Formulation Scientist

Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we helpbiotech and pharma customers save precious time and money in getting drugs to patients.
As a growing and successful business, we employ more than 1,300talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA.
Science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it. People join Quotient Sciences because we are a respected member of the drug development communitythat’s focused on innovation and are driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures,
fast. Because humanity needs solutions, fast. The RoleDue to business growth, we have an exciting career opportunity available for a Formulation Scientist at our site in Nottingham.Quotient Sciences’ formulation teams have vast experience across an array of drug product formats for administration via; solid oral dosage forms, oral and nasal dosage forms, solubility-enhanced dosage forms, parenterals, gels, ointments and creams.As aFormulation Scientistyou will conduct formulation development work including pre-formulation and formulation characterisation whilst supporting development and validation of radiolabelling methods for clinical studies. You’ll transfer formulation and radiolabelling methods into GMP clinical manufacturing, with input on manufacturing protocols, validation criteria and other key parameters and write experimental protocol and reports.Main tasks and responsibilities:Plan experiments and write protocols, according to an agreed work schedulePrepare and characterise formulationsWork in a safe responsible manner at all times and towards the implementation of GLP and GMPStorage, 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.Write internal and external reports as necessary.Communicate progress ofin vitroandin vivoprojects effectively to senior managers or Quotient staff as requiredCarry out routine cleaning and general laboratory maintenance duties, as requiredBe aware of the need for confidentiality outside the companyPerform other duties as reasonably requiredThe CandidateThe successful candidate will have a degree level science qualification in pharmaceutical sciences or related discipline. Previous formulation development experience within the pharmaceutical industry is required for this role.Other skills and experience required:GMP experience will be an advantageAbility to work to tight deadlines, whilst juggling a range of tasks simultaneouslyGood interpersonal and communication skillsHigh attention to detailKnowledge on pediatric product development would be desirable
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We are an Equal Employment Opportunity (“EEO”) Employer.
It has been and will continue to be a fundamental policy of Quotient Sciences not to discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.
This policy applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
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