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PhD scholarship in Fish Bacteriology and Prophylaxis with specific Emphasis on Bacteriophages as a Control Method – DTU Aqua
Join us on our mission to monitor and promote health of fish and shellfish, with special focus on sustainable aquaculture.
You will be working within bacteriology and microbiology with emphasis on host-pathogen interactions and disease prophylaxis in fish. The focus will be the fish pathogen Flavobacterium psychrophilum and bacteriophages as a prophylactic control measure against disease outbreaks with this important pathogen in aquaculture.
Your work will be part of externally funded research projects, among them the IFD Grand Solutions project AQUAPHAGE Towards a sustainable aquaculture: Phage-based solutions for disease prevention in rainbow aquaculture.
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.
Coordinator in Quality
Are you our new coordinator within Quality? Do you enjoy working with Planning & Forecasting, Contract Laboratory Organization (CLO) management, Reference standard & Control management - then join our Data Management team within Quality in our site in Hillerød.
You will be the point of contact for CLO´s used within Quality Control (QC) ensuring the relationship and making sure contracts are in place. Your responsibilities will include monitoring of inventory levels, providing status to management and facilitating the timely delivery of products to customers.
QA Academic CMC Development
Do you want to be part of an agile, inspiring, and competent team while restoring brain health for patients worldwide?
Then join us as our new QA Academic, ensuring product quality while collaborating with multiple stakeholders leveraging your professional and personal competencies. We offer an exciting job with a broad variety in you daily work supporting CMC deliverables from early to late phase pipeline projects.
PhD scholarship in Development of Oral Vaccines for Fish – DTU Aqua
Join us on our mission to monitor and promote health of fish and shellfish, with special focus on sustainable aquaculture.
You will be working within vaccinology and immunology with emphasis on development and testing of innovative vaccine concepts in fish along with dissection of host-pathogen interactions aiming at improving our understanding the mechanisms of protective immunity in fish. Your work will be part of externally funded research projects focusing on different strategies for mucosal vaccine delivery, among others including bioencapsulation of vaccines for oral delivery.
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.
Technical supporter within quality and documentation
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?
We are looking for a colleague to join our process support team. The team is responsible for running pilot and demonstration scale fermentations and downstream operations. These days we are implementing GMP+ in our production, and we need your experience to support this process and maintain the system afterwards. In your daily work you will support management and process in updating and reviewing process documentation, coordinating training activities, and handling deviations.
Drug Substance Production Supporter
Our vaccines make a real difference to people, and no matter your role we all contribute to protecting lives every day. In Virus Production Support team your main area of responsibility will be:
- Trouble shooting in production
- Process confirmation to ensure your processes are running according to written procedures
Specialist QA Record Management
Do you have solid experience with electronic Document Management Systems (EDMS), Data Integrity, and record-keeping policies and systems?
Our vaccines make a real difference to people, and no matter your role we all contribute to protecting lives every day. This is how your work matters:
- Act as process manager for the Record Management process
- Responsible for how our EDMS systems work
- Responsible for how our physical paper archive system works
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 QA Specialist
As a member of our professional QA team, you'll be responsible for ensuring that our release and quality systems meet regulatory and industry standards. Working alongside a team of 8 QA Specialists and 2 student workers, you'll report directly to the QA Manager.
Your responsibilities will include:
- Reviewing and approving batch documentation, raw materials, process solutions, API intermediates, and final API
- Releasing materials and APIs
Raw Material Sampler for QC Raw Materials Sample Team
You will be working in the QC Sample team, a small team that of now consist of four employees and a manager, but the team is still growing.
Your primary tasks will be but not limited to:
- Sampling and inspecting raw materials in classified areas according to specifications
- Logging samples in LIMS and documenting compliance in SAP
- Expiry setting and checking quality information from our vendors on materials received
We offer an exciting journey on a fast-growing commercial pharma site with lots of development opportunities.
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.
Tech Transfer Scientist
Do you want to play a central role in ambitious projects? Are you motivated by cross-organisational tasks? Would you like to join a fast-moving international company with state-of-the-art technologies within vaccine production?
In this position you will be responsible for the transfer of Drug Product manufacturing processes, like formulation, filling, and freeze-drying.
As a scientist you will work closely together with the colleagues in the Manufacturing Science & Technology department as well as colleagues across the organization
Regulatory Affairs Manager
Are you an experienced regulatory affairs professional who is looking for a new and exciting challenge as a next step in your career?
Your main responsibilities:
- Ensure compliance with food legislation for Denmark (mainly waters).
- Being the trusted subject matter expert within EU and local food legislation for waters/drinks.
We offer a career in a purpose driven and fast-moving international company.
Regulatory Trade Policy Specialist, Arla Foods Ingredients
We are currently expanding our team and looking for a new Regulatory Trade Policy Specialist at our office in Aarhus.
Joining 12 colleagues, you will be one of our three regulatory trade experts responsible for ensuring that we have access to our global markets and understand how different trade agreements can be beneficial for Arla Foods Ingredients.
Senior Manager, Enzyme Sensors & Liquid Chemistry (mat. cover)
In this maternity cover for 10 months you will be responsible for Enzyme Sensors and Liquid Chemistry department, ensuring the technical development, quality, and supporting delivery of enzyme sensors and liquids used in the Radiometer’s product portfolio.
You will have the opportunity to lead a growing team of nine skilled engineers and specialists, fostering a collaborative and inclusive team culture that promotes driving results, competence building, and continuous improvement.
Application Technician – Dairy & Ice-Cream
Are you passionate about developing new products and testing these in new applications? Do you have experience working in a dairy-plant or a pilot dairy plant?
You will be part of the Dairy & Ice cream team in our Application department where you will have a technical role and work side-by-side with the current application technician in the pilot plant.
We offer you a job with unique working conditions, including one extra week of holiday (7th week), health insurance etc., and the possibility of further career development.
Process Supporter – Medical devices
You will be part of the production team where you will take a central role in getting Contura products released for the market.
Your strong scientific background will contribute to maintenance and update of the product and process documentation, e.g. process validations, product stability testing reports, risk analysis evaluations, design changes etc.
Your Profile:
- Civil engineer, chemist, pharmacist, microbiologist or other relevant higher education within natural science
- Medical device industry experience preferred