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Manager Program Management
Brussels$180,000 USD a year

Manager, Program ManagementLocation: Madison, WI Work Model: 100% Onsite Compensation: Competitive base salary + bonus potential + comprehensive benefitsAbout the OpportunityAn expanding biologics CDMO is seeking a Manager of Program Management to lead complex client programs across biologics development and manufacturing. This individual will over...

External Quality Senior Specialist
Beerse€50 - €70 EUR a day

Our client is seeking an experienced External Quality Senior Specialist to support Quality Process & Operations activities within a global pharmaceutical environment. This role focuses on strengthening External Quality processes, supplier oversight, quality systems management, regulatory compliance, and continuous improvement initiatives across ex...

Clinical Fair Market Value Analyst
Diegem

Clinical Budget & Fair Market Value AnalystWarsaw, Poland | Hybrid (3 days onsite per week) We are currently supporting a global life sciences organisation looking to hire a Clinical Budget & Fair Market Value Analyst to join their clinical operations team in Warsaw.This is a fantastic opportunity for someone with experience in clinical research an...

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Senior Application Engineer
LeuvenNegotiable

Senior Applications Engineer - Semiconductor TechnologyLocation: Leuven, BelgiumWe are supporting an innovative semiconductor technology company looking to hire a Senior Applications Engineer to join a major joint development programme with a leading European semiconductor research organisation.This is a highly customer-facing, technical position c...

Asset CQV Engineer
GhentNegotiable

Asset Engineer (CQV) - Ghent, Belgium (Fully Onsite)OverviewWe are seeking an experienced Asset Engineer (Commissioning, Qualification & Validation) to join a leading pharmaceutical manufacturing facility in Ghent, Belgium. This position is responsible for ensuring manufacturing equipment, utilities, and systems remain qualified, compliant, and in ...

Regulatory Specialist
BrusselsNegotiable

Regulatory Affairs Specialist - Medical Devices Location: Belgium (Hybrid)Industry: Medical Devices / Medical Equipment Manufacturing About the Role An established international medical device organisation is seeking a Regulatory Affairs Specialist to support regulatory market access, product lifecycle management, and compliance activities across ...