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Erfaren QA-Specialist – til frigivelse af produkter
Stillingen byder på et bredt udsnit af QA-opgaver og flere kan komme til, så du får gode muligheder for at videreudvikle dine QA-kompetencer.
Opgaverne:
- Selvstændig frigivelse af PKC’s produkter og behandling af afvigelser og håndtering af ændringssager
- Sparringspartner for QA-gruppen, QC-gruppen og produktionen
Du får ansvar for og stor medbestemmelse over dine opgaver. Der er tid til fordybelse, men der er også dage, hvor det går rigtig stærkt, og opgaverne blev andre end dem, du havde planlagt og forventet.
(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.
Salling Group søger projektleder til Group Sustainability
Har du lyst til at blive en del af bæredygtighedsteamet i Danmarks største dagligvarekoncern og bidrage til at indfri Salling Groups ambitiøse klimamål?
Group Sustainability er med til at sætte den strategiske retning for Salling Groups arbejde med bæredygtighed, og vi arbejder tæt sammen med forretningen i forhold til at implementere strategien.
Regulatory Affairs Clinical Specialist
Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.
Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.
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.
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.
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
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.
Niels Brock Copenhagen Business College seeks teachers to computer science, Bachelor programme
Do you find it challenging being part of a newly started Bachelor programme in Computer Science?
Does it appeal to you to teach computer science in an international environment?
The programme contains both up-to-date subjects like AI, Big Data, and Agile Development and classic disciplines like Database design and implementation, Programming, and Data Structures and Algorithms but also development projects with both individual and group elements.