QA Assistant

Motiveres du af en stilling, hvor du har fokus på systemer og kvalitet? Og vil du arbejde med fremstilling af pakkematerialer til den farmaceutiske industri?

Du vil få daglig sparring med operatører, specialister og ingeniører i vores produktionsenhed i Horsens – som årligt producerer ca. 2,5 milliarder enheder.

Vi tilbyder en spændende stilling med mulighed for at sætte dit personlige præg på måden, tingene fremadrettet skal gøres på.

Clinical Scientist

Join GE HealthCare to help develop our growing team in Clinical Development. This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

Our main responsibilities are to drive clinical strategies successfully, i.e., leading and maintaining products throughout their entire life cycle management.

We are an international team who values cultural and personal diversity in an informal, friendly, and respectful atmosphere.

Administrativ laborant

I prøvemodtagelsen registreres alle laboratoriets prøver, kemiske såvel som mikrobiologiske. Der er i prøvemodtagelsen ikke noget analytisk arbejde.

Vi søger en kollega med et stærkt udviklet servicegen, som vil bidrage til teamet. Dine arbejdsopgaver vil bestå af modtagelse, registrering, auditering og distribution af indkomne prøver samt afvigelsesbehandling.

Du vil blive en del af et engageret team på 5, hvor tingene ofte går stærkt, men hvor der også er tid til humor.

Specialist in iPSC Derived T Cell Generation and Modulation – DTU Health Tech

If you are a specialist with interest in stem-cell differential and immunology and T cell driven immunotherapies this project employment is a great opportunity.

We are looking for a skilled and experienced specialist who will be responsible for establishing, optimising and using a process/protocol of iPSC-derived T cell maturation.

The position is part of the DigitStem project, a larger collaboration between Bioneer and DTU, specifically focusing on the development of iPSC derived cell products for clinical use, as cell therapy products for cancer treatment.

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.

TS Research Associate; Lab Team DK, Lyngby

Do you want to work in an environment in which creativity, business drive and scientific excellence all thrive?

You will become part of our dynamic Research Associates team within the European Technical Service Team that provides technical support and innovative solutions to Novozymes’ customers within the bioenergy, biodiesel, degumming, distilling, grain milling and starch industries, working closely with our industrial specialists and scientists.

Manager for a Project team

Are you ready to take on a leadership role and guide a team of experienced project managers and skilled specialists toward achieving new levels of success?

We are seeking a dedicated people manager to fill this crucial position within our dynamic project and process team, focusing on Drug Product technical support at our manufacturing site.

Laborant til mikrobiologisk team

Har du lyst til at være med til at sikre vacciner til forebyggelse af infektionssygdomme?

Bavarian Nordic er i en rivende udvikling og derfor søger vi en laborant til det mikrobiologiske team i Kvistgaard. Du vil i stillingen bidrage til test og frigivelse af vacciner mod kritiske sygdomme. QC-mikrobiologi har ansvaret for at udføre analyser af rutine prøver og valideringer af nye produkter. Desuden yder vi support til vores produktion.

Business Supporter for product documentation in Human Health

Would you like to be part of a forward-thinking organization dedicated to advancing Human Health? The Global Business Support team is looking for a new colleague who will play a key role in the management of product documentation within Human Health.

You will be overseeing product documentation and you will have an important role in managing and maintaining documentation for new product implementations as well as for existing products. You will support daily product-related queries, optimize internal processes, and engage in stakeholder training.

Clinical & Product Training Manager (EMEA/Asia) to GE HealthCare Denmark

This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.

Our global Clinical and Product training team consists of fifteen dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities.

We are a strong team that values collaboration, support, honesty, and respect. We are driven by making a difference and continually improving training activities across the globe.

Apotekskonsulent til Jylland/Fyn

Brænder du for apoteksbranchen og for at vedligeholde og udvikle kunder i en tæt kundedialog? Kan du arbejde selvstændigt og tage ansvar for egen læring og for egne resultater?

