Role Purpose Client facing role owning solution and transformation narrative across Pharma late stage R&D and Drug Development in Capgemini NCE SBU. The role focuses on shaping large-scale R&D and clinical transformation deals, enabling clients to accelerate innovation,
Development Manager II, Large Molecules D&M ADS Licensing Location: Oss The Development Manager leads and coordinates the end-to-end development of GlycoConnect and other components, from early-stage research through process scale-up and commercial manufacturing. Independently manage technology components, vendors and
Senior research associate Analytical Development Location: Oss As a result of the increasing number of external ADC collaborations, we are currently looking for a skilled and enthusiastic Senior Research Associate Analytical Development Bioconjugates. You will operate as an
Position Overview: As a Senior Software Engineer, you are responsible for driving the design, development, and scalability of our Third Party Risk Management (SaaS) platform built on Laravel (PHP). You play a key role in building new
General Information Job Advert Title Associate Director Risk Management Location Netherlands Function/Business Area Product Safety Employment Class Permanent Description Associate Director Risk Management About Astellas Astellas is a global life sciences company committed to turning innovative
https://www.dekra.nl/nl/home/ solliciteren What will your role involve The Medical division is a leading and fast-growing Notified Body within the Medical Device Industry. Consequently, we are consistently looking for medical auditors or technical file reviewers. Dealing with
Job Purpose: Code of practice for promotion and scientific engagement: Delivering and exchange of information within the medical dialogue with the external environment. The non-promotional interaction and exchange of information between GSK and external communities in
About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScripts businesses encompass four
About Ardena Ardena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development. Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex molecules from discovery to market. The
Regulatory Affairs Specialist Location: Oss The Regulatory Affairs (RA) Specialist within the Development & Manufacturing department, ADS Licensing, is responsible for the preparation, review, and maintenance of high-quality regulatory submission documents describing the chemistry, manufacturing, and controls
Position Overview: Diligent is looking for a talented QA Analyst to improve the quality of Diligent products. The QA Analyst is part of a cross-functional agile team and involved in every step of the software testing
Introduction to Ardena Ardena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development. Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex molecules from discovery to market.
Job Title: Business Development Lead– Antibody Licensing Location: Netherlands Company: US-based Biotech (via Talentmark) Talentmark is partnering with a fast-growing, US-headquartered biotech at the forefront of antibody discovery and development. With cutting-edge platforms and a strong global footprint,