Technical Validation Jobs

Palo Alto Networks seeks an experienced Solutions Consultant to provide pre-sales technical leadership, design cross-platform security solutions, and drive customer adoption for SLED accounts.

At Elanco's Winslow manufacturing site, the Quality Assurance Associate will ensure product and process quality by managing deviations, supporting batch disposition, and driving compliance across operations.

A hands-on entry-level engineering role at AbbVie supporting small projects, compliance, testing, and process design within a collaborative pharmaceutical environment.

Experienced engineer with protein purification and strong technical writing skills needed to support validation and process improvement projects at a regulatory-focused services firm in Juncos, PR.

Lead the product definition and global deployment strategy for L4 autonomous driving features at WeRide.ai, partnering closely with engineering, operations, and regulators.

Lead cross-functional programs for battery cell development at GM by coordinating design, process readiness, validation, and stakeholder communications to deliver development and scaled batch builds.

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.

UChicago Medicine is hiring a Technical Lead in Clinical Chemistry to drive method implementation, ensure high-quality testing, and lead technical staff at its Hyde Park laboratory.

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.

QRC Group is hiring a bilingual Technical Writer in Gurabo to produce and maintain GMP- and regulatory-compliant documentation supporting pharmaceutical development, manufacturing, and inspections.

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

Experienced technical project manager needed to lead biologics manufacturing transfers, investigations, and continuous improvement initiatives at Zoetis' Charles City facility.

AbbVie seeks a Principal Engineer to lead cleaning validation and process support for oral solid dosage manufacturing, ensuring reliable commercial production and compliance.

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

Technical Program Manager to lead cross-functional hardware and software programs at Tenstorrent, driving schedules, risks, and cross-team alignment for high-performance AI products.

QRC Group seeks a Specialist Tech Engineering in Juncos to support equipment optimization and maintenance compliance for regulated pharmaceutical/medical device environments.

Experienced QA professional needed to lead technical document reviews, investigations, and validation oversight at Catalent's St. Petersburg soft-gel manufacturing site.

Experienced Process Development Scientist needed to lead vision-system-based equipment characterization and validation activities for a regulatory-focused services firm supporting pharmaceutical and medical device clients.