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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.
Safety Medical Writer in Global Safety, (1-year parental leave cover)
Are you interested in working in drug safety and pharmacovigilance and helping to ensure the safe and effective use of medicines? Would you like to join a Safety Medical Writing team responsible for preparing medical documents for all Ferring products to ensure patient safety?
Our team is a dynamic group of six talented individuals with diverse experiences and skills. Collectively, we possess expertise in medical communication and writing. We strive for simplicity and efficiency in our processes and collaboration with stakeholders across the global Ferring organisation.
PhD scholarships in single-cell multi-omics - DTU Biosustain
The Novo Nordisk Foundation for Biosustainability (DTU Biosustain) at the Technical University of Denmark is seeking highly motivated PhD candidates with an interest in deep learning and bioinformatics approaches for cutting-edge single-cell technologies with applications in complex diseases.
If your areas of interest and competence are genomic big data science and machine learning/deep leaning framework development, and you are looking to gain experience while working on projects that will make an impact on the world, this is your chance.
Senior Technician for LIMS
Do you want to play a key role in QC?
We are looking for a skilled Senior Technician with LIMS Superuser/Static Builder skills to be part of our dedicated LIMS team of 5 dedicated employees.
Your primary tasks will be to:
- Build methods in SampleManager LIMS as well as continuous updating and optimization of existing data
- Ensure improvements and optimizations by working with systematic problem-solving according to the LEAN principles
You will be part of a global and fully integrated vaccine company committed to improving and saving lives through innovative vaccines.
Manager
Are you ready to take the lead and guide a team of competent project managers and talented specialists to new heights of success?
We are seeking a passionate people Manager to join our dynamic project and process team for this new role in Drug Product technical support at our manufacturing site in Kvistgård. You will report to the Director of Drug Product Production Support and have seven/eight direct reports.
Senior Technician
The department of Translational DMPK is currently looking for a dedicated Senior or Research Technician, who wants to be part of a developing team focused on drug metabolism and pharmacokinetics (DMPK) in early drug discovery projects.
You will support our drug research projects by delivering quantitative bioanalysis data from in vivo pharmacokinetic screening studies or pharmacological in vivo experiments of potential new drug candidates using Liquid Chromatography-Mass Spectrometry (LC-MS) techniques.
Quality Engineer Manufacturing
Are you ready to drive excellence in medical device quality at the forefront of active imaging technology?
Step into a role at BK Medical where your expertise in quality engineering directly shapes the future of surgical care. If making a tangible difference in healthcare motivates you, this role is your gateway to a fulfilling career in medical technology innovation.
Category Manager in Raw Materials Procurement
The department you will join is globally responsible for securing the raw materials for our existing productions in Denmark and USA as well as our upcoming productions related to our carbon emission reduction technologies.
You will:
- Drive category planning, management and sourcing strategies
- Have responsibility for supplier segmentation and global supply base within own categories
- Drive and negotiate strategic and partnership agreements within own categories
Sr. Project Lead, DSM expansions Go-Live
Are you seeking a new and exciting challenge in the Biopharmaceutical Industry?
Your primary tasks will entail but not be limited to driving the successful execution of project deliverables, facilitating workshops, and drive the realization of project track.
Join us and discover a community that thrives on diversity and never scares away from a complex challenge. At FDB, you determine what’s possible.
Senior R&D Scientist - Functional Ingredients
IFF is seeking a highly motivated Senior R&D Scientist to join our global Functional Ingredients R&D team to support our Nourish Division. The position requires an experienced scientist with proven track record of independently conceptualizing present and future market needs for functional food & beverage ingredients.
Key focus will be to translate market needs into technical solutions through scientific research disciplines and early stages of product discoveries across technologies and strategic focus areas such as fermented flavors.
Business Development Manager, Sustainability, Arla - Aarhus
As our new Business Development Manager, you will play a central role in executing Arla Food’s strategic priorities and ensuring we reach our ambitions.
