Temperature Mapping Validation Engineer — Contract

Novozen Healthcare LLC; Portland (OR); On-site; USD 69,000 - 83,000; Full time

Benefits offered by this job

Health Insurance

401(k) Retirement Plan

Paid Time Off (PTO)

Job summary

Novozen Healthcare LLC is seeking a Contract Validation Specialist to support qualification activities in GMP-regulated pharmaceutical environments in Portland, Oregon.

The role emphasizes temperature mapping, thermal validation, and CQ&Q execution with DeltaV, Historian, and electronic validation systems. You will prepare, review, and finalize documentation, ensure GMP compliance, and coordinate planning and on-site execution with remote support as needed.

Qualifications

• 5–8+ years of experience in validation and qualification within pharmaceutical or biotechnology industries.
• Strong hands-on experience in temperature mapping and thermal validation.
• Proven experience in Commissioning & Qualification (C&Q).
• Experience working in GMP-regulated environments.
• Familiarity with electronic validation execution systems.
• Knowledge of DeltaV and Historian systems.
• Preferred experience with eLab and ValGenesis.

Responsibilities

• Support temperature mapping planning, execution, and thermal validation activities within GMP-regulated environments.
• Prepare, review, and execute validation and qualification documentation.
• Ensure compliance with GMP requirements and applicable regulatory standards.
• Support activities involving DeltaV and Historian systems.
• Coordinate remote planning, documentation, and onsite execution activities as required.

Skills

Temperature mapping

Thermal validation

GMP compliance

C&Q experience

Electronic validation systems

Tools

DeltaV

Historian

eLab

ValGenesis

Job description

Novozen Healthcare LLC is seeking a Contract Validation Specialist to support qualification activities in GMP-regulated pharmaceutical environments in Portland, Oregon.

The role emphasizes temperature mapping, thermal validation, and CQ&Q execution with DeltaV, Historian, and electronic validation systems. You will prepare, review, and finalize documentation, ensure GMP compliance, and coordinate planning and on-site execution with remote support as needed.