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Kundeservicemedarbejder

Har du en sundhedsfaglig uddannelse som farmakonom, sygeplejerske eller tilsvarende, og kan du lide en hverdag med masser af kontakt med kunder via telefon, mail og chat?

Dit daglige arbejde vil primært være kontakt med kunder i Danmark via telefon, mail og chat, hvor en stor del af henvendelserne drejer sig om diabetesprodukter. Kontakten med kunderne indrapporteres i vores kvalitetssystem og du står for både kontakt, indrapportering og opfølgning overfor kunderne.

Du bliver en del af et team, der servicerer både sundhedspersonale og private kunder. Vi arbejder med fastsatte mål og KPI´er med henblik på at sikre, at vi lever op til vores høje kvalitetsstandarder.

QA-specialist, der er QP-delegeret eller drømmer om at blive det

Drømmer du om at bidrage til at sikre kvaliteten af livsvigtige lægemidler, der redder liv? Er du en erfaren kvalitetsspecialist med erfaring fra lægemiddelproduktion?

Som delegeret Qualified Person (QPd) i vores Manufacturing QA (MQA) afdeling får du en unik mulighed for at arbejde med kvalitetssikring og frigivelse af Xellias produkter. Du vil være med til at sikre, at vores antibiotika når frem til patienter i hele verden i den højeste kvalitet. Som delegeret QP hos Xellia får du et stort ansvar.

Lead Automation Engineer til Pharmadivisionen

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.

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.

Automationsingeniør med erfaring indenfor Pharma

Vil du arbejde med spændende og varierende projekter indenfor automation og kunne du tænke dig at blive del af et dygtigt tværfagligt team, hvor humøret og ambitionerne er tårnhøje?

Vi arbejder i Pharma automation teamet dedikeret med design, programudvikling, indkøring, test og kvalificering af procesløsninger til vores pharma og biotech kunder og du bliver således en del af vores tværfaglige projektteams.

På kontoret i Kalundborg vil du indgå i et professionelt fagmiljø, hvor der er fokus på vidensdeling og det gode samarbejde. Din dagligdag bliver præget af gode kollegaer, faglige udfordringer og stor medbestemmelse.

Business Developer with a background in Science

Do you want to be at the forefront of Targeted Radiopharmaceuticals and Molecular Imaging?

We are looking for a professional Business Developer with a background in life sciences and the ambition to contribute to further strengthening Minerva Imaging as the trusted partner for targeted radiopharmaceuticals and molecular imaging.

What truly matters is your passion for the advancement and know-how of our scientific studies and your ability to foster long-term relationships with our collaborators.

QC-medarbejder med passion for IT

Du vil være QC’s nøgleperson i LIMS-projektgruppen hvor vi skal implementere LabVantage som vores LIMS-system.

Du vil være ansvarlig for at implementere og understøtte designet af vores LIMS-system ved at oprette og vedligeholde de mesterdata, som udgør rygraden i vores LIMS.

Hos os får du en chance for at være en del af et dedikeret og talentfuldt team i en organisation, hvor professionalisme møder passion. Vi vægter dog også en god portion humor i dagligdagen.

Manufacturing Associate - Operator

We are looking for process operators, preferably with experience from a similar pharmaceutical production company or similar regulated businesses OR a Life Sciences Graduate who have recently finalized their Bachelor or Master degree relevant for Biologics Manufacturing and are keen on starting their career in a manufacturing and international environment where things move fast.

We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools.

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.

SAP Master Data Specialist

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.

Kvalitetskoordinator

Motiveres du af at arbejde med fødevaresikkerhed, projektledelse og udvikling, og har du interesse for fødevarer, hvor råvarer, smag og næringsværdier er i højsædet?

Du bliver en nøglespiller i kvalitetsteamet og bliver ansvarlig for vedligeholdelse og opdateringer af specifikationer og varedeklarationer. Du bliver også involveret i kundeprojekter, når nye råvarer og recepter skal implementeres.

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.

Specialist, Regulatory Affairs (Temporary Position)

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

Kvalitetskoordinator til NORDEX FOOD

Nu har du muligheden for at blive en del af et fantastisk 5 kløver af dedikerede, energiske og pragmatiske kolleger, som brænder for kvalitetsarbejde.

Kvalitetsteamet består i dag af Heidi, Simon, Sanne, Morten og Camilla. Vi søger en barselsvikar som, efter en periode med et "overlap", kan tage over på Camillas opgaver, når hun går på barsel til september.

Dine primære arbejdsopgaver

• Vedligeholdelse af kvalitetsstyringssystem (procedurer, instrukser, politikker)
• Samarbejde med fødevaremyndigheder

QA Specialist

We are seeking a competent new colleague to join our QA team in a dynamic and growing company.

You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.

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.

Application Technician – Food Ingredients

We are looking for an employee with an interest in laboratory and food technology to assist in the AKV FoodLab in Aarhus, where you will become part of the team.

Here you will play an important role in relation to taking part in the ongoing laboratory work with a confident and collaborative team approach.

As an Application Technician in AKV FoodLab, your primary tasks will consist of:

• To assist the Senior Application Specialist with research by running trials of a broad range of applications in the FoodLab and conducting analysis and characterization of food products.
• Maintenance and cleaning of process equipment.
• Contribute where required in purchasing tasks for the FoodLab.

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.

Technician, EMA Solids Support Team

Welcome to Solid Support Team 13 skilled process engineers and technicians responsible for quality, introducing new products, throughput, and optimizing the products.

In this role you’ll make an impact by:

• Responsible technician for the MG-coating line, ensuring smooth and efficient coating processes for granulating with MnTACN
• Coordinate the steering system changes, bridging the gap between process engineers, technicians, and programmers to optimize operational efficiency.

Driftsleder/Procesleder til industribageri

Er du klar til næste skridt i din karriere inden for produktion?

På bageriet i Avedøre søger vi en procesleder, der vil være med til at sikre en stabil produktion. Du får ansvaret for driften i bageriet. Personalet dækker ca. 15 faste medarbejdere.

Du går forrest, evner at arbejde på tværs og skabe opbakning hele vejen rundt. Og dit fokus på udvikling af processer skaber succes i stillingen.