Clinical Pharmacology and Pharmacometrics (CPP) is an integrated part of the Global Development organization within Johnson & Johnson Innovative Medicines. We work in cross-disciplinary compound development teams and apply clinical pharmacology principles and pharmacometrics methodologies across the R&D portfolio to enable optimal decision-making in drug development at the earliest time point and in the most efficient manner.CPP Summer Internships are avai
Clinical Pharmacology and Pharmacometrics (CPP) is an integrated part of the Global Development organization within Johnson & Johnson Innovative Medicines. We work in cross-disciplinary compound development teams and apply clinical pharmacology principles and pharmacometrics methodologies across the R&D portfolio to enable optimal decision-making in drug development at the earliest time point and in the most efficient manner.CPP Summer Internships are avai
Job descriptionThe workstudy objective is to forecast shelf-life (physical stability) of anamorphous solid dispersion (ASD) in a tablet. This will be achieved by leveraging existingphysical stability data pertaining to the ASD powder. This will involve conducting DVS experiments on several physical mixturesASD/excipients, as well as in the tablet form, in order to understand water sorption/desorptionbehaviour of the tablet formulation. Additionally, a comb
Job descriptionThe workstudy objective is to forecast shelf-life (physical stability) of anamorphous solid dispersion (ASD) in a tablet. This will be achieved by leveraging existingphysical stability data pertaining to the ASD powder. This will involve conducting DVS experiments on several physical mixturesASD/excipients, as well as in the tablet form, in order to understand water sorption/desorptionbehaviour of the tablet formulation. Additionally, a comb
You will:* Mainly provide hands-on/lab-based support.* Prepare formulations in support of pre-clinical in-vivo studies. At later phase you might be involved in formulation development.* Run stability analysis (LC/UV MS) on the prepared formulations to check concentration and stability* Execute experiments to determine aqueous and biorelevant solubility and stability (pH, oxidation, light)* Performing assays to explore chemical and physical stability of AP
You will:* Mainly provide hands-on/lab-based support.* Prepare formulations in support of pre-clinical in-vivo studies. At later phase you might be involved in formulation development.* Run stability analysis (LC/UV MS) on the prepared formulations to check concentration and stability* Execute experiments to determine aqueous and biorelevant solubility and stability (pH, oxidation, light)* Performing assays to explore chemical and physical stability of AP
Job description:* 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
Job description:* 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