Production Assistant

We are looking for a skilled, purpose-driven Production Assistant to join our production team in Hellerup, DK.

You will be at the heart of our production operations, engaging in a diverse range of tasks from packaging orders and improving production processes to solving cross-departmental issues and liaising with suppliers.

You will also take on the role of superuser for our production IT systems, including Navision (ERP), Master Control (QMS), and BarTender/PrintStation (label system).

Supplier Quality Engineer

We are looking for a Senior Supplier Quality Engineer to join our team. The main responsibilities include ensuring compliance with various Regulations and Standards, leading Supplier Quality Compliance Projects, developing Partner Quality Agreements, managing high visibility SCARs, and conducting key Supplier Audits.

If you have expertise in Supplier Quality and a passion for process improvement, we want to hear from you!

PhD scholarship in Future Marine Food Innovation - DTU National Food Institute

The DTU National Food Institute is offering a PhD scholarship focused on advancing marine foods and ingredients.

We are seeking a candidate with master’s in food science, food technology, or similar, who understands the complexity of foods, including food chemistry and physics, and is passionate about changing “the way we SEA food”. Your primary goal will be to enhance the Department's expertise in advising on future foods by anticipating trends in the expanding market of novel foods.

External Account Manager Pharma

I Brenntag’s danske Essentials forretning søger vi en ny External Account manager indenfor Pharma. Vores Essentials forretning håndterer basiskemikalier til alle industrier.

Din rolle og ansvar vil bl.a. være:

• Resultatansvar for Pharma-kunder i Danmark.
• Kundeansvar omfatter servicering, salgsudvikling og opbygning af professionelle relationer til nye kunder og eksisterende nøglekunderelationer inden for Pharma-segmentet.

Process Management Manager

Er du klar til at tage ejerskab for vores Process Management Team og være med til at forme fremtiden for diagnostisk produktion i en formålsdrevet virksomhed? Har du erfaring med at lede et team inden for et reguleret område som IVD eller medicinsk udstyr?

Som leder af teamet har du ansvaret for den daglige ledelse, trivsel og udvikling af teamet. Du deltager aktivt i leverancerne og ser dig selv som en 'spillende træner', der nyder hverdagen i teamet på sitet.

Farmakonom søges til Kundeservice

Vil du gøre en forskel i en dynamisk og spændende virksomhed i medicinalindustrien? Vil du have udfordrende og varierende arbejdsopgaver, og trives du i en virksomhed i forandring?

Så har vi et spændende job til dig!

Vi søger en farmakonom – med kendskab til apotekets dagligdag – til at indgå i vores team af kundeservicemedarbejdere. Har du en stor interesse for kundeservice, så er det måske dig, vi søger!

QA Auditorer

Da Scantox er i stor vækst, søger vi QA-auditorer til vores afdeling i Ejby, som også understøtter vores datterselskaber. QA-afdelingen arbejder uafhængigt af resten af organisationen og leverer kvalitetssikring i dyrefaciliteten og laboratorierne, til den øverste ledelse og til vores kunder.

Du vil bl.a. gennemgå studieplaner, rapporter og andre regulerede data og sikre overholdelse af gældende regler, internationale standarder og procedurer, samt interne SOP’er.

Product Manager – Drive innovation and product leadership in a fast-growing international life sciences company

You’ll be the vital link between strategy and execution — the “spider in the web” — turning our commercial strategy into actionable goals.

You’ll play a pivotal role in product development, documentation, and lifecycle management, leading initiatives that combine scientific insight, creativity, and commercial drive.

Senior/Lead CSA Consultant

As a Senior/Lead Consultant within CSA (Civil, Structural, and Architectural) or as a Clean Room Architect at Emendo Engineering, you will play a central role in delivering complex engineering projects within the pharma and life science industry.

You will lead technical work packages or take on overall project management responsibilities throughout the project lifecycle — from design and tendering to construction, qualification, and commissioning.

Senior Regulatory Writer

Are you ready to take up an important role in a global organisation marked by entrepreneurial spirit, a strong innovation pipeline and substantial growth?

You will be responsible for driving and coordinating regulatory approval relevant activities and projects, including but not limited to authoring, reviewing and coordinating regulatory documentations for approval applications on AFI’s products to gain market access.