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Senior Project Manager

Are you motivated by being the driver of the implementation of new equipment/facilities or complex upgrading projects) up to EUR 15 million?

You will be responsible for and ensure project execution of all phases in your projects including scope definition, identifying the solution, and mitigating risks, time, budget, and quality. We primarily work with the stage gate model for our larger projects.

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.

Fleksibel og nysgerrig QA-koordinator med lederpotentiale

Kan du se dig selv stå i spidsen for at sikre høj kvalitet for mere end 1500 forskellige produkter årligt?

For Persano Group søger vi en QA-medarbejder, som kan se sig selv vokse ind i en ledende funktion, og som har den rette mængde af drive, nysgerrighed og ejerskab til at bidrage i en familiedrevet virksomhed, hvor stor passion er den kultur, der gennemsyrer virksomheden.

Downstream processing engineer – 12 months position

In this position you will be part of River Stone’s downstream processing (DSP) team, which is responsible for developing purification methods for our biological production processes for pharmaceutical ingredients.

The ideal candidate possesses:

• M.Sc. or Ph.D. degree in chemical engineering, food process engineering, chemistry, or similar
• Experience within down-stream purification processes, like solid-liquid separation, membrane filtration, crystallization and/or drying is a requirement
• Flair and motivation for hands-on laboratory work
• Ability to work in a fast-paced environment with deadlines and sometimes limited time for data analysis

Category Manager

Do you want to be responsible for developing our Sourcing of Packaging and Raw materials to new heights? Do you want to make a difference for patients undergoing surgery by securing the compliance of the medical devices used by healthcare professionals?

We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun.

Senior Category Manager

Here you have the opportunity to get an exciting and challenging job, as Senior Category Manager, in a international company. As Ferrosan Medical Devices is growing, you will be able to shape the job in our Strategic Sourcing Department to a large extent. The position refers to the Senior Manager of Strategic Sourcing.

We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.  

Quality Assurance Specialist

Would you like to be part of a strong and very skilled QA team supporting the qualification of GxP manufacturing equipment, facilities and utility systems?

You will be part of a well-founded team with 8 colleagues (4 Equipment qualification + 4 Environment) for Equipment qualification in QA Operations reporting to the QA Ops Manager for Qualification and Environment.

Continuous Improvement Partner

As a Continuous Improvement Partner in Drug Substance Manufacturing, you will be part of a team of Improvement Partners who develops and sustains systems and tools that enables the organization to consistently increase the level of operational excellence in manufacturing.

Your primary tasks will include but not be limited to:

• Develop and sustain CI systems and tools.
• Coach on ideal behaviour that drives a proactive improvement culture.

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.

Pharmaceutical Quality System Manager/Team leader

Are you a strong and visionary people leader – then please continue reading about this unique position.

Do you thrive in an environment where you have a highly skilled team to lead and spare with in locating the compliant solutions? And do you get energized by discussing ways to improve the processes with your team?

As a leading CDMO company, we are obligated to continuously improve our way of working, creating a dynamic and inspiring environment.

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

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.