Validation Specialist Jobs

QRC Group is hiring a CSV Specialist with bioprocess validation expertise to execute commissioning, qualification and computerized system validation across manufacturing and laboratory environments.

Validation & Engineering Group is looking for a bilingual Computer Systems Validation Specialist to lead lab equipment CSV activities, author and execute IQ/OQ/PQ protocols, and ensure cGxP-compliant data integrity for pharmaceutical and biotech clients.

QRC Group is hiring a bilingual Quality Systems Documentation Specialist to manage and maintain regulatory documentation and support validation activities at its Vega Baja, PR location.

Lumafield is hiring a Regulatory Affairs Specialist to define and execute regulatory strategy and compliance processes for its industrial CT hardware-software products.

Experienced analytical instrumentation specialist needed to lead validation, qualification, and method transfers for QC instruments in a regulated life-sciences environment.

An experienced HRIS specialist is needed to lead Workday configuration, integrations, and reporting to support People Technology and analytics across the firm.

Carnegie Mellon University is hiring a Global Payroll Specialist to support accurate gross-to-net payroll processing, non-resident alien treaty administration, and payroll case management for a multi-state, international higher-education environment.

Legal & General Retirement America is hiring a Benefit Calculation Specialist to deliver accurate pension benefit calculations, support system validations and onboarding, and drive process improvements across Retirement Services.

Experienced engineering technician to support equipment optimization, MAXIMO data maintenance, and regulatory-compliant maintenance operations for a pharma/medical device consulting client.

QRC Group is hiring a Specialist QA in Juncos, Puerto Rico to lead validation, commissioning/qualifications and quality system activities for manufacturing operations.

QRC Group seeks an experienced Quality Systems Specialist to manage and improve quality systems, support investigations, and ensure compliance with GMP, FDA 21 CFR Part 11 and data integrity requirements.

Quality Assurance Specialist needed at Catalent's Kansas City biologics analytical center to conduct lab and document audits, approve analytical documents, and support GxP compliance.

GRAIL is hiring a Staff Quality Systems Specialist in Durham, NC to manage and improve eQMS-driven document control, records management, and training programs (Veeva experience highly preferred).

Kincell Bio seeks a detail-oriented Manufacturing Specialist to support on-site cGMP cell therapy production, operate automated and manual equipment, and manage GMP documentation and corrective actions.

Experienced QA Specialist needed to perform cGMP document reviews, batch and lab data release, audits, and investigations for Lonza's Tampa manufacturing site on the 3–11 PM shift.