Typical Accountabilities: • Manages own work to achieve drug and improvement project targets in a timely fashion and to agreed quality standards by applying technical knowledge and expertise • Aids with the selection of candidate drugs from a product design perspective • Conducts experimental work to characterise and understand the pharmaceutical properties (physicochemical and biopharm) of drug substances and formulations • Develops formulations and manufactures batches for discovery, pre-clinical or clinical use as required, as well as developing and validating appropriate test methodology and specifications for these • Develops drug substance route and process for early supply including identification of ‘C-2' synergies • Assesses and reports data with a clear understanding of its reliability and interprets findings and draws authoritative conclusions and recommendations so that their significance can be appreciated • Provides technical instruction to team and allocates administrative work where possible • Applies technical knowledge to improvement projects and the evaluation of new technology/processes • Collaborates with specialist scientific and/or technology networks within Pharmaceutical Development • Presents information for discussion at team meetings • Works as a member of cross-functional teams, representing own department or area of expertise • Liaises with colleagues from other disciplines with the purpose of discussing project-related matters, sharing experiences and reporting progress • Ensures that work is performed in accordance with appropriate Safety, Health & Environment (SHE), quality and compliance standards, e.g. Good Laboratory Practice (GLP)
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees