Analyst III

Piper Companies is looking for an Analyst III to join a pharmaceutical company located in Lansing, MI.

Responsibilities of the Analyst III include:

 · Support Empower system upgrade at Lansing site

· Coordinate and escort vendor during migration and upgrade activities

· Lead User Acceptance Testing (UAT) efforts

· Troubleshoot with vendor during IQ/OQ/PQ (Installation/Operational/Performance Qualification)

· Open archive files and ensure system validation (CSV), equipment validation, and analytical equipment readiness

Qualifications for the Analyst III include: 

· Demonstrated experience in Computer System Validation (CSV) in regulated environments

· Experience with analytical equipment validation (Empower experience not required)

· Ability to support and troubleshoot during IQ/OQ/PQ phases with external vendors

· Proven ability to lead or support UAT efforts ensuring systems meet functional and regulatory requirements

· Comfortable working in a secure lab setting and coordinating with third-party vendors

Compensation for Analyst III includes:

· Rate Range: $40–$50/hr

· Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law

This job is open for applications on August 22, 2025. Applications will be accepted at least 30 days from the posting date.

Keywords: Empower, Analyst III, chromatography data system, HPLC (High-Performance Liquid Chromatography), CSV (Computer System Validation), IQ/OQ/PQ (Installation Qualification / Operational Qualification / Performance Qualification), UAT (User Acceptance Testing), SOP (Standard Operating Procedure), GxP (Good Practice guidelines and regulations), FDA 21 CFR Part 11 (Food and Drug Administration Title 21 Code of Federal Regulations Part 11), LIMS (Laboratory Information Management System), CDS (Chromatography Data System), CAPA (Corrective and Preventive Action), system migration, software validation, equipment qualification, analytical instrumentation, lab systems, vendor coordination, data integrity, audit trail review, server upgrade, system architecture, validation protocols, technical documentation, remote access, centralized server, regulated environment, contract role, pharmaceutical IT, laboratory informatics, deviation management, change control, risk assessment, qualification protocols, validation master plan

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