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See your Job AgentsSenior Research Technician
Do you want to work with data and HPLC analysis?
You will spend most of your time on HPLC analysis in our modern laboratory, which is designed to provide the best technologies and optimal working conditions.
Collaborating cross-functionally with our research scientists on both daily operations and projects, you will:
- Perform analytical method development in close collaboration with the responsible scientists
- Support formulation development studies with analyses
Senior Research Technician
Do you want to use your experience and problem-solving skills to work with pharmaceutical product development and early-stage development with a focus on characterization (MFI, DSC, HPLC)?
As a senior research technician, you will spend most of your time in the lab, where your primary role will be to prepare, plan, and perform pharmaceutical development work, including stability studies.
Clinical Project Manager
Do you want impact, freedom to perform, global perspective and super colleagues?
As experienced Clinical Project Manager, you naturally know that your success is built on your ability to generate high quality data at high pace and within agreed budgets – without jeopardizing the good relationship to the people and partners involved. Another vital part of your road to success is your ability to think outside the box and handle (unforeseen) challenges on the way.
Kemiker til QC med GMP-erfaring
Syntese A/S søger en erfaren kemiker med kompetencer og interesse for analytisk kemi og GMP. Stillingen er en udvidelse af nuværende team.
Dine primære opgaver er at indgå i afdelingens daglige drift, hvor du supporterer og godkender analyser i et tæt samarbejde med dine kollegaer i teamet. Du udarbejder afvigelser, opdaterer SOP´er og vedligeholder kvalitetssystemerne.
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.
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