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Scientific Consultant (project position) – DTU Health Tech
DTU Health Tech is seeking a formulation chemist to contribute to an exciting local depot formulation technology, CarboCell, e.g. for delivery of antibiotics aimed at local infection treatment.
This role is a unique blend of scientific research and commercial venture, involving work on patented technologies and a strategy for sustained release of small molecule-based therapies.
You will play a key role in evolving our research into a successful spin-out company.
Test & Reliability Engineer - Sustaining Engineering, Medical Devices
Do you have a keen eye for Physical Testing, Product Quality, Reliability, Validation, and Documentation? Are you looking for an opportunity to merge your passion with our expertise in the Test and Verification of Infusion Care Medical Devices, for the treatment of chronic diseases such as Diabetes and Parkinson’s Disease?
As a Test Engineer, you will be involved in developing and working with a diversity of physical test methods. Planning and coordinating tests in our laboratory in Osted near Roskilde, and partners within Global Convatec and external. Most of your time, you will be part of a project team in SEG.
Senior Vice President, Global Chief Medical Office
We are seeking a highly experienced and dynamic medical executive to join our Global Research & Development organisation in a newly established senior leadership role as SVP, Global Chief Medical Office (GCMO).
In this role, you will act as scientific advisor to the EVP of R&D and the Global R&D leadership team, and your primary objective will be to ensure “one global medical voice” for ALK internally and represent the medical voice of ALK externally.
Validation Engineer
As our new Validation Engineer, you will be responsible for validation and qualification of processes and equipment related to customer projects.
Key responsibilities in this role include, but are not limited to:
- Validation and Qualification of processes and equipment when implementing new material.
- Perform Validation and ensure results are accurately documented.
Application Technician – Food Ingredients
We are looking for an employee with an interest in laboratory and food technology to assist in the AKV FoodLab in Aarhus, where you will become part of the team.
Here you will play an important role in relation to taking part in the ongoing laboratory work with a confident and collaborative team approach.
As an Application Technician in AKV FoodLab, your primary tasks will consist of:
- To assist the Senior Application Specialist with research by running trials of a broad range of applications in the FoodLab and conducting analysis and characterization of food products.
- Maintenance and cleaning of process equipment.
- Contribute where required in purchasing tasks for the FoodLab.
Associate Sensory scientist/Sensory Panel Lead - Arla Innovation Centre, Aarhus
We are looking for two new Sensory Panel Leads. One new collegue for a 1 year maternity cover and one for a 3 year project. For both positions we hope we will be able to prolong the employment or offer new challenges within Arla Foods.
Your key responsibilities will be:
- In close contact with stakeholders, guide and choose the proper test-setup to deliver the sensory results needed
- Panel training and development of panel competences within specific areas of interest
Regulatory Affairs Specialist
The RA Specialist for Radiometer is responsible for ensuring coordination of regulatory activities for a few of our Blood Gas products manufactured in California to help ensure continued compliance in all markets.
In this role, you will have the opportunity to:
- Facilitate coordination of regulatory activities between California and Denmark for design control activities and international registrations for a few of the instruments/consumables manufactured in our California site.
- Ensure compliance with EU regulations.
- Generate STED files, international submissions & assess design changes.
- Plan and execute projects for new regulatory requirements.
Senior Regulatory Specialist
The Senior Regulatory Affairs Specialist at Radiometer is responsible for collecting and generating documentation for product submissions to ensure compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world.
If you thrive in a fast-paced environment, are used to playing a critical supporting role and want to work in a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.
Project Manager - Sustaining Engineering & PMO
We are looking for an experienced Project Manager to join our PMO, Technology and Innovation. You will lead sustaining engineering projects with multidisciplinary teams of engineers and specialists.
You will apply your project management, people leadership, and technical skills to qualify and implement changes to existing products e.g., material changes or quality updates. Together with your team you create clear ambitious plans and ensure projects are delivered on time with agreed quality, scope and cost.
Regulatory Affairs Manager
The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.
This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:
- Ensure regulatory compliance to maintain market approvals
- Lead a team of skilled RA associates
- Ensure alignment with relevant stakeholders
Food Technician - Arhus
Are you passionate about turning ideas into concrete products via your hands-on technical skills?
As Food Technician you will be the prime responsible for running pilot scale trial-production of a wide range of dairy/’plant based’ products. Your work will always happen in close collaboration with product developers/food designers. To be more specific, you will:
- Perform pilot trials within a wide variety of product and technology areas
- Contribute to the preparation of the test proposal and help plan the trials
Senior Supplier Quality Engineer
This is a key role within the Global Quality function, where you will have the objective of supporting the maintenance and improvement of ConvaTec’s Global Supplier Quality program and conducting supplier audits to ensure compliance.
Key Duties & Responsibilities
- Support and lead where appropriate, supplier selection, evaluation, and approval.
- Generate appropriate key performance indicators to assess supplier.
- Drive resolution of corrective actions.
Senior International Medical Manager
Are you a Medical Doctor with an interest in clinical development of pharmaceutical drugs, medical devices and digital health?
Director of Clinical Trial Simulations (PK/PD)
Are you prepared to be a game-changer in drug development?
Clinical Data Standards Specialist
Do you want to work with standardising data in clinical trial?
Corporate Vice President (CVP) Clinical Reporting within Development
Are you a seasoned leader with experience from a large, complex, and international pharmaceutical company?
Medical Scientific Liaison Renal Acute
Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company.
Delegated QP for QA Finished Goods Manufacturing
We are looking for an experienced delegated Qualified Person (QP) to join our successful QA team supporting Finished Goods Manufacturing (FGM).
International Medical Director - Clinical Development Diabetes
Are you a Medical Doctor (MD) with a solid industry experience and curious about the opportunities at Novo Nordisk?