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Senior Product Test Engineer - Medical Devices

Do you want to design safe and reliable medical devices, bringing our clients' life-changing solutions into the hands of patients and helping patients to get better treatment?

You will be an essential contributor in the development and designing optimal verification methods for requirement confirmation.

We seek to enable the best work environment that helps you and the business work together to produce superior results.

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

Food Technician - Arhus

Are you passionate about turning ideas into concrete products via your hands-on technical skills?

As Food Technician you will be the prime responsible for running pilot scale trial-production of a wide range of dairy/’plant based’ products. Your work will always happen in close collaboration with product developers/food designers. To be more specific, you will:

• Perform pilot trials within a wide variety of product and technology areas
• Contribute to the preparation of the test proposal and help plan the trials

Coop Trading is looking for a technical expert to handle cosmetics and personal care products

Do you have a technical background within chemistry or pharmacy, and are you curious by nature to learn more, e.g. about developing products for retail?

You will develop an attractive and competitive personal care and cosmetic product portfolio for the Nordic Private Brand market in close cooperation with the team and suppliers. You wil also quality assure that the portfolio complies with Coop's high standards within safety, sustainability, consumer information and quality.

Senior Engineer Device Manufacturing

Are you passionate about cutting-edge medical technology? Do you thrive in a collaborative environment where innovation drives patient care?

Amgen, a global biotechnology leader, is expanding its device development capabilities in Denmark and is seeking a talented Senior Engineer to join our Device Engineering group.

Project Coordinator

Do you have experience managing projects anchored to a GMP facility? Are you eager to contribute to the development of a newly established project team in a production environment?

As a Project Coordinator, you will participate in the successful planning and completion of projects related to the Drug Substance Manufacturing Processes. You will coordinate and follow up on a number of tracks that links to various projects.

Engineering Project Manager

Har du en passion for at drive teknologisk udvikling og bruge dine kompetencer i den grønne industrielle omstilling?

Den succesfulde kandidat vil have en ledende rolle i ALGIECEL's full-scale demonstrationsprojekt, der transformerer CO2-emissionerne på Novonesis' faciliteter i Kalundborg til bæredygtige algebaserede produkter gennem en yderst effektiv og kompakt fotobioreaktor.

Tiden for forandring er nu, og dette er din chance for at blive en del af vores højt motiverede team!

Protein Chemist for production of antibodies for cancer diagnostics

Do you find antibody production exciting?

You will play a key role in daily support of the production of conjugates. This can include:

• Support lab techs in case of technical issues with purification, conjugation, and test of antibodies.
• Handle compliance issues according to GMP standards.

We offer a high degree of freedom and development opportunities in an international company.

Clinical Site Manager

Are you looking to make a significant impact on ensuring oversight of our outsourced clinical studies in Ferring Pharmaceuticals? Do you thrive in a global role that requires cross-functional collaboration?

In this role you will solidify the implementation of the Clinical Site Manager role. This role was recently introduced as being responsible for providing sponsor oversight of clinical site monitoring (outsourced to a CRO) and establishing strong relationships with clinical sites to ensure delivery of high-quality and timely clinical trials.

In this role you will be working closely with counterparts in the US and stakeholders at our International PharmaScience Center (IPC) in Copenhagen.

CTS Proposal Manager

Join an international drug development consultancy and contribute with strategic advice and operational support to clients based in Europe, the US and Asia.

You will be part of a dedicated proposal team adding unique and highly valued competencies to the proposal process in CTS, supporting and underlining our professional cooperation with present and future clients in all parts of the world.

Our Proposal Managers work closely together with all parts of the organisation and represents the anchor of our client dialogue both in initial phases and as support throughout the client-life-cycle.

Analyst and Project Coordination In Life Science Consultancy

Would you like to work with data analysis and research of worldwide trends in the pharmaceutical and biotechnological industries?

You will get the responsibility of managing and coordinating the day-to-day operations needed to solve our projects and writing reports for our commercial unit.

An academic background in life science (pharmacy, biotechnology etc.), economics or similar is required.

Area Sales Support Manager

You will be responsible for specific markets, building and maintaining relations with customers, negotiating sales and facilitating the growth potential in your markets for the sales of ice cream equipment.

We offer you

• A variety of exciting challenges with ample opportunities for development and training in a truly global landscape
• Market competitive compensation and benefits with flexible working arrangements

QA Academic CMC Development

Do you want to be part of an agile, inspiring, and competent team while restoring brain health for patients worldwide?

Then join us as our new QA Academic, ensuring product quality while collaborating with multiple stakeholders leveraging your professional and personal competencies. We offer an exciting job with a broad variety in you daily work supporting CMC deliverables from early to late phase pipeline projects.

Technical supporter within quality and documentation

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?

We are looking for a colleague to join our process support team. The team is responsible for running pilot and demonstration scale fermentations and downstream operations. These days we are implementing GMP+ in our production, and we need your experience to support this process and maintain the system afterwards. In your daily work you will support management and process in updating and reviewing process documentation, coordinating training activities, and handling deviations.

Drug Substance Production Supporter

Our vaccines make a real difference to people, and no matter your role we all contribute to protecting lives every day. In Virus Production Support team your main area of responsibility will be:

• Trouble shooting in production
• Process confirmation to ensure your processes are running according to written procedures

Specialist QA Record Management

Do you have solid experience with electronic Document Management Systems (EDMS), Data Integrity, and record-keeping policies and systems?

Our vaccines make a real difference to people, and no matter your role we all contribute to protecting lives every day. This is how your work matters:

• Act as process manager for the Record Management process
• Responsible for how our EDMS systems work
• Responsible for how our physical paper archive system works

Sr. Project Lead, DSM expansions Go-Live

Are you seeking a new and exciting challenge in the Biopharmaceutical Industry?

Your primary tasks will entail but not be limited to driving the successful execution of project deliverables, facilitating workshops, and drive the realization of project track.

Join us and discover a community that thrives on diversity and never scares away from a complex challenge. At FDB, you determine what’s possible.

Senior Data Manager

The Senior Clinical Data Manager is responsible for leading and overseeing data management activities associated with clinical trials, ensuring data accuracy and consistency, and managing data cleaning and quality control processes.

We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.

Clinical Supply Manager

The Clinical Supply Manager will be managing outsourcing of packaging, labelling, and distribution of clinical trial supplies for all clinical trials.

You must have extensive knowledge of cGMP and have a focus on the level of quality in work performed.

We strongly endorse a flexible working environment around its core working hours of 09:00-15:00 and endorses fair and equal pay practices.