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Open nowPosted 39 days ago

Formulation Scientist (12-Month Fixed-Term Role)

quotientsci25 open roles

Where
Nottingham, UK
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Your applicationOpen nowFormulation Scientist (12-Month Fixed-Term Role)quotientsci · Nottingham, UK

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This job: posted 39 days ago

The posting

  The Role   We are looking for a Formulation Scientist to join our Formulation team at our Nottingham site on a 12-month fixed-term contract.   In this role, you will conduct formulation development activities, including pre-formulation studies and formulation characterisation, supporting the progression of projects from development through to GMP clinical manufacturing.   You will also be responsible for transferring formulation and radiolabelling methods into GMP manufacturing environments, contributing to manufacturing protocols, validation criteria, and other key project deliverables.   The successful candidate will prepare experimental protocols and reports while ensuring all work is performed in compliance with GxP regulations and Good Manufacturing Practice (GMP) standards.   Main tasks and responsibilities   

To plan experiments and write protocols, according to an agreed work schedule To prepare and characterise formulations To perform radiolabelling method development, validation activities Working in a safe responsible manner at all times to the principles of 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 write internal and external reports as necessary. To communicate progress of in vitro and in vivo projects effectively to senior managers or Quotient staff as required To carry out routine cleaning and general laboratory maintenance duties, as required To be aware of the need for confidentiality outside the company To perform other duties as reasonably required

  Additional tasks and responsibilities  

To source and control formulation excipients To book-in In-vitro raw materials for formulation development to the MMD database

  Qualifications and Experience Required 

Minimum degree-level qualification in a Pharmacy, Chemistry, or related discipline. Relevant work experience in formulation development and knowledge of radioisotopes would be desirable, but not essential. cGMP experience would be an advantage.

       

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