Statistical Programming- Medical Writing- Pharmacovigilance- Quality and Regulatory Affairs- GMP, GLP and GCP Validations- Manufacturing Process Validations- Equipments & Instruments Validations- Computer Systems Validations- Human Resourcing

Job description

Job Description:
We are seeking a skilled Labware LIMS Consultant to support Labware configuration, reporting, and master data development for a leading pharmaceutical and consumer packaged goods (Client) organization. This is a fully remote role.
Responsibilities:

Configure and customize Labware LIMS using LIMS Basic scripting language.
Design, build, and modify Crystal Reports tailored to Client and pharma-specific workflows.
Leverage deep understanding of Labware database structures to support integration, reporting, and data analysis needs.
Develop and maintain site-specific Master Data aligned with quality, R&D, and manufacturing processes.
Ensure configurations align with industry best practices and the Labware Pharma Template.
Collaborate with cross-functional teams including IT, QA, QC, and business users to ensure effective system utilization.

Requirements:

Proven experience implementing Labware LIMS, preferably in both pharmaceutical and Client environments.
Proficiency in LIMSBasic scripting and Crystal Reports development.
Strong understanding of Labware's relational database structure and data modeling.
Hands-on experience building and managing Labware Master Data.
Minimum 3 years of experience in regulated pharmaceutical or Client environments, with knowledge of the Labware Pharma Template.