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Ferrosan Medical Devices A/S

Senior Process Specialist

Søborg

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.

Zealand Pharma A/S

(Senior) Drug Substance Specialist

Søborg

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.

Zealand Pharma A/S
Ferrosan Medical Devices A/S

Senior QA Specialist

Søborg

You will be part of our QA Business Support Team, consisting of 12 QA Specialists and Senior QA Specialists, allocated to projects including innovation projects, capacity projects and strategic QA/QC projects. We participate in projects both as quality and compliance experts to ensure compliance with the requirements for Class III Medical Devices.

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.

ROI Consulting A/S søger for Artelia
Gem
ROI Consulting A/S

Lead Automation Engineer til Pharmadivisionen

Søborg, Vipperød eller Kalundborg

Har du en god procesforståelse og erfaring med at arbejde i pharmabranchen, kan du måske se dig selv som Lead Automation Engineer i Pharmadivisionen.

Vi søger to nye kollegaer med en stærk automationsfaglig erfaring og kendskab til at arbejde med sterile processer. Du bliver en del af afdelingen: C&Q/Automation – en nyere afdeling som vi er godt i gang med at opbygge. På nuværende tidspunkt består den af syv dedikerede medarbejdere, der arbejder med commissioning, automation og test af anlæg. Her vil du indtage en central rolle som specialist på automationsområdet, og du vil få rig mulighed for at være med til at udvikle C&Q/Automation-afdelingen.

ROI Consulting A/S søger for Artelia
Gem
ROI Consulting A/S

Senior Commissioning & Qualification Engineer

Søborg, Vipperød eller Kalundborg

Vi søger en Commissioning & Qualification Engineer, der elsker at blive udfordret inden for sit fag, og som deler vores passion for at arbejde med pharma.

Du vil komme til at arbejde med projekter inden for idriftsættelse, test og fejlfinding på anlæg - hovedsageligt på projekter i pharmasektoren. Stillingen berører stort set alle aspekter inden for idriftsættelse, og det er vigtigt for os, at du har en solid erfaring med maskin- og processtyring samt praktisk idriftsættelse.

Du får rig mulighed for at være med til at præge udviklingen af afdelingen, hvor vi gør en stor indsats for at skabe et godt sammenhold i en travl hverdag.

Zealand Pharma A/S

Regulatory Affairs Clinical Specialist

Søborg

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.

Zealand Pharma A/S
Ferrosan Medical Devices A/S

SAP Master Data Specialist

Søborg

Do you want to be a part of Process Support in a company with a unique impact on global healthcare?

You will be coordinating SAP production master data activities throughout the organization in order to achieve safe and predictable product implementation, maintenance, and decommissioning.

Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.

Gem
Orifarm

Specialist, Regulatory Affairs (Temporary Position)

Odense S and Søborg

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
Orifarm
Ferrosan Medical Devices A/S

Training Partner

Søborg

Are you passionate about designing high impact training to improve ways of working?

The role will focus on re-designing the training related to onboarding our professionals working directly with our operation, our Operators, and our Laboratory Technicians.

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.

Amgen Denmark

Senior Engineer Device Manufacturing

Søborg

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.

Experienced GMP Partner

Søborg

Are you passionate about compliance, structure, and continuous improvements?

Indrykket:

Manager of Safety Surveillance Early Development

Søborg

Do you want to play a key role in driving the ongoing safety surveillance activities for early development projects in Novo Nordisk?

Indrykket:

Senior International Medical Manager

Søborg

Are you a Medical Doctor with an interest in clinical development of pharmaceutical drugs, medical devices and digital health?

Indrykket:

Senior Regulatory Affairs CMC Professional

Søborg

Do you have experience from either RA, CMC, QA, and/or QC – or any other relevant area?

Indrykket:

Senior Regulatory Affairs Professional

Søborg

Do you want to play a key role in accelerating the development of our patient-focused products?

Indrykket:

Scientific Publications Manager

Søborg

If you have a great interest in scientific communication and enjoy interacting with global key opinion leaders in a dynamic working environment, then please read on!

Indrykket:

Clinical Pharmacology Specialist

Søborg

Are you passionate about clinical pharmacology and drug development?

Indrykket:

Data Science Policy Specialist in Regulatory Affairs

Søborg

Do you want to work with policies and regulation on advanced data science capabilities and methodologies?

Indrykket:

Regulatory Policy Professional

Søborg

Join a fast-changing environment where people do their best to get Novo Nordisk products approved across the globe.

Indrykket:

Senior Director, Portfolio Regulatory Policy

Søborg

Are you passionate about shaping future regulatory frameworks and policies?

Indrykket:

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