Develop and optimize analytical methods to control and monitor chemical manufacturing processes and products
Plan and perform the development of analytical methods in a non-GMP environment.
Utilize developed analytical methods to generate data on development samples and prepare these methods for transfer to a GMP laboratory
Focus on Mixed Modality technologies, including Radioligand Therapies, Antibody Drug Conjugates, and Oligonucleotides
Maintain relevant laboratory infrastructure, ensuring that all equipment and tools are properly functioning.
Manage the inventory, ordering, and housekeeping of chemicals and reagents necessary for lab operations
Must Haves
1-2 years experience in method development of analytical methods in a relevant environment
Proven knowledge of relevant analytical technologies, such as HPLC / UHPLC including hyphenation with CAD, QTOF and other MS based detection. Further knowledge in GC / HS-GC, KF and other titrations systems etc. is desirable.
Proven experience in analysis of Mixed Modalities such as ADCs, peptides, Radioligand Therapy or Oligonucleotides desirable
Advanced knowledge of software and computer tools such as Office package, chromatography data-evaluation software (e.g. Chromeleon)
Good documentation skills required during execution of experiments and documentation of results