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Clinical Project Manager
Do you want impact, freedom to perform, global perspective and super colleagues?
As experienced Clinical Project Manager, you naturally know that your success is built on your ability to generate high quality data at high pace and within agreed budgets – without jeopardizing the good relationship to the people and partners involved. Another vital part of your road to success is your ability to think outside the box and handle (unforeseen) challenges on the way.
Senior LIMS Specialist for Global QC Development
In this role you’ll make an impact by working as a Senior LIMS Specialist in our team, where you will take part in management of projects for LIMS changes across QC laboratories and other stakeholders including implementation, documentation and communication.
Future projects could be introducing and validating LIMS solutions on new equipment or technologies, new LIMS functionalities, improving and aligning existing processes.
Test & Reliability Engineer - Sustaining Engineering, Medical Devices
Do you have a keen eye for Physical Testing, Product Quality, Reliability, Validation, and Documentation? Are you looking for an opportunity to merge your passion with our expertise in the Test and Verification of Infusion Care Medical Devices, for the treatment of chronic diseases such as Diabetes and Parkinson’s Disease?
As a Test Engineer, you will be involved in developing and working with a diversity of physical test methods. Planning and coordinating tests in our laboratory in Osted near Roskilde, and partners within Global Convatec and external. Most of your time, you will be part of a project team in SEG.
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.
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.
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.
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.
Project Manager - Sustaining Engineering & PMO
We are looking for an experienced Project Manager to join our PMO, Technology and Innovation. You will lead sustaining engineering projects with multidisciplinary teams of engineers and specialists.
You will apply your project management, people leadership, and technical skills to qualify and implement changes to existing products e.g., material changes or quality updates. Together with your team you create clear ambitious plans and ensure projects are delivered on time with agreed quality, scope and cost.
Senior Supplier Quality Engineer
This is a key role within the Global Quality function, where you will have the objective of supporting the maintenance and improvement of ConvaTec’s Global Supplier Quality program and conducting supplier audits to ensure compliance.
Key Duties & Responsibilities
- Support and lead where appropriate, supplier selection, evaluation, and approval.
- Generate appropriate key performance indicators to assess supplier.
- Drive resolution of corrective actions.
Kvalitetskoordinator til DAVA Foods - bliv en del af den plantebaserede udvikling!
Til nyoprettet stilling søges en engageret kvalitetskoordinator, som har lyst til at være med på en spændende rejse inden for plantebaserede fødevarer.
Dine primære ansvarsområder vil som udgangspunkt være at:
- Udvikle og implementere procedurer for kvalitetskontrol
- Gennemføre regelmæssige inspektioner og audits
- Identificere og adressere potentielle kvalitetsudfordringer
Bliv en del af en dynamisk organisation, hvor de ikke bare følger med udviklingen, men er med til at skabe den!
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.
Associate Manager, Cultivation Pilot Plants
Are you a strong people leader motivated by building the right team and making it thrive and perform?
Senior Regulatory Affairs Professional
Do you want to play a key role in accelerating the development of our patient-focused products?
QC Instrument Engineer for QC Instrument Support
Are you energized by identifying and implementing automated and nimble solutions to help end-users?
Principal Clinical Safety Advisor for Pharmacovigilance & Safety
Would you like to utilize your competencies within clinical trials broadly and influence projects?
Regulatory Policy Professional
Join a fast-changing environment where people do their best to get Novo Nordisk products approved across the globe.
Equipment responsible in API purification pilot facility
Would you like to help us secure the operations of our pilot plants within a growing portfolio of pharmaceutical products?
Senior Professional, Aseptic Process Drug Product MSAT
Do you have a passion for production and enjoy working with many stakeholders both internally and externally?
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...
International Medical Director - Clinical Development Diabetes
Are you a Medical Doctor (MD) with a solid industry experience and curious about the opportunities at Novo Nordisk?