LIMS Master Data Lead: GMP Compliance

Hartmann Young; New York (NY); On-site; USD 65,000 - 95,000; Full time

Job summary

Hartmann Young in New York seeks a GMP-compliant LIMS data specialist to create and revise master data elements in the LIMS platform, including test methods, specifications, sampling plans, product parameters and instrument mappings.

You will enforce data integrity, assist with data migration and validation, and collaborate with QA/QC, IT and SMEs to map workflows and implement new functionality, while supporting audits and SOPs.

Qualifications

• 2–5 years of experience in a GMP-regulated pharmaceutical or life sciences lab.
• Experience with LIMS platforms as an end user or in LIMS implementation.
• Understanding of analytical testing and techniques.

Responsibilities

• Create and revise master data elements in LIMS (test methods, specifications, analytical procedures, sampling plans, product parameters, instrument mapping).
• Enforce data integrity, version control, and data accuracy across laboratory processes; ensure compliance with FDA 21 CFR Part 11, cGMP, ISO 17025.

Skills

LIMS data management

Data integrity

Regulatory compliance

Analytical understanding

Cross-functional collaboration

Education

Associate’s or Bachelor’s degree in Life Sciences/Engineering

Tools

LIMS software

Job description

Hartmann Young in New York seeks a GMP-compliant LIMS data specialist to create and revise master data elements in the LIMS platform, including test methods, specifications, sampling plans, product parameters and instrument mappings.

You will enforce data integrity, assist with data migration and validation, and collaborate with QA/QC, IT and SMEs to map workflows and implement new functionality, while supporting audits and SOPs.