...ikoniske brands indenfor konfekture deklareres og mærkes korrekt? Så er denne stilling måske noget for dig:
Velkommen til Quality & Regulatory
Den regulatoriske verden udvikler og ændrer sig konstant, og vi har brug for en ny kollega til vores regulatoriske team. I det...
...projects related to rebuilding, shutdown activities, improving Drug Substance and Drug Product production processes, and ensuring regulatory compliance.
Are you our next pioneer?
Succeeding with our vision of becoming one of the largest pure-play vaccine companies...
...hospitals and care homes to provide efficient, stress-free patient care.
We are seeking a highly motivated and detail-oriented Regulatory and Compliance Specialist to join our team in Copenhagen. This role is critical in ensuring that our AI products and services comply...
...the growing product portfolio and life cycle management activities in Novo Nordisk? Would you like to be part of shaping how we in Regulatory Affairs drive data integrations/migrations using digital tools/automation?
If you are ready to take on the challenge, we...
...Sr. Regulatory Publisher
(Global Regulatory Publishing, Regulatory Business Operations)
Lundbeck’s passion links to our purpose of restoring brain health so every person can be their best. We strive to make a real difference to patients. By developing innovative...
...Join a fast-changing environment where people do their best to get Novo Nordisk products approved across the globe. In Global Regulatory Affairs, o ur people have a unique combination of scientific insight and ability to navigate many external requirements and stakeholders...
...Do you want to play a key role in accelerating the development of our patient-focused products? Are you passionate about regulatory science and executing on regulatory strategies to bring innovative medicines to patients?
If so, we invite you to become a part...
...Regulatory Data Manager – RIMS Business Administrator
We are looking for a business administrator for our regulatory information management system (RIS). The RIS team, part of Lundbeck’s Global Regulatory Operations department, is responsible for the management...
...evt. med mulighed for deltid (min. 30 timer).
Har du interesse for og meget gerne erfaring med Regulatory Affairs – og helt optimalt med Marketing Compliance - og vil du gerne arbejde mere målrettet med Marketing Compliance, så er der måske her en udfordring til dig...
...at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.
The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for...
...flexibility, and continued compliance.
Key responsibilities of this role include:
To define and actively drive implementation of regulatory strategies from facilities point of view for product launch, capacity expansion, and other strategic projects going across the...
...have experience from either RA, CMC, QA, and/or QC – or any other relevant area? Do you possess a natural interest and flair for regulatory guidelines? Do you enjoy being part of a team where you together build and work on the timely delivery of successful submissions?...
...Are you passionate about shaping future regulatory frameworks and policies? Do you thrive in solving unique and complex problems that have a significant impact on the development of future medicines and devices? If so, we have an exciting opportunity for you to join our...
...Europe and the UK. As we continue to scale our impact, we are looking for a Senior Software Engineer with a focus on the finance and regulatory domains to join our Tech department in Copenhagen or Aarhus. For this position, you will report to Simon Stubben, our Head of...
...Are you passionate about technical writing (incl. IP) and/or regulatory submission process and the subsequent Q&A process? Do you have experience from working with API manufacturing processes and/or the regulatory field? We are looking for a new colleague to join a team...
...navigate political agendas and external stakeholders? If yes, you might be the new Data Science Policy Specialist we are looking for in Regulatory Affairs.
We are seeking an enthusiastic specialist to be at the forefront of bridging the gap between advances in data...
...Are you experienced within device regulatory affairs and are you passionate about finding new pathways for approval of combination products then this might be an interesting job for you
The role
Ascendis Pharmais a fast-growing, dynamic biopharmaceutical company...
...more people, more effectively. The external requirements to the medical device industry are increasing and we are a Global Group Regulatory Affairs team of approx. 10 persons who facilitate and actively participate in ensuring that WSA adheres to the right standards of...
...Category: Regulatory Affairs
Country/Region: DK
Location: Odense, DK, 5260 Søborg, DK, 2860 One of our employees has taken the opportunity to work at one of our production sites for the next year. We are therefore looking for a replacement until end of April 2025...
...energy sector, with hands-on experience or a keen interest in sustainable transportation, renewable energy technologies, and related regulatory frameworks.
Experience: Proven experience in content creation, journalism, or a similar field, with a strong portfolio...
...Possess hands-on experience in validation within the pharmaceutical or medical devices industry
Demonstrate in-depth knowledge with regulatory requirements for validation, including drug, combination, and device products
Showcase a keen understanding of validation...
...responsibility of the team is:
- Provide specialized HVAC support within the aseptic manufacturing environment, ensuring compliance with regulatory requirements and company standards.
- Perform routine maintenance and troubleshooting of HVAC systems to ensure optimal...
...best solution in collaboration with our stakeholders. Furthermore, you can make independent decisions and navigate in a complex regulatory environment, proactively interacting with various colleagues and teams.
About the department
DMD is a project organisation...
...Audits: Perform comprehensive audits of Danish-based clients' IT infrastructure, systems, and processes to assess compliance with regulatory requirements, industry standards, and best practices.
# Risk Assessment: Identify and analyze IT-related risks and...
...and imputation methods. You will also take part in the development of submission documents and be involved in interactions with regulatory authorities.
You will not be directly involved in the clinical trial conduct but rather oversee the project while mentoring less...
...across the organization
• Linking programme and redefining current scoped project, related to early and structured planning of regulatory submissions and approvals, to next level
• Driving and overseeing the cross organisational project programme with several individual...
...successful execution of experiments.
Analyse, interpret, and model DMPK and PK/PD data, contributing to scientific publications and regulatory submissions.
Present research findings at internal and external scientific meetings and conferences.
What they are Looking...
...counterparties, run the KYC process, perform Sanction Screenings and to advise and support the business with in-depth knowledge of regulatory requirements pertaining to KYC and Sanctions. Your responsibility areas will among others be:
Know-Your-Customer (KYC),...
...System Operations and Compliance
In our department we are responsible for operation & maintenance, development, upgrades and regulatory compliance for more than 30 laboratory IT systems used within the non-clinical and clinical research and development area. We have...
...communication and interpersonal skills
Have the ability to work collaboratively in a cross-functional environment
Have knowledge of regulatory requirements related to finance and accounting
Have the ability to build effective relationships and collaborate with a range...