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83 jobannoncer matcher din søgning 83 jobannoncer fundet
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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) 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.
Senior Scientist, Infectious Disease Vaccine Discovery and Research
You will conduct various laboratory activities with the primary goal of producing reliable test results and optimizing lab procedures while adhering to correct procedures as well as health and safety guidelines. The role also includes documentation and reporting of results both in writing and in different forums.
You will work with dedicated colleagues in an inspiring and fast-moving environment with a collaborative and innovative spirit.
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.
SAP Master Data Specialist
Do you want to be a part of Process Support in a company with a unique impact on global healthcare?
You will be coordinating SAP production master data activities throughout the organization in order to achieve safe and predictable product implementation, maintenance, and decommissioning.
Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.
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
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.
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.
Senior Process Specialist
Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.
You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.
Process Specialist
Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.
Together with the rest of the team, you will be responsible for the daily support of our production lines. You will learn our processes in detail and gain a good overview of the documentation used in production.
Kickstart your career as a Life Science Business Consultant
Looking for the opportunity to combine your interest in life sciences with the business aspects of consulting?
Then grab this career-building chance to work with and learn from talented colleagues as you help digitalize the clinical landscape for clients across the globe.
Not only will you get to hone the skills that will make you a good consultant, but you’ll also get to see the direct impact of your work as you help pharma companies make a difference in patients’ lives
Experienced GMP Partner
Are you passionate about compliance, structure, and continuous improvements?
Manager of Safety Surveillance Early Development
Do you want to play a key role in driving the ongoing safety surveillance activities for early development projects in Novo Nordisk?
Senior International Medical Manager
Are you a Medical Doctor with an interest in clinical development of pharmaceutical drugs, medical devices and digital health?
Senior Regulatory Affairs CMC Professional
Do you have experience from either RA, CMC, QA, and/or QC – or any other relevant area?
Senior Regulatory Affairs Professional
Do you want to play a key role in accelerating the development of our patient-focused products?
Trial Manager - Clinical Development Centre Denmark
Are you passionate about management of clinical trials and would like to be part of the patient’s life change?
Trial Product Handling Professional
Do you have a desire to support processes around Trial Product Handling at the clinical sites globally which is essential for the Novo Nordisk’s clinical trials?
QC Instrument Engineer for QC Instrument Support
Are you energized by identifying and implementing automated and nimble solutions to help end-users?