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(Senior) Drug Substance Specialist
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.
Column Pack Operator
The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us. We’re growing our locations, our capabilities, our teams and looking for passionate, mission-driven people who want to make a real difference in people’s lives.
We are currently looking for candidates to work within Drug Substance Manufacturing (DSM) Support and become part of a newly established team, responsible for preparation, packing and qualification of chromatography columns.
Manufacturing Supporter
We are looking for a talented Manufacturing Supporter for the Drug Substance Production to join the DS Documentation and Support Department in Hillerød.
The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us.
You will be part of a team, consisting of 14 people, with a great sense of humor and a high willingness to support where needed.
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.
Quality Supporter
Har du øje for detaljen og fokus på kvalitet? Henter du samtidig energi via dialog og samarbejde? Så er du måske vores nye Quality Supporter.
Elopak Denmark A/S søger endnu et sæt kompetente hænder og et skarpt hoved til at supplere vores eksisterende laboratorieteam i kvalitetsafdelingen.
Vi tilbyder en attraktiv lønpakke med unik pensionsordning, sundhedsforsikring, personaleforening, tilskud til fitness, kantineordning, gode kollegaer, samt faglig og personlig udvikling igennem hele din karriere hos Elopak.
QC Instrument Engineer for QC Instrument Support
Are you energized by identifying and implementing automated and nimble solutions to help end-users?
Microbiologist in Quality Control - Maternity Cover (12 months)
Are you eager to join a fast-growing pharmaceutical company?