Contract Role: CQV Expert (Commissioning, Qualification & Validation)

Location: Norway for 3.5 months, then fully remote.

Contract Duration: August - September 2026 for 6 months

Overview

A leading organization in the life sciences sector is seeking an experienced CQV Expert to support a brownfield aseptic manufacturing project in Norway. The successful candidate will play a key role in commissioning and qualifying both utilities and manufacturing equipment within Grade B and C cleanroom environments.

This position is due to start in the late summer of 2026 and is a 6 month project duration, with a high likelihood of extension.

Key Responsibilities

• Lead and execute commissioning, qualification, and validation (CQV) activities for black and clean utilities.
• Manage CQV for aseptic manufacturing equipment, including tray loaders in CNC environments.
• Coordinate scheduling and progress tracking for larger line commissioning activities.
• Support validation planning and documentation to meet project and regulatory requirements.
• Collaborate with cross-functional teams to ensure seamless project execution.

Requirements

• Proven experience with brownfield CQV projects in aseptic or sterile manufacturing environments.
• Strong background in utility systems (both black and clean) and manufacturing equipment qualification.
• Expertise in scheduling, commissioning management, and validation documentation.
• Availability to be on-site in Norway for approximately 2.5–3.5 months during the commissioning and qualification phase.
• German and English fluency is mandatory.