Associate scientist SMMD - Beerse, België - Johnson & Johnson

Beschrijving

• Responsible for the coordination and execution of the analytical work (method development, -validation, -transfer) to be done in support of assigned projects and tasks, with a primary focus on the relevant quality attributes of the active pharmaceutical ingredients (API's), drug products (DP's) as well as raw materials/intermediates, and this using a variety of analytical techniques, such as Liquid chromatography, Gas chromatography, Titrations and KF water determinations.
• Manages multiple assigned projects and tasks, while establishing the right priorities in line with project/customer requirements and agreed timelines.
• Informs supervisor about potential technical/scientific challenges and risks, prioritization or resources conflicts.
• Reviews the scientific data and assists the AD-SMMD scientists in summarizing/interpreting the data and in drawing conclusions.
• Responsible for GMP documentation of generated data and protocol/report writing.
• Ensures that applicable guidelines, established operating procedures and safety regulations adhering to company work standards are being followed.
• Review, interpretation and reporting of the obtained analytical data.
• Works closely with the scientists of AD-SMMD and other partner departments to ensure fit for purpose analytical work and reporting.