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Biocompatibility Specialist
We are looking for a Biocompatibility Specialist to join the Reprocessing and Biocompatibility team for a 12-month project position.
This is a great opportunity if you would like to gain experience with biocompatibility for advanced reusable medical devices, as you will be part of a cross-functional effort on documenting the safety and performance through the lifetime of our ultrasound scanners, transducers, and accessories.
QA Specialist
We are seeking a competent new colleague to join our QA team in a dynamic and growing company.
You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.
Training Partner
Are you passionate about designing high impact training to improve ways of working?
The role will focus on re-designing the training related to onboarding our professionals working directly with our operation, our Operators, and our Laboratory Technicians.
You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words.
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.
Health, Safety and Environment (HSE) Manager
Are you a seasoned Health & Safety professional seeking an opportunity to thrive in a supportive and dynamic environment?
We have an exciting opportunity to recruit a Health & Safety Manager, you will play a crucial role in maintaining and enhancing the safety standards at our facility. Your responsibilities will include designing training programs, conducting risk assessments, identifying, and controlling hazards.
Senior Engineer Device Manufacturing
Are you passionate about cutting-edge medical technology? Do you thrive in a collaborative environment where innovation drives patient care?
Amgen, a global biotechnology leader, is expanding its device development capabilities in Denmark and is seeking a talented Senior Engineer to join our Device Engineering group.
Senior Process Specialist
Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.
You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.
Senior Technical Writer - Regulatory (CMC)
You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.
Stepping into an informal and collaborative environment, you will have close interfaces with many different disciplines, including Global Pharmaceutical R&D, manufacturing sites, Product Supply, Quality Assurance, Ferring affiliates, and development sites around the world.
MS&T Program Manager
We are looking for an experienced professional from the pharmaceutical industry, who can effectively manage project plans across multiple entities and lead cross-functional processes within our own sites and supply chain.
As a MS&T Program Manager, you will be responsible for managing the projects, maintaining project databases, as well as ensuring effective communication and timely achievement of milestones.
Manufacturing Science & Technology (MS&T) Technical Transfer Project Manager (Sr Specialist)
Join Orifarm and take charge of building strong business relationships with a key portfolio of our suppliers!
As a MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to Supplier Relationship Management functions, and manufacturing sites comprising support, technological transfers between CMOs and own manufacturing sites, analytical method development and validation, external product development at CDMOs and driving continuous technological improvement and innovation.
External Lecturer – “Public Health Emergencies and Health-Crisis Management” – DIS Stockholm
DIS Stockholm is currently hiring one external faculty to co-teach the elective course Public Health Emergencies and Health-Crisis Management to highly motivated undergraduate students from North American universities who are spending a semester studying in Stockholm.
Work in an international, informal and enthusiastic environment with an emphasis on cross-cultural understanding, teamwork, innovation, and adaptability.
PhD scholarship in Fish Bacteriology and Prophylaxis with specific Emphasis on Bacteriophages as a Control Method – DTU Aqua
Join us on our mission to monitor and promote health of fish and shellfish, with special focus on sustainable aquaculture.
You will be working within bacteriology and microbiology with emphasis on host-pathogen interactions and disease prophylaxis in fish. The focus will be the fish pathogen Flavobacterium psychrophilum and bacteriophages as a prophylactic control measure against disease outbreaks with this important pathogen in aquaculture.
Your work will be part of externally funded research projects, among them the IFD Grand Solutions project AQUAPHAGE Towards a sustainable aquaculture: Phage-based solutions for disease prevention in rainbow aquaculture.
Upstream Support Specialist
Would you like be responsible for providing technical assistance within process design and process documentation?
GCP Advisor Specialist
Do you dream of using your GCP knowledge, clinical research experience and perhaps GCP audit experience and last but not least your quality...
Health & Safety Associate Manager
As our HS Associate Manager & Partner, you will lead a team focused on driving and strengthening strategies for HS projects, maintaining the...
Associate Global HEOR Director
Do you want to shape HEOR strategies to change the future access paradigm of Obesity products?
Manager in R&D Quality
Are you looking for a dynamic and challenging management role within Clinical Compliance in R&D Quality, where you can use your skills...
Senior GCP Advisor Specialist
Looking for a dynamic and challenging role within clinical process management?
Senior QA Professional with CMO expertise
Do you want to use your strong quality mind-set and great interpersonal skills to make a difference within QA?
Technical Officer (CBRN), Copenhagen, Denmark
The mission of the WHO Health Emergencies Programme (The Programme) is to help countries, and to coordinate international action, to...