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This role provides strategic and operational leadership across engineering and machine development, overseeing the conception, development, and deployment of advanced manufacturing technologies and equipment. The position is critical to enabling long term growth, competitiveness, and operational sustainability within a highly regulated environment.
This role leads the design, optimization and preclinical development of therapeutic peptides, PDCs and constrained macrocycles using structure-based and AI-driven drug design tools, while conducting SAR studies and cross-team collaboration to enhance candidate potency, druggability and binding performance.
Groupe industriel de premier plan, recherche un/une directeur de projet industriel sur site pharmaceutique H/F, pour une mission de management de transition d'une durée de 6 mois.
This is a senior leadership role for a seasoned chemical engineering professional who brings strong technical depth, proven project execution experience, and the ability to engage credibly with shareholders, partners, licensors, and EPC contractors.
Senior executive opportunity to build and lead the Quality function of a large greenfield manufacturing site within a global medical technology organization. This role will play a critical part in site start up, regulatory approval, and long term operational excellence, with a direct impact on patient safety worldwide.
This role is responsible for developing and implementing China-focused early clinical development strategies to generate high-quality, decision-driving data for global programs across genetic neurological, renal, pulmonary, and other rare genetic diseases.
You will lead translational research and early clinical development strategies, bridging discovery science with clinical application. The position combines scientific leadership, operational oversight, and regulatory engagement to accelerate innovative therapies toward commercialization.
A global MedTech organisation seeks a senior manufacturing leader to oversee a complex, regulated aseptic production environment. You will drive manufacturing strategy, operational performance, and organisational capability, managing manufacturing, engineering, and support functions while ensuring quality, compliance, and efficiency during a period of growth.
This role offers full ownership of Quality & Regulatory Affairs within an innovative, fast-growing MedTech company, combining strategic leadership with operational impact. You will work closely with international stakeholders while shaping regulatory strategy and ensuring compliance across a cutting-edge product portfolio.
The Director of Quality will report to the North America COO and lead a quality team of around 10-15 direct reports and a total team of 35-40. This includes Quality Managers, Supplier Quality, Auditor, Quality Customer Engineers, Quality Systems Managers, APQP and PPAP team and others.
We are seeking a Medical Director to join a leading international pharmaceutical organisation. While the role is designed to evolve into a Medical Director position, we are equally interested in high-potential candidates from Medical Affairs who may not yet hold this title but demonstrate the capability, ambition, and leadership potential to grow into the role over time, supported by a structured succession and development plan.
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