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Our client, a prominent pharmaceutical organization, is seeking a professional to provide strategic pricing leadership for early-stage candidates and pipeline solutions. The role focuses on translating payer and health-system requirements into robust pricing strategies and evidence expectations to support key development decisions.

Our client, a leading life sciences organization, is seeking an expert to oversee validation activities for transport and CMO-manufactured products. This role ensures the compliance of validation lifecycles, protocols, and risk assessments while serving as a key technical point of contact for regulatory submissions and audits.

Our client, a leading global pharmaceutical organization, is seeking a Dissolution Scientist to support the development of innovative medication. This role focuses on designing dissolution strategies and applying biopharmaceutical assessments to predict drug release rates and optimize formulations.

Chez Pauwels Consulting, nous recherchons un Project Coordinator pour l'un de nos clients, un acteur majeur de l'industrie pharmaceutique et des vaccins en Belgique.

Le client transfère ses activités de laboratoire vers un nouveau site. De nombreux équipements restent dans l'ancien bâtiment : obsolètes, redondants ou devenus inutiles. Vous pilotez leur decommissioning de bout en bout, dans le respect des procédures qualité et EHS. L'objectif est de libérer et remettre en état les espaces pour le département QC.

Our client, a leading biopharmaceutical organization, is seeking an expert to drive analytical excellence within their manufacturing science and technology department. This role focuses on developing and implementing critical analytical methods to ensure the quality and consistency of cell culture-based production processes across an international biologics network.

At Pauwels Consulting, we connect talented scientists with projects that matter. For one of our clients, a leading global biopharmaceutical company, we're looking for you to join the Analytical Science and Technology (AST) team at their state-of-the-art biologics facility in the Kempen region.

The team is part of the client's global Manufacturing Science, Analytics and Technology (MSAT) organization. You'll develop and implement critical analytical methods that safeguard the quality and consistency of mammalian cell culture processes across an international biologics network.

The pipeline is impressive: more than 20 innovative therapies are set to reach patients in the next 3–5 years. Think monoclonal antibodies, fusion proteins, ADCs, synthorins and nanobodies. The portfolio spans multiple products, modalities and expression systems, at internal and external sites across the US and Europe.

Your work directly supports successful product launches and manufacturing excellence. You'll grow your expertise in a collaborative, scientifically stimulating environment at the leading edge of biopharma. And you'll have the full support of Pauwels Consulting behind you, every step of the way.

Our client, a prominent pharmaceutical organization, is seeking a CAR-T QA C&Q Engineer to support their innovative manufacturing operations. This role is responsible for the oversight and approval of qualification activities for facilities, utilities, and process equipment within a specialized therapeutic environment.

Onze klant, een internationale organisatie binnen de productiesector, is op zoek naar een ervaren consultant ter versterking van het kwaliteitsteam. De focus van deze rol ligt op het waarborgen van de hygiënische standaarden en het ondersteunen van de operationele afdelingen op de site.

Our client, a leading pharmaceutical organization, is seeking a dedicated professional to provide quality oversight for site facilities and utilities. This role focuses on ensuring compliance across the system lifecycle, from initial design through to ongoing maintenance and decommissioning.

Our client, a leading MedTech organization, is seeking a Clinical Research Associate to manage clinical activities across various study sites. The role focuses on overseeing site performance, conducting monitoring visits, and ensuring the delivery of high-quality data for clinical projects.

Our client, a leading player in the MedTech industry, is seeking a Senior Clinical Research Associate to manage clinical study activities across multiple sites. This role focuses on overseeing study site performance, conducting comprehensive monitoring visits, and ensuring high-quality data collection for various medical device projects.

Our client, a leading life sciences organization, is seeking an expert to lead comprehensive regulatory dossier assessments and file gap analyses. The project focuses on identifying compliance risks and developing scientific justifications to support regulatory submissions and health authority responses.