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 help biotech and pharma customers save precious time and money in getting drugs to patients.
We employ more than 1,100 talented 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 community that’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 Role 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 a Formulation Scientist you 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 schedule
Prepare and characterise formulations
Work in a safe responsible manner at all times and towards the implementation of GLP and 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.
Write internal and external reports as necessary.
Communicate progress of in vitro and in vivo projects effectively to senior managers or Quotient staff as required
Carry out routine cleaning and general laboratory maintenance duties, as required
Be aware of the need for confidentiality outside the company
Perform other duties as reasonably required
The Candidate The 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.
Application Requirements
When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.
Our Commitment to Diversity, Equity and Inclusion
Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.
Specifically we will not 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 applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination. #J-18808-Ljbffr
We employ more than 1,100 talented 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 community that’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 Role 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 a Formulation Scientist you 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 schedule
Prepare and characterise formulations
Work in a safe responsible manner at all times and towards the implementation of GLP and 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.
Write internal and external reports as necessary.
Communicate progress of in vitro and in vivo projects effectively to senior managers or Quotient staff as required
Carry out routine cleaning and general laboratory maintenance duties, as required
Be aware of the need for confidentiality outside the company
Perform other duties as reasonably required
The Candidate The 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.
Application Requirements
When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.
Our Commitment to Diversity, Equity and Inclusion
Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.
Specifically we will not 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 applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination. #J-18808-Ljbffr
