Quotient Sciences
Nottingham, Nottinghamshire
Quotient Sciences: Molecule to Cure. Fast. Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing. Our proprietary and disruptive platform - "Translational Pharmaceutics " - integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improve outcomes, and significantly accelerates drug development times. Why Join Us Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact-fast. 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. 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. Our Approach to AI in Recruitment At Quotient Sciences, we use technology, including AI-enabled tools, to support parts of our recruitment process and help create an efficient, consistent, and inclusive candidate experience. Any use of AI is subject to human oversight, and hiring decisions are made by people, not technology. While we embrace innovation, our recruitment process remains deeply human. Candidates who progress through our recruitment process are supported by a dedicated recruitment contact, and many of our selection processes include in person interviews. We believe the best hiring decisions come from real conversations, giving candidates the opportunity to meet future colleagues, experience our culture and showcase their strengths beyond their application. We recognize that candidates may choose to use AI tools when preparing applications. We encourage the responsible use of technology to support research, preparation, and drafting. However, applications should reflect your own skills, experiences, and perspectives. Throughout the recruitment process, we assess authenticity, critical thinking, technical capability, and the unique contribution you can bring to Quotient Sciences. Content generated entirely by AI may not provide an accurate representation of your suitability for the role.
Quotient Sciences: Molecule to Cure. Fast. Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing. Our proprietary and disruptive platform - "Translational Pharmaceutics " - integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improve outcomes, and significantly accelerates