Role DescriptionThe Analytical Development department is responsible for the development of methods that are required for the analysis of vaccines for human use. Analysis includes testing for identity, quantity, potency, purity and contamination; in particular, extraneous agents safety.
ResponsibilitiesYou will be responsible for the extraneous agents safety of the products which the company develops and manufactures. Furthermore, you will ensure assay development and validation of various cell-culture based and/or molecular methods (e.g., mammalian cell culture, PCR, sequencing) for the analysis of in-process control and release samples to be conducted at GMP level in-house and at contract laboratories.
Demonstrating flawless documentation, effective communication with varied levels of the organization, a strong sense of responsibility and a passion for quality are key competences for this position.
Requirements- PhD degree or MSc with publications and excellent writing skills - minimal 2 - 5 years of experience with method development (microbiology - most relevant areas: prions/TSE, viruses, microbials, and/or cell biology - experience working with cGXP and/or other quality management systems - enjoys working in a multidisciplinary team
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Alexander Wielemaker.