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32 jobannoncer matcher din søgning 32 jobannoncer fundet
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(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.
Drug Substance CIP Process Supporter
Are you passionate about pharmaceutical CIP? Do you know processes and optimizing production?
As a CIP Process Supporter (Cleaning In Place), you will have a cross-functional role as a link between production, support teams, and technical support.
Your primary focus will involve optimizing our vaccine production and ensuring robust operation in line with CIP requirements and regulations. Additionally, you will play a vital role in daily troubleshooting, collaborating across diverse professional groups to ensure a streamlined production process.
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.
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.
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
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.
Ruminant Nutritionist – Calf and Lamb Milk Formulations
This is an great opportunity to join our international team that continues to invest in the Ruminant offering looking at way to innovate and enhance our formulations, and additives that support the needs of young animals with some other responsibilities such as:
- Supporting R&D activities, including feed material and product evaluations, trials, and commercial interpretation and communication.
- Develop technical ideas to add value to product sales and marketing.
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.
Project Coordinator
Do you have experience managing projects anchored to a GMP facility? Are you eager to contribute to the development of a newly established project team in a production environment?
As a Project Coordinator, you will participate in the successful planning and completion of projects related to the Drug Substance Manufacturing Processes. You will coordinate and follow up on a number of tracks that links to various projects.
Senior Scientist - Enzyme Development - Animal Nutrition and Health
Would you like to be part of a world leading international team developing groundbreaking enzyme solutions for Animal Nutrition and Health?
You will join dedicated project teams and work with leading scientists from around the world on new enzyme-based products for major global companies. And you can apply world class industrial bioscience competencies to generate new sustainable solutions for Animal Nutrition and Health.
Engineering Project Manager
Har du en passion for at drive teknologisk udvikling og bruge dine kompetencer i den grønne industrielle omstilling?
Den succesfulde kandidat vil have en ledende rolle i ALGIECEL's full-scale demonstrationsprojekt, der transformerer CO2-emissionerne på Novonesis' faciliteter i Kalundborg til bæredygtige algebaserede produkter gennem en yderst effektiv og kompakt fotobioreaktor.
Tiden for forandring er nu, og dette er din chance for at blive en del af vores højt motiverede team!
Principal Clinical Safety Advisor for Pharmacovigilance & Safety
Would you like to utilize your competencies within clinical trials broadly and influence projects?
Environmental Monitoring Supporter
Do you have an interest in daily operations activities across a manufacturing unit producing lifesaving medicine?
Quality and Training Coordinator
Are you passionate about quality management and dedicated to fostering a culture of continuous improvement?
Raw Material Scientist
Are you prepared to lead the way in the dynamic field of materials for GMP production?
Formulation Professional
Do you have in depth experience within formulation of drug product, and a service mindset to support global manufacturing of Injectable Finished Product?
Product Stability Scientist
Are you passionate about working with solid dose products and other emerging technologies?
Associate Director in RA CMC & Devices
Would you like to be part of an area where we bring treatments to patients?
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...