LabVantage LIMS / Master Data Specialist

Unicon Pharma Inc; Portsmouth (NH); On-site; USD 90,000 - 120,000; Full time

Job summary

Unicon Pharma Inc. is seeking an experienced LabVantage LIMS / Master Data Specialist to support QC master data setup, data migration, cleansing, and loading into a global LIMS environment.

Responsibilities include configuring, loading, and maintaining QC master data in LabVantage LIMS/gLIMS, managing consumables, sampling plans, specifications, parameters, test methods, and LES templates, and performing data cleansing and quality checks.

Qualifications

• Experience in LIMS/QC/Pharma/Biotech environments.
• Hands-on LabVantage or similar LIMS experience.
• Experience with master data management, migration and cleansing.
• GMP knowledge and data integrity understanding.
• Excellent analytical, documentation, communication and problem solving.

Responsibilities

• Configure, load, and maintain QC master data in LabVantage LIMS/gLIMS.
• Manage consumables, sampling plans, specifications, parameters, test methods, and LES templates.
• Perform data cleansing, validation, reconciliation, and quality checks.
• Develop site-level SOPs/work instructions.
• Support LIMS implementation, data migration, validation, and go-live activities.
• Collaborate with QC, QA, IT, Manufacturing, and Validation teams.
• Ensure compliance with GMP, GxP, data integrity, and regulatory requirements.

Skills

LabVantage LIMS

Master data management

Data cleansing

GMP knowledge

QC laboratory operations

Documentation

Communication

Tools

LabVantage or similar LIMS

TrackWise/QMS

Job description

Title: LabVantage LIMS / Master Data Specialist

Locations: Portsmouth, NH | Houston, TX

Summary

We are seeking an experienced LabVantage LIMS / Master Data Specialist to support QC laboratory master data setup, data migration, cleansing, and loading into a global LIMS environment.

Key Responsibilities

• Configure, load, and maintain QC master data in LabVantage LIMS/gLIMS.
• Manage consumables, sampling plans, specifications, parameters, test methods, and LES templates.
• Perform data cleansing, validation, reconciliation, and quality checks.
• Develop site-level SOPs/work instructions.
• Support LIMS implementation, data migration, validation, and go-live activities.
• Collaborate with QC, QA, IT, Manufacturing, and Validation teams.
• Ensure compliance with GMP, GxP, data integrity, and regulatory requirements.

Required Skills

• Experience in LIMS/QC/Pharma/Biotech environments.
• Strong hands-on experience with LabVantage or similar LIMS.
• Experience with master data management, data migration, and data cleansing.
• Strong knowledge of QC laboratory operations and GMP.
• Experience with LES, CSV, TrackWise/QMS is a plus.
• Excellent analytical, documentation, communication, and problem-solving skills.