LIMS Master Data Analyst

Manpower Group (USA); Swiftwater (Monroe County); On-site; USD 83,000 - 112,000; Full time

Job summary

USA-Process & Master Data Governance Manager I (Professional) at a leading pharmaceutical organization in the Quality Operations department in Swiftwater, PA. You will support data integrity and master data management initiatives, leveraging strong analytical and collaborative skills.

Key duties include maintaining LIMS, updating master data for products and codes, ensuring compliance with cGMPs and 21 CFR Part 11, and supporting system validation and data migrations.

Qualifications

• 1–3 years of hands-on LabWare LIMS administration.
• Strong knowledge of cGMPs and 21 CFR Part 11 in pharma.
• Experience with master data management and data integrity.
• Familiarity with SQL and database structures.
• Excellent written and verbal communication; capable of leading teams.

Responsibilities

• Support LIMS maintenance and data accuracy within QO.
• Assist in updating master data for products and item codes.
• Ensure regulatory compliance across systems.
• Contribute to training materials on data management.
• Collaborate on system validation and data migrations.

Skills

LIMS administration

Master data governance

SQL knowledge

Regulatory compliance

Team collaboration

Data integrity

Tools

LabWare LIMS

Job description

Our client, a leading organization in the pharmaceutical and life sciences industry, is seeking a USA-Process & Master Data Governance Manager I (Professional) to join their team. As a USA-Process & Master Data Governance Manager I (Professional), you will be part of the Quality Operations department supporting data integrity and master data management initiatives. The ideal candidate will demonstrate strong analytical skills, effective communication, and a collaborative mindset, which will align successfully within the organization.

Job Title: USA-Process & Master Data Governance Manager I (Professional)

Location: Swiftwater, PA

Pay Range:$70.19

What's the Job?

• Support the maintenance and improvement of the Laboratory Information Management System (LIMS) to ensure data accuracy and compliance.
• Assist in updating master data for products, sample plans, and item codes to support data remediation and SPC projects.
• Ensure the LIMS system complies with all relevant regulatory standards, including cGMPs and 21CFR Part 11.
• Contribute to the creation and updating of training materials related to system changes and data management processes.
• Collaborate with cross-functional teams to support system validation, data migration, and SOP revisions.

What's Needed?

• 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.

What's in it for me?

• Opportunity to work in a dynamic and impactful industry focused on health and well-being.
• Engage in meaningful projects that support regulatory compliance and data integrity.
• Collaborate with a diverse and talented team committed to excellence.
• Gain valuable experience in laboratory information systems and master data governance.
• Be part of an organization that values innovation, integrity, and continuous improvement.

Upon completion of waiting period, consultants are eligible for:

• Medical and Prescription Drug Plans
• Vision Plan
• Health Savings Account
• Health Flexible Spending Account
• Dependent Care Flexible Spending Account
• Supplemental Life Insurance
• Short Term and Long Term Disability Insurance
• Business Travel Insurance
• Weekly Pay