Overview

A leading pharmaceutical company is seeking an experienced interim professional to support a short-term improvement project led by the Quality department. The role focuses on driving and completing defined improvement initiatives at the intersection of Quality and Operations within a GMP-regulated environment. The specialist will help structure ongoing initiatives, analyze current processes, and ensure implementation of operational and quality improvements together with internal teams.

Requirements

• Experience working in GMP-regulated environments.
• Professional experience in Quality and/or Operations within the life sciences, pharmaceutical, or biotechnology sector.
• Experience delivering project-based process improvement initiatives within an organizational setting.
• Experience working in cross-functional environments involving both Quality and Operations functions.

Desirable Qualifications

• Experience supporting short-term improvement or optimization projects within regulated manufacturing environments.
• Experience working within biopharmaceutical manufacturing organizations.
• Experience creating project structure, oversight frameworks, or implementation plans for operational improvements.
• Previous interim or freelance assignment experience within regulated life sciences environments.

Assignment Details

What the Assignment Offers: Interim assignment supporting Quality and Operations improvement initiatives within a GMP-regulated organization. Opportunity to contribute to defined improvement and optimization projects within a biopharmaceutical environment. Exposure to cross-functional collaboration between Quality and Operations teams. Short-term freelance assignment (approximately 3 months) with a clearly defined project scope. Opportunity to make a direct operational impact on internal improvement initiatives.

Contact

For a confidential discussion about this opportunity: Maurits van Sloun, [email protected], +31 20 204 4502