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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.
Manager Virus Production
Do you want to play a central and important role in Bavarian Nordic´s manufacturing strategy by setting directions and ensuring smooth daily operation in our production facility?
Our newly established Drug Substance Facility in Kvistgaard will soon start production ramp-up, and we therefore need to strengthen our leadership. You will become responsible for the day-to-day shopfloor management of 15-20 operators.
Senior Specialist til QC hos Xellia Pharmaceuticals
Drømmer du om mere ansvar, med forskelligartede opgaver, og har du en passion for mikrobiologi? Vil du spille en central rolle i Xellias produktionen af livsvigtig antibiotika?
Som senior specialist vil du blive faglig ansvarlig for vores count release-laboratorie, som bl.a. udfører TVC- og LAL-analyser. Derudover vil du indgå i tæt samarbejde med vores sterile produktioner angående EM, hvor de nye Annex 1-krav stiller øgede krav til vores compliance, som du vil spille en vigtig rolle i.
Clinical Supply Manager
The Clinical Supply Manager will be managing outsourcing of packaging, labelling, and distribution of clinical trial supplies for all clinical trials.
You must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.
We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.
Senior Data Manager
The Senior Clinical Data Manager is responsible for leading and overseeing data management activities associated with clinical trials, ensuring data accuracy and consistency, and managing data cleaning and quality control processes.
We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.
Professional, Visual Inspection
Kunne du tænke dig at være med i et spændende eventyr hos en fabrik i rivende udvikling? Har du erfaring med GMP i lægemiddelindustrien?
Du vil blive en del af Production Support og vil være tilknyttet visuel inspektionsprocessen, hvor du vil være med til at sikre proces, procedurer, GMP og generelle forbedringer på vores proces.
Application Specialist – Beverages
Are you passionate about product development within all types of beverages from premium organic CSD's to flavored spirits?
You will work in a high-paced, collaborative and energetic environment optimizing key elements of beverage applications such as taste, stability, preservation and appearance with the goal to design the perfect balance between these elements.
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.
Medical Advisor med kommerciel tilgang
Har du lyst til at arbejde sammen med dygtige og passionerede kolleger, hvor du kan gøre en stor forskel med dine faglige kompetencer og være en vigtig drivkraft i at udvikle det faglige samarbejde med vores kunder?
Din primære opgave er at rådgive omkring vores produkter i den primære og sekundære sektor. Herunder at opbygge et tæt netværk af relevante health care professionals.
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.
Senior Medical Writer
Do you want to work in a global context and according to the highest standards of current practice to provide new products to patients with unmet medical needs?
As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.
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.
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.
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.
Technician, EMA Solids Support Team
Welcome to Solid Support Team 13 skilled process engineers and technicians responsible for quality, introducing new products, throughput, and optimizing the products.
In this role you’ll make an impact by:
- Responsible technician for the MG-coating line, ensuring smooth and efficient coating processes for granulating with MnTACN
- Coordinate the steering system changes, bridging the gap between process engineers, technicians, and programmers to optimize operational efficiency.
Driftsleder/Procesleder til industribageri
Er du klar til næste skridt i din karriere inden for produktion?
På bageriet i Avedøre søger vi en procesleder, der vil være med til at sikre en stabil produktion. Du får ansvaret for driften i bageriet. Personalet dækker ca. 15 faste medarbejdere.
Du går forrest, evner at arbejde på tværs og skabe opbakning hele vejen rundt. Og dit fokus på udvikling af processer skaber succes i stillingen.
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
GMP-Supporter - Danmark Protein, Videbaek
Som GMP-supporter med fokus på forbedringskultur, leder du konstant efter måder at gøre vores produktionsmiljø bedre på. Dette gælder for sikkerhed og kvalitet.
Dine opgaver vil svinge mellem at være driftsorienterede, såsom GMP-runderinger til forbedringsaktiviteter og være projektorienterede, hvor du selv driver forbedringsprojekter, støtter og udfordrer vores teams og medarbejdere på deres rejse mod en forbedringskultur.
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.