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Lab Quality Coordinator, GCLP Laboratory

As Documentation Coordinator at the laboratory in Lund at MinervaX, you will play a central role in the establishment of a GCLP laboratory for clinical samples from MinervaX’s prophylactic vaccine targeting Group B Streptococcus (GBS). The GLCP laboratory is established to move into phase III clinical trials. You will be responsible for the writing, coordination, storage, and maintenance of documentation in the whole laboratory area.

This is a unique opportunity to join the journey into building a GLCP compliant laboratory. As this is a new position you can develop this role according to your own ambitions and will be primary person on documentation support.

QA Ext. Manufacturing Specialist

Would you like to work in one of the most interesting, complex, and dynamic areas in Bavarian Nordic? Are you ready to engage, support, and mobilize colleagues in a growing international business environment where we focus on saving lives every day?

As a QA Specialist, you will be responsible for daily support, QA oversight, and GMP guidance to Contract Manufacturing Organizations (CMOs) to ensure that our products are manufactured according to current GMP and our marketing authorizations.

Senior Research Technician

Do you want to work with data and HPLC analysis?

You will spend most of your time on HPLC analysis in our modern laboratory, which is designed to provide the best technologies and optimal working conditions.

Collaborating cross-functionally with our research scientists on both daily operations and projects, you will:

• Perform analytical method development in close collaboration with the responsible scientists
• Support formulation development studies with analyses

IT Infrastructure Engineer

As an IT Infrastructure Engineer at Zealand Pharma A/S, you will implement new infrastructure solutions and support existing systems.

Responsibilities include:

• Provides day to day support of overall infrastructure including network, physical and virtual servers, hypervisors, and storage platforms.
• Configures and implement new systems and enhancements to existing systems in support of business needs.

Senior Research Technician

Do you want to use your experience and problem-solving skills to work with pharmaceutical product development and early-stage development with a focus on characterization (MFI, DSC, HPLC)?

As a senior research technician, you will spend most of your time in the lab, where your primary role will be to prepare, plan, and perform pharmaceutical development work, including stability studies.

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.

Ambitious Global Business Intelligence Consultant with the abilities to drive and execute BI Excellence

As the Global Business Intelligence Consultant, you have the overall responsibilities for development and maintenance of the in-house elements of Pharmacosmos’ Business Intelligence and data platform in our US affiliate.

In the initial phase of the job, your role will primarily involve gaining a detailed overview of and analyzing the current extensive US data setup, the data landscape and data flows and technologies employed.

Ambitious Project Manager to lead key strategic projects

Are you an experienced Project Manager motivated by making a difference? Then look no further – Pharmacosmos is looking for a Project Manager who can solve complex problems across our value chain and deliver impact to the organisation.

As Project Manager, you will become a key member of a small project management team in Pharmacosmos. You will be allocated to important strategic projects that you will lead and drive to completion to the satisfaction of all involved stakeholders using your existing toolbox and competencies for managing projects.

Junior Controller

Er du detaljeorienteret, selvkørende og forstår regnskabets mange facetter? Så er du den vi leder efter. I Steelcos økonomiafdeling har de brug for en dygtig, engageret og positiv junior controller.

Du vil fungere som højre hånd til Nordic Finance Director og vil skulle supportere med controlling, rapporteringer og statistikker.Derudover vil en del af dine daglige opgaver blive:

• Daglig bogholderi, herunder kontering og bogføring
• Betaling af kreditorer
• Rykning af debitorer

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.

Clinical Trial Assistant

Are you looking for the possibility to unfold your competences within clinical operations even further? Do you thrive in an innovative environment working alongside dedicated clinical research professionals? Are you a self-driven team player, who enjoys a varied and influential day at work?

Pharmacosmos A/S is a progressive and innovative pharmaceutical company with headquarters in Holbæk, Denmark. We are on an exciting journey of global growth inventing new and innovative treatments, and right now we are expanding our team with a Clinical Trial Assistant.

Talent 2024: Start your career within Pharma & Life Sciences in CGI's MES/Automation talent program

Our most important task is to prepare you for the tasks you will solve. In cooperation with the companies that developed the systems, you will be certified in the technologies used, such as PROCOS, PAS-X and 800xA.

You will be involved in all phases of our projects, including sales support, consultancy, specification, design, engineering, construction, programming and testing, verification and validation, and commissioning with the end customer.

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.

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.

IT Administrator

Are you specialized in IT system administration?

Would you like to optimize and maintain our data centers, VMware setup as well as our backup services such as Veeam and Data Domain, and more? Are you process-minded with good attention to detail? Would you like to be a part of a dedicated IT Operations team in development?

Then you might be the IT Administrator we are looking for!

IT Administrator (Cloud)

Are you specialized in IT system administration of Microsoft cloud solutions? Would you like to optimize and maintain our Azure datacenter, as well as our Microsoft 365 services such as Exchange, Teams, SharePoint and more? Are you process-minded with a good attention to detail?

We are looking for a skilled IT System Administrator to:

• Help us implement new cloud-based solutions
• Take care of the administration

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

Data Engineer for Condition Monitoring and Machine Optimization

Do you want to play a key role in improving performance in the pharmaceutical and industrial manufacturing? Are you passionate about finding patterns in data?

You will implement our CATCH.AI data platform at our customers’ production sites and help them turn data into tangible actions and value.

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.

QA Engineer – ensure the quality of our software solutions for pharmaceutical drugs and devices

Do you want to play a key role in delivering software systems that are compliant to the pharmaceutical industry?

As Quality Engineer, you will work together with the project manager, the software developers and the customers validation teams and help secure that our solutions are compliant and lives up to the customers expectation so they can re-use our validation as their own.

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.