96 jobannoncer matcher din søgning 96 jobannoncer fundet

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.

Product Sustainability Specialist

Vi søger en kollega, der sammen med afdelingens øvrige specialister kan sikre, at Flüggers produkter er i overensstemmelse med lovgivningen, samt opfylder kravene til de forskellige frivillige ordninger indenfor bæredygtighed.

Du vil få en spændende og afvekslende hverdag, hvor du vil være ansvarlig for planlægning og udførelse af egne opgaver. Opgaverne er mangeartede og der er stor mulighed for personlig udvikling.

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

Application Specialist – Beverages

Are you passionate about product development within all types of beverages from premium organic CSD's to flavored spirits?

You will work in a high-paced, collaborative and energetic environment optimizing key elements of beverage applications such as taste, stability, preservation and appearance with the goal to design the perfect balance between these elements.

Senior Manager Public Affairs & Communications

Are you prepared to leverage your comprehensive communication skills to contribute to Danish Crown's public affairs strategy and ambitious reputation agenda as a food company for the future?

If you want to be a part of making real change in the food industry, Danish Crown is the team to join – the task ahead is clear - we want to be a leading player in transforming the future of food production in Denmark and beyond. Together with our team of top-class communication professionals you will be a vital part of supporting this change.

Senior Medical Writer

Do you want to work in a global context and according to the highest standards of current practice to provide new products to patients with unmet medical needs?

As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.

Sales Trader

We are looking for a Sales Trader who will play a vital role in ensuring BioCirc’s ambitious growth plans.

The successful candidate will together with the Portfolio Manager be responsible for the short-term sale of Certificates, optimizing the portfolio, gather market intelligence, and ensuring value added through the whole supply chain of biomethane production, but also new renewable products stemming from our energy clusters.

Student Assistants for NBCD A/S within Clinical Operations

Do you dream of working with pharma and research? Are you curious, service-minded, and envision yourself thriving in a dynamic research environment with varied tasks?

Then come join us as a student assistant and become part of a company, that operate at the forefront of international drug development research, where you'll have the opportunity to broaden your skillset, shape your own day and contribute to various projects.

Technical Specialist, Product Quality, Nourish (Maternity cover, 12 months)

Are you an enthusiastic, motivated and detail-oriented professional with a desire to work in a team of colleagues with great technical competencies within production, regulation and processes?

Your core responsibilities:

• Handling deviations for products manufactured at our factories.
• Handling of product quality related complaints.
• Coordinate and implement customer-specific requirements. Maintenance of master data in various IT systems, including SAP.

Regulatory Affairs Specialist

The RA Specialist for Radiometer is responsible for ensuring coordination of regulatory activities for a few of our Blood Gas products manufactured in California to help ensure continued compliance in all markets.

In this role, you will have the opportunity to:

• Facilitate coordination of regulatory activities between California and Denmark for design control activities and international registrations for a few of the instruments/consumables manufactured in our California site.
• Ensure compliance with EU regulations.
• Generate STED files, international submissions & assess design changes.
• Plan and execute projects for new regulatory requirements.

Senior Regulatory Specialist

The Senior Regulatory Affairs Specialist at Radiometer is responsible for collecting and generating documentation for product submissions to ensure compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world.

If you thrive in a fast-paced environment, are used to playing a critical supporting role and want to work in a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.

QEHS Manager

Unique opportunity to join an innovative biotech company with a proven and sustainable technology on the edge of global expansion.

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?

You will be leading a small team responsible for managing and coordinating all QEHS activities, including certifications, audits, and training. You will ensure that operations are conducted in a safe and efficient manner and in conformance with safety regulations.

Regulatory Affairs & QA Lead

Har du lyst til at blive en del af en spændende arbejdsplads, som opererer globalt med nogle af markedets bedste produkter?

Som vores Regulatory Affairs & QA Lead bliver du en del af et velfungerende team med 5 engagerede kolleger, der hver dag arbejder målrettet og brænder for deres arbejde.

Der kan være mange indgangsvinkler til jobbet men du skal have erfaring med medicinsk udstyr, være omhyggelig, energisk og brænde for det regulatoriske arbejde.

Senior Social Media Advisor

Join us in this role where you’ll help build our brand, grow our communities on our global social media channels, and launch new initiatives that take us to the next level.

Using your international experience, you’ll create content that captivates and inspires our communities across LinkedIn, X, Facebook, and Instagram, and use your knowledge on how to handle community management in a global environment.

Legal Counsel med interesse i Forbruger- og Markedsføringsret

Kunne du tænkte dig at arbejde i en intern juridisk funktion i en global virksomhed, hvor du har direkte indflydelse på forretningen?

I rollen som Legal Counsel indtræder du i en specialistrolle, hvor dit primære ansvarsområde ligger indenfor håndtering af juridiske problemstillinger med fokus på Forbruger- og Markedsføringsret. Derudover vil en stor del af dit arbejde bestå af at vurdere og formidle den regulatoriske, juridiske og omdømmemæssige risiko, der er forbundet med de forskellige løsninger, som du, sammen med forretningen, finder frem til.

Legal Counsel med interesse for Privacy og GDPR

Kunne du tænke dig at arbejde i en intern juridisk funktion i en global virksomhed, hvor du har direkte indflydelse på forretningen?

I rollen som Legal Counsel indtræder du i en specialistrolle, hvor dit primære ansvarsområde ligger indenfor håndtering af juridiske kontrakter med fokus på Privacy og GDPR. Derudover vil en stor del af dit arbejde bestå af at vurdere og formidle den regulatoriske, juridiske og omdømmemæssige risiko, der er forbundet med de forskellige løsninger, som du, sammen med forretningen, finder frem til.

Regulatory Affairs Manager

The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.

This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:

• Ensure regulatory compliance to maintain market approvals
• Lead a team of skilled RA associates
• Ensure alignment with relevant stakeholders

Praktikanter til Forbrugerrådet Tænk

Har du lyst til at komme i praktik i en professionel ngo og bidrage til vores arbejde til gavn for de danske forbrugere, mens du udvikler dig som studerende? Forbrugerrådet Tænk har startet et nyt praktikantprogram op, og vi søger 6 studerende til et fælles praktikforløb i efterårssemestret 2024.

Forbrugerrådet Tænk søger 6 praktikanter med forskellige faglige profiler, som har lyst til i en periode at supplere studierne med praktisk erfaring fra en spændende arbejdsplads med ca. 110 engagerede kollegaer med mange forskellige fagligheder.

We are looking for a dedicated and engaged PR and Content Manager

As one of the largest tech consulting companies in the Nordics, we're ambitious about our future, aiming to triple in size over the next 5 years. To achieve this goal, we recognize the importance of investing in building a robust brand.

As our PR and Content Manager, you'll be an integral part of a team dedicated to strengthening our brand. Your responsibilities will include crafting timely press releases, articles, references, and content that supports our marketing and communication strategies.

Technical Writer to GE HealthCare Denmark

Join GE HealthCare to help develop high quality instructions for use for our ultrasound scanners, transducers, and reprocessing methods in compliance with rules and legislation in various countries. This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

Our Technical Documentation team consists of six dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities. Our Technical Writers develop and maintain the user documentation for our high-performance equipment.