You will be supporting the leadership team of the Agriculture, Sustainability and Communications function in delivering on their business plan and people development agenda.
You will be involved in one or more projects and your responsibilities will include driving and delivering strategic projects including managing time, scope and quality of project delivery.
Senior Manager Quality Control
Are you a highly skilled and experienced Quality Control professional in the food, beverage, or pharmaceutical industry?
As a key member of our leadership team, you will have the opportunity to shape our quality control processes and drive continuous improvement initiatives.
Join us and be a part of a company that is committed to delivering excellence in every aspect of our work.
Regulatory Affairs and ESG Specialist
As the Regulatory Affairs and ESG Specialist, you will play a key role in ensuring compliance with regulatory requirements while driving our Environmental, Social, and Governance (ESG) initiatives.
This position offers an exciting opportunity to contribute to both regulatory compliance and sustainability efforts within our organization.
We offer a challenging and rewarding opportunity to make a meaningful impact on regulatory compliance and sustainability at a global company.
(Senior) Director, Biotherapeutic Screening
Would you like to lead a department deeply involved in building our early research portfolio of monoclonal antibodies and other biotherapeutic modalities?
You can look forward to working at our state-of-the-art International PharmaScience Center (IPC) in Copenhagen, where we have invested in the newest laboratory technology, including laboratory automation, high-content imaging, and advanced flow cytometers.
Project Manager for Customer Projects, Human Health Biosolutions
As a member of the Customer Projects team you will get the opportunity to run projects related to customers request for changes or new products of dietary supplements.
Your main responsibility is to manage and coordinate customer projects from scoping to production of the first batch.
Tasks include:
- Running project meetings with key stakeholders within Novonesis and participate in customers project meetings
- Creating and managing timelines for implementation, production & delivery
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.
Medical Device & QA-specialist
Brænder du for at gøre en forskel med din QA-ekspertise for vores kunder?
Som erfaren QA-konsulent vil du bruge det meste af din tid hos vores kunder. Vi har allerede en bred vifte af kunder, vi har arbejdet med igennem mange år og der kommer kontinuerligt nye til. Vores kunder fremstiller mange forskellige typer Devices og har brug for vores hjælp og ekspertise til at løse stort set alt inden for QA/RA.
Vi tilbyder dig et fleksibelt og varieret arbejde med de mest spændende virksomheder i branchen. Det giver dig mulighed for selv at planlægge og styre dine opgaver.
Clinical Trial & Senior Clinical Trial Managers
In Zealand Pharma we are looking for several Clinical trial Managers/Senior Clinical Trial Managers to join our clinical trial teams as we pursue new and exciting therapeutic areas and optimized ways of working.
In your role as a Clinical Trial Manager, you will play a crucial role in facilitating effective collaboration among essential stakeholders involved in the execution of clinical trials. This includes close collaboration with a Clinical Research Organization (CROs) and internal stakeholders to ensure successful start-up, conduct, and closure of clinical trials.
Pet Food Senior Scientist
This role is a scientist who is going to work on petfood science (cats and dogs). The person will build in vitro lab models, which reflect the functionality in the animal.
Initially the work will be focused on existing IFF ingredients in particular enzymes but also betaine, probiotics, postbiotics, prebiotics, and phytogenic. It will also be an important task to read literature, including patent literature to identify new opportunities for application of IFF ingredients into the petfood industry, but also to help build mode of action understanding.
Senior Compliance Partner, Manufacturing
In this role, the SCP will report directly to the Director of Manufacturing and serve as a trusted partner in all GMP, quality and compliance related issues for all departments in Manufacturing.
The SCP will play a pivotal role in raising the bar for the overall quality level and ensuring a high level of compliance. In this role, you will work together with many different internal stakeholders across the site, and you will have the opportunity to influence the business and make a significant impact in the Manufacturing area.