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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.

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.

Quality Assurance Specialist

Er du god til at gøre krav og regler meningsfulde og forståelige over for dine kollegaer? Så har vi en spændende stilling i vores QA-afdeling til dig.

Quality Assurance er en central og vigtig del af vores værdikæde. Einar Willumsen (EW) er certificeret efter BRC Standard for Food Safety, og din opgave bliver at medvirke til at sikre en fortsat høj standard med stort fokus på kvalitets- og fødevaresikkerhedskultur.

Vi tilbyder et spændende og udfordrende job i en kultur, hvor samarbejde vægtes højt. Du bliver en del af en international virksomhed med mange muligheder for personlig udvikling. Og en ting kan vi love: det bliver aldrig kedeligt.

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.

Manager Virus Production

Do you want to play a central and important role in Bavarian Nordic´s manufacturing strategy by setting directions and ensuring smooth daily operation in our production facility?

Our newly established Drug Substance Facility in Kvistgaard will soon start production ramp-up, and we therefore need to strengthen our leadership. You will become responsible for the day-to-day shopfloor management of 15-20 operators.

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

Senior Specialist til QC hos Xellia Pharmaceuticals

Drømmer du om mere ansvar, med forskelligartede opgaver, og har du en passion for mikrobiologi? Vil du spille en central rolle i Xellias produktionen af livsvigtig antibiotika?

Som senior specialist vil du blive faglig ansvarlig for vores count release-laboratorie, som bl.a. udfører TVC- og LAL-analyser. Derudover vil du indgå i tæt samarbejde med vores sterile produktioner angående EM, hvor de nye Annex 1-krav stiller øgede krav til vores compliance, som du vil spille en vigtig rolle i.

Application Specialist – Beverages

Are you passionate about product development within all types of beverages from premium organic CSD's to flavored spirits?

You will work in a high-paced, collaborative and energetic environment optimizing key elements of beverage applications such as taste, stability, preservation and appearance with the goal to design the perfect balance between these elements.

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.

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.

Ingeniør til validering

Vi har brug for en konsulent til et spændende job indenfor kvalificering og validering. Stillingen byder på mange forskellige opgaver og projekter hos vores kunder på det meste af Sjælland, og du får en spændende, travl og varierende hverdag.

Du vil bl.a. koordinere, planlægge og udføre validerings- og kvalificeringsprojekter, som kan omhandle: rengøringsvalidering, sterilisationsprocesser, procesanlæg, IT-validering, klimafaciliteter, produktions-, måle- og laboratorieudstyr.

Regulatory Affairs Specialist

The RA Specialist for Radiometer is responsible for ensuring coordination of regulatory activities for a few of our Blood Gas products manufactured in California to help ensure continued compliance in all markets.

In this role, you will have the opportunity to:

• Facilitate coordination of regulatory activities between California and Denmark for design control activities and international registrations for a few of the instruments/consumables manufactured in our California site.
• Ensure compliance with EU regulations.
• Generate STED files, international submissions & assess design changes.
• Plan and execute projects for new regulatory requirements.

Senior Regulatory Specialist

The Senior Regulatory Affairs Specialist at Radiometer is responsible for collecting and generating documentation for product submissions to ensure compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world.

If you thrive in a fast-paced environment, are used to playing a critical supporting role and want to work in a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.