5 job matcher din søgning
Arla Foods, Viby J.
Are you ready to use your expert knowledge of how nutritional components affects the human physiology and biochemistry?
As Nutrition Scientist in the commercial business unit, “Health and Performance”, your work will focus on collecting, communicating and creating scientific documentation for the health effects of our ingredients for use in medical nutrition products. It will be your responsibility to manage a series of clinical trials within this area, and you will be overall accountable for securing the nutrition science evidence base supporting our ingredients.
Moreover, you are an essential part of the development of sales and marketing material and provide input to the development of new ingredients. As such, you also contribute to fuelling our ingredient pipeline with innovative ideas and a basis of valid knowledge for the further development of new products.
Arla Foods, Viby J.
Can you lead and inspire a knowledgeable team? And would you like to influence the strategy of a global leader in industrial food ingredients?
In collaboration with Sales, you become globally responsible for driving and implementing our value add product and sales strategy, just as you set the focus for our documentation strategy in collaboration with our team of nutrition scientists. In more detail, you:
- Act as an inspiring, coaching and motivating manager who actively support the strategy execution for our products, market segments and business area
- Help your team utilise their nutritional and technical knowledge surrounding our products to facilitate the strategic value-added sales
- Make sure your team can support all geographies and customers and travel 30-40 days a year to visit trade shows and customers yourself
Kevin Murphy Europe A/S, Copenhagen
Reporting to the Global Director of Procurement, the Global Regulatory Affairs Manager will be responsible for leading activities of the Regulatory Affairs Department with an emphasis on global regulatory strategy and the preparation, review and submission of documents to any regulatory authorities at a global level.
Oversees the regulation process for products requiring governmental approval, including filing necessary applications and handling all government interactions in the geographical areas where KEVIN.MURPHY Group products are marketed. Coordinates inspection of the organization and contract facilities and develops procedures to ensure regulatory compliance. Requires a Master's degree in the area of specialty.
Ambu A/S, Ballerup
Are you looking for a job with a high degree of influence and a varied working day? Do you want to be part of developing professional and safe medical devices? Moreover, do you have a high energy level?
As part of the Corporate Clinical Research & Biosafety department, you will work closely with Global Innovation teams, as well as Marketing teams, to develop medical devices.
In the job as Clinical Research Specialist/Medical Writer, your main responsibility will be to participate in product development projects, and to provide clinical and medical writing input to ensure safe and efficient devices.
You will be involved in all clinical and medical writing aspects of product development, including to:
- Prepare clinical documentation to support product approval
- Plan, coordinate, execute, and report pre-clinical activities, and clinical investigations
Radiometer Medical ApS, Brønshøj
6 samples are tested using Radiometer’s Medical Device analyzers every second. That’s 360 a minute, 21,600 an hour, 518,400 a day. If you love numbers like we do, imagine the data and feedback we get regarding the quality of our products. These numbers and the analysis of our product performance can be an integral part of your next job.
So get ready for a new challenge and bring your excel data crunching skills, your technological curiosity and the passion for presenting numbers to important stakeholders among Radiometer’s dedicated employees and managers.
Your new position is key for trending on complaints and unplanned service work orders, which in turn provides key input to which counter measures needs to be taken. It is also important to provide the data needed for follow up on quality parameters (showing up in complaints) as well as providing input for management reviews.