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Project Manager PMO - Medical Devices
We are looking for an experienced Project Manager to join our Technology and Innovation PMO organisation.
You will lead multidisciplinary teams of engineers and specialists, applying your project management, people leadership, and technical skills to develop new products, variants or upgrades.
Chemical Engineer – build pilot plants to create green ammonia
2% of the global CO2 emissions originate from ammonia production. Do you also think that is 2% too much? And do you want to be the mastermind behind the pilot plants that will let us scale up our prototype to a demonstration unit?
Then join us and get your daily dose of entrepreneurial startup spirit while enjoying flexible working hours.
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.
Produktionstekniker/Laborant - Maskiner til vandbehandling
Brænder du for produktionsteknik og laboratoriearbejde, og har du lyst til at være med til producere en ny miljørigtig generation af vandrensningsteknologi, så har denne veletablerede opstartsvirksomhed med globale ambitioner jobbet til dig.
Du kommer til at arbejde med almindeligt laboratoriearbejde og arbejde med spraydeponering samt support til stack fremstilling, men da der er tale om en meget alsidig stilling, vil du også få en del opgaver der relaterer sig til udvikling, opsætning og overvågning af eksperimenter.
(Senior) Drug Substance Specialist
We are currently seeking a (Senior) Drug Substance Specialist who is energized by collaborative and fun teamwork, excels in handling complex tasks, and enjoys continuous learning.
Your responsibilities will include late-stage drug substance development, up-scaling and process validation as well as support in the commercial phase. Effective coordination with external partners is a significant aspect of this role.
Senior QA Specialist
You will be part of our QA Business Support Team, consisting of 12 QA Specialists and Senior QA Specialists, allocated to projects including innovation projects, capacity projects and strategic QA/QC projects. We participate in projects both as quality and compliance experts to ensure compliance with the requirements for Class III Medical Devices.
We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.
Regulatory Affairs Clinical Specialist
Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.
Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.
Specialist, Regulatory Affairs (Temporary Position)
As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.
Further, your main responsibilities include to:
- Gather information and documentation for variation applications
- Update dossier sections
Scientist (maternity leave temp), cell-based immunotherapies
Are you enthusiastic about developing next generation cell-based immunotherapies that bring new hope to late-stage cancer patients?
You will help the R&D team in a 6-months temporary position as one of our coworkers is on maternity leave, and will help the team with a possibility for further extension.
We are looking for a person experienced in immune oncology or related area with documented practical experience in cell culture and flow cytometry.
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.
Principal DMPK Scientist
Currently, we are looking for a new principal DMPK scientist, who has experience in supporting discovery and development projects in characterization and selection of drug candidates.
Responsibilities
- Design, conduct, and manage in vitro, and in vivo experiments to evaluate the ADME and PK profiles as well as toxicokinetics of drug candidates both in-house and at contract research organizations
- Develop and execute assays for measuring drug concentration and metabolite identification from in vitro and in vivo experiments