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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.
Topsoe Operations, Technical Service Team, Service Engineer
Your primary duties will encompass routine/scheduled and unscheduled maintenance and repairs, intended at preserving our equipment and machinery in their best condition, to deliver performance guarantees and turnkey solutions with end-to-end support and onsite availability to our customers.
You will play a pivotal role in guaranteeing the optimal operation and peak performance of our equipment and technologies installed at the customer Plant facilities globally.
ESG Reporting Controller
We need you to contribute to the development of the ESG reporting and controlling processes and setup – amongst others – building a robust reporting processes procedures for collecting, validating, and controlling of ESG data, as well as preparing consolidated data and reporting.
In your daily life you will navigate in new regulatory requirements and stay updated on subsequent amendments. You will be working with external auditors and engage in close dialogues with our Corporate Communications & Sustainability team as well to other internal stakeholders.
HSE Specialist
As an HSE Specialist, you will have the opportunity to develop and implement safety policies and procedures, conduct training sessions, and ensure compliance with local, state, and federal regulations.
In joining our team, you'll have the opportunity to make a significant impact, ensuring the safety and well-being of our workforce while contributing to our continued success at Duferco Danish Steel.
Technical Drawing Engineer
Would you like to play a critical role in implementing, overseeing and management of key deliverables, and manage the repository of approved technical and regulatory drawing at Bavarian Nordic?
You will establish corporate drawing standards, manage drafting updates carried out by 3rd parties, and oversee the administration of drawing management using multiple software systems.
Software Developer for commissioning of pharma projects (C#/.NET)
Do you want to play a key role in delivering software solutions for advanced production machines?
As software developer at CIM, you will implement solutions that makes existing machines more intelligent and thereby improves performance and adds functionality leading to better patient safety and a better overall better performance.
You are the expert on what makes you happy and efficient. So, whether that entails a 4-day work week or working in the evening or from home that is simply how you will be working.
Vision Engineer – ensure the quality of pharmaceutical drugs and devices
Do you want to play a key role in delivering vision inspection solutions for advanced production machines?
As Vision Engineer, you will implement inspection solutions that improve patient safety by ensuring the quality of pharmaceutical products and devices.
You are the expert on what makes you happy and efficient. So, whether that entails a 4-day work week or working in the evening or from home that is simply how you will be working.
Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)
At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.
The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.
You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.
Student worker with attention to documentation detail for Global Business Support
Join us as our new Student worker in Global Business Support, Human Health Biosolutions
You will have the chance to be part of an ambitious and dedicated team where team spirit, high quality, attention to detail and a service-oriented mind-set is key.
You’ll make an impact by:
- Your highly valued input will make a significant difference for your team and thereby sales, customers, and consumers – evidently improving human health and wellbeing – every day.
- You will prepare and create our standard product documentation package related to new product implementations and changes.
Security Operations Specialist (SecOps) for some of the most critical IT infrastructure in Denmark
As our new Security Operations Specialist, you will have a wide range of responsibilities in operational security and security incident management.
Among other things, your work tasks include:
- collecting and analysing logs from our available sources (SIEM, networks and other applications)
- setting up alarms and ensuring a correct flow of security incident management through our ITSM system
QHSE Coordinator
To support our mission to provide effective and quantifiable energy solutions in a safe and sustainable manner, Welltec is strengthening the QHSE organization and actively recruiting for a QHSE Coordinator with a global role. This role will support our mission to provide effective and quantifiable energy solutions in a safe and sustainable manner.
The QHSE Coordinator provides continuous advice and support to ensure activities are conducted in accordance with internal and external requirements, promoting safe, reliable and sustainable solutions.
Manager, Chemical Substance Registration
The Manager, Chemical Substance Registration is accountable for implementing and executing the chemical control compliance programs of IFF in the EAME region (UK, EU REACH, Turkey REACH, EAEU etc.) for the technical enzymes’ portfolio of products (Biofuels, Fabric & Household Care, Textile Processing and Designed Enzymatic Polysaccharides).
The Manager, Chemical Substance Registration is furthermore a key contact for the Enzyme Business in determining strategic business decisions and should be representing IFF in industry work groups to assure IFF’s regulatory interests.
Project Manager - Mechanical Engineer
Are you ambitious, talented and eager to advance your engineering career in the medical device industry?
Senior Manager Health & Safety
Are you passionate about ensuring the well-being of personnel in design and construction activities?
Adv QA Professional in Device Development
Are you looking for an exciting opportunity to advance your career in Quality Assurance?
Manager, Environment & Sustainability
Are you a results-driven, strategic leader with a passion for environmentally sound solutions, based on a circular mindset and...
Safety Risk Manager - Medical Device Development
Are you ready to make a significant impact on Novo Nordisk's medical device development projects and contribute to enhancing the lives of our patients?
Construction Safety Program Manager
Are you passionate about ensuring the safety of construction projects?
Validation Specialist
Are you experienced in validation of Finished Product processes within the pharmaceutical industry?