* You are responsible for the planning, coordination and execution of the analytical experimental work (method development, validation, transfer) the main part of this experimental work focusing on analytical methods for assay/purity, content uniformity, ID, moisture and solvents
* You independently lead multiple assigned projects: establishes priorities, checkpoints, and time frames in line with the project- and team objectives/deliverables
* You will collaborate closely with colleagues from analytical, API and Drug product development
* You advise and inform management and stakeholders of technical requirements, about potential scientific challenges and risks, prioritization or resources conflicts and makes suggestions to resolve or mitigate these
* You initiate ideas to improve the support and efficiency of the analytical method development/ validation/ transfer activities for the R& D portfolio
* You ensure that applicable guidelines, established operating procedures and safety regulations adhering to company work standards are being followed
* You author and review technical reports, protocols and standard operating procedures
* You maintain knowledge of Good Manufacturing Practices (GMP) and ICH Guidelines
Bedrijfsprofiel:
VOOR JANSSEN PHARMACEUTICA, ONDERDEEL VAN JOHNSON EN JOHNSON CAMPUS BEERSE, ZIJN WIJ OP ZOEK NAAR:
* In-depth technical knowledge and experience for developing/validating and transferring analytical methods in support of the R& D project portfolio with major focus on techniques as Liquid Chromatography (UHPLC), Mass Spectrometry (Single Quad) is required.
* Knowledge and/or experience with oligonucleotide/oligopeptide Analytical method development is preferred.
* Good knowledge of Dutch and English
* You can work independently, though you are also an excellent collaborator and like to work in a multidisciplinary, inter departmental and cultural divers context
* You can oversee projects in a professional way with respect to deadlines and with a good sense of urgency
* You ensure high scientific quality standards for experiments and take on responsibility for these experiments
* You are a prudent risk-taker, who thinks of innovative and creative solutions
You are available at short notice. Assignment for one year.
* Contributing to our mission to continue to bring transformational new medicines to patients for a world without disease. * Being part of a motivated and experienced research team in an innovative working environment * Through mentoring programs, e-university and on the job training, we ensure your personal development in a global company
a world without disease.
* Being part of a motivated and experienced research team in an innovative working environment
* Through mentoring programs, e-university and on the job training, we ensure your personal
development in a global company