Formulation Scientist II
Quotient Sciences
Reading, United Kingdom
The Role
- To lead pre-clinical or stand-alone formulation programmes requiring specialist formulation knowledge;
- To design and conduct formulation development work including pre-formulation and formulation characterisation;
- To support the transfer of formulation development programs into GMP clinical manufacturing with input on manufacturing protocols, validation criteria and other key parameters;
- To write experimental protocols and reports.
Main Tasks And Responsibilities
- Lead pre-clinical formulation development programmes;
- To plan experiments and write protocols and reports, according to an agreed work schedule;
- Provide support on cross-site projects/technology transfer as required;
- Accurate analysis and calculation of results, in line with written Protocol and /or SOPs of the company;
- To prepare and characterise formulations;
- Train new/existing staff as required;
- Keeping detailed and accurate records of all work undertaken;
- 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;
- Work in a safe responsible manner at all times to GMP.
Additional Tasks/responsibilities
- Provide formulation expertise to support other formulation scientists within the group;
- To source and control formulation excipients.
Qualifications And Experience Required For Competent Performance
- Minimum degree level qualification in pharmacy or chemistry related discipline;
- >5 years’ experience in formulation development;
- cGMP experience will be at advantage.
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