Quality Auditor

Start Date: as soon as possible

End Date: 31 December 2025

Extension: possible

Engagement: 100%

Location: Hybrid (3 days/week onsite)

Department Overview

The Clinical Supplies Quality team is responsible for ensuring the compliant release of both clinical and commercial drug products. This includes the review and approval of incoming label stock, packaging materials, and final labeled products used in clinical trials.

Key Responsibilities

• Review and release of incoming label stock
• GMP-compliant review of batch records and printed/applied labels
• Final release of clinical finished goods
• Review of regulatory filings as part of the release process

Candidate Requirements

• Minimum 3 years of experience in a Quality Assurance role, including:
• Batch record review
• Deviation and change management
• SOP review and compliance oversight
• Experience may come from clinical or commercial pharmaceutical or medtech environments
• Bachelor’s degree in a relevant scientific or technical field is mandatory
• Candidates without a bachelor's degree will not be considered
• Candidates with a PhD and over 10 years of experience may be considered overqualified
• Must reside within a reasonable commuting distance to allow 3 on-site working days per week

Work Environment

This is a hybrid role. The successful candidate will start fully onsite during the training period, and transition to a hybrid setup (currently 2 days onsite / 3 days remote), subject to change based on business needs.

Are you interested in a new role in Quality Systems and ready to support clinical excellence? Apply now and take the next step in your career!