Senior Formulation Scientist

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Quotient Sciences

To lead pre-clinical or stand-alone formulation programmes requiring specialist formulation knowledge including the preparation of associated protocols and reports
To design and conduct formulation development work including pre-formulation and formulation characterisation
To design the development and validation of radiolabelling methods for clinical studies
To support the transfer of formulation and radiolabelling methods into GMP clinical manufacturing, with input on manufacturing protocols, validation criteria and other key parameters
To write experimental protocol and reports

Lead pre-clinical formulation development programmes
To plan experiments and write protocols, according to an agreed work schedule
To prepare and characterise formulations
To perform radiolabelling method development, validation activities
Train new/existing staff as required
Work in a safe responsible manner at all times to GMP
Storage, use and disposal of Radioactive Isotopes in line with regulatory requirements and PP SOPs, to include liaising with Radiation Protection Supervisor (RPS) or nominated Deputy on any radiation protection issues that may arise.
Keeping detailed and accurate records of all work undertaken.
Accurate analysis and calculation of results, in line with written Protocol and/or SOPs of the company.
To communicate progress of in vitro and in vivo projects effectively to senior managers or Quotient staff as required
To be aware of the need for confidentiality outside the company
To perform other duties as reasonably required

To source and control formulation excipients
Provide formulation expertise to support other formulation scientists within the group

Very high concentration of work
Strict and tight deadlines
Having to juggle a range of tasks/issues simultaneously
Working in a hazardous environment with high requirement to follow safety procedures
Working outside normal working hours
Needing to respond to client demands

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