TMJ søger en kollega med fagligt kendskab til branchen til vores salgsafdeling.

Du tilbydes et job med ansvar for at servicere og udvikle vores kunder primært i Jylland og på Fyn. Du bliver således en del af et dygtigt salgsteam med 3 kolleger, hvor der er fokus på et tæt samarbejde og vidensdeling.

PhD scholarship in Clinical Assessments of Vestibular Balance Disorders and Rehabilitation – DTU Health Tech

Are you interested in combining clinical medicine and engineering to help create better healthcare for individuals suffering from vertigo?

This PhD project focuses on clinical assessments of patients with vertigo, with a focus on benign paroxysmal positional vertigo. The aim is to supplement existing diagnostic tools with more objective and valid estimates of balance assessment to improve decisions on relevant diagnostic pathways and treatment, as well as to facilitate more effective counselling and expectation management regarding balance rehabilitation.

Nanofabrication Technician to state of the art laboratory

We are looking for a Nanofabrication Technician for our client’s brand new, state of the art, semiconductor and fabrication laboratory in Copenhagen. The lab is among the largest in Europe and you get to work with cutting edge technology in a highly dynamic environment of scientist, researchers and engineers trying to push the boundaries of computing.

Material science and fabrication are the foundation and the enablers of qubit devices. In their research, our client deals with complex stacks of different materials, combined at the nanoscale, and require high repeatability of fabrication processes.

Analytical Chemist at NCK A/S

Do you thrive in a dynamic work environment where you can take responsibility and contribute to patient safety? Are you ready to develop new analytical methods for new drug candidates?

As part of our competent QC team consisting of seven people (laboratory technicians and academics), you will develop and validate new analytical methods in accordance with the ICH guidelines and also perform laboratory work – both independently and in collaboration with other laboratory technician

QA Manager

Your success will depend on your ability to excel as an inspiring, supportive, and motivating leader, while effectively managing stakeholders in a complex and dynamic organization.

You will

• Provide leadership and inspire continuous development of the team members through coaching and dialogue.
• Lead the quality team and ensure high motivation and work-life balance.

Lægemiddelrådgiver med indgående kendskab til lægemiddelområdet

Har du et indgående kendskab til lægemidler og lægemiddelmarkedet? Brænder du for at holde øje med, hvilke nye lægemidler, som er på vej på det danske marked?

Som lægemiddelrådgiver bliver en af dine opgaver at have overblik over hvilke lægemidler og indikationsudvidelser, der inden for de kommende to til tre år forventes at blive markedsført i Danmark.

Investment & Maintenance Specialist to Nordic Sugar

Would you like to work in a hugely automated process industry that produces several million tons of sugar and animal feed made from sugar beet?

As our new colleague, you will participate in key projects that support our business needs. Specifically, you will:

• Developing and supporting Go Green and I&M projects from planning to commissioning together with the plants or departments
• Managing projects incl. monitoring budgets

Regulatory Affairs Specialist

We are on an exciting path of growth and are currently seeking a new specialist to join our team and play a crucial role in ensuring that our operations adhere to relevant regulations and industry standards.

A significant part of your role will be to take regulatory ownership of selected product areas, and ensure the required activities take place, to ensure we are following current regulatory standards for medical device development.

Struer Apotek søger farmakonom

Er du uddannet farmakonom, eller bliver du færdiguddannet til sommer? Vægter du, ligesom os, et godt kollegaskab samt et fagligt miljø højt?

Struer Apotek har nemlig netop nu mulighed for, at tilbyde et spændende og alsidigt farmakonomjob.

Vi er et apotek, som dagligt har en masse forskellige og spændende opgaver. Alle farmakonomer har deres egne ansvarsområder, hvilket gør at dagene hos os aldrig er ens.

På Struer Apotek kan man i høj grad selv få indflydelse på arbejdsopgaver og arbejdsskema.

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.