LIMS & Master Data Analyst — Pharma Data Integrity

ManpowerGroup; Swiftwater (Monroe County); On-site; USD 83,000 - 110,000; Full time

Benefits offered by this job

Medical Plan

Dental Plan

Vision Plan

HSA

FSA

Dependent Care FSA

Life Insurance

STD/LTD Insurance

Travel Insurance

401(k) Match

Weekly Pay

Job summary

ManpowerGroup is seeking a USA-Process & Master Data Governance Manager I (Professional) to join its Quality Operations team in Swiftwater, PA. You will support data integrity and master data management initiatives in a pharmaceutical setting.

Responsibilities include maintaining the LIMS, updating product master data, ensuring compliance with cGMPs and 21 CFR Part 11, and contributing to training materials.

Qualifications

• 1-3 years of hands-on experience with LabWare LIMS administration and basic system management.
• Strong knowledge of laboratory processes, cGMPs, and regulatory requirements in a pharmaceutical environment.
• Experience with master data management, system validation, and data integrity best practices.
• Familiarity with SQL and database structures is preferred.
• Excellent written and verbal communication skills, with the ability to lead and collaborate within teams.

Responsibilities

• Support LIMS maintenance and improvement to ensure data accuracy and compliance.
• Update master data for products, sample plans, and item codes to support remediation and SPC projects.
• Ensure LIMS compliance with cGMPs and 21 CFR Part 11.
• Create and update training materials for system changes and data management.
• Collaborate with cross-functional teams on validation, data migration, and SOP revisions.

Skills

LIMS administration

cGMPs

Master data management

Data integrity

SQL

Tools

SQL

Job description

ManpowerGroup is seeking a USA-Process & Master Data Governance Manager I (Professional) to join its Quality Operations team in Swiftwater, PA. You will support data integrity and master data management initiatives in a pharmaceutical setting.

Responsibilities include maintaining the LIMS, updating product master data, ensuring compliance with cGMPs and 21 CFR Part 11, and contributing to training materials.