17 jobannoncer matcher din søgning 17 jobannoncer fundet

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.

Creative Assistant

Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?

Your Focus will be:

• Always following correct compounding procedures
• Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
• Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.

Laborant/Lab Technician

Do you want to help our customers with developing their future or existing products? The Innovation Center in Silkeborg, are conducting a lot of different tests from customer all around the world, within food & beverage.

The laboratory technician will be responsible for the laboratory in the innovation center in Silkeborg, providing the needed analysis for our customers during the different trials we conduct in the test center, be responsible for keeping the laboratory fully equipped, take care of the customers questions, and to ensure that the laboratory always stays presentable.

Technical Specialist, Product Quality, Nourish (Maternity cover, 12 months)

Are you an enthusiastic, motivated and detail-oriented professional with a desire to work in a team of colleagues with great technical competencies within production, regulation and processes?

Your core responsibilities:

• Handling deviations for products manufactured at our factories.
• Handling of product quality related complaints.
• Coordinate and implement customer-specific requirements. Maintenance of master data in various IT systems, including SAP.

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.

QEHS Manager

Unique opportunity to join an innovative biotech company with a proven and sustainable technology on the edge of global expansion.

Do you want to help develop the protein of the future, which will make it possible to feed the world's growing population without damaging our ecosystems?

You will be leading a small team responsible for managing and coordinating all QEHS activities, including certifications, audits, and training. You will ensure that operations are conducted in a safe and efficient manner and in conformance with safety regulations.

Senior Test Engineer

Join GE HealthCare to help perform transducer integration on our next-generation ultrasound scanners and further develop our test tools and laboratories.

As our new Senior Test Engineer, your typical tasks will include measurements of sound pressure, acoustic power, thermal characteristics, image performance and other transducer properties.

You will take part in hands-on work while also playing a key role in maintaining and further developing our transducer integration processes and two laboratories.

Laborant/Senior Laborant

I jobbet som Laborant/Senior Laborant i Translational Pharmacology vil du være ansvarlig for planlægning, koordinering og gennemførelse af in vivo / ex vivo farmakologiske eksperimenter som bidrag til vores prækliniske forskningsprojekter.

Ansvarsområderne omfatter bl.a.:

• Gennemførelse af in vivo-undersøgelser af høj kvalitet i gnavere, herunder bidrag til protokoller, planlægning, udførelse og dokumentation.
• Udførelse af grundlæggende kirurgi hos gnavere, herunder anæstesi og analgesi.
• Prøvetagning og håndtering af blod- og vævsprøver af høj kvalitet.

Analytical Chemist – 12 months position

We seek a highly motivated ANALYTICAL CHEMISTRY scientist, engineer, or technician for our research laboratory in Copenhagen.

The position will give intellectual challenge and rich possibilities to develop your skill sets as well as being part of commercially and scientifically exciting projects.

You will contribute to the development and maintenance of River Stone’s analysis platform, method development as well as routine sample analysis. You will be part of an enthusiastic and strong analytical chemistry team.

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

Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.

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 QA Specialist

The Senior QA Specialist for Radiometer is responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms. This is done by cooperating, supporting, facilitating, training, and communicating towards the best results with partners in R&D.

This position is part of the QA Design Control department, hybrid based and located in Brønshøj. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.

QA Specialist

You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms.

You will have the opportunity to:

• Provide Design Control guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment.
• Represent Quality Assurance in design and development projects and in cross-functional teams supporting new product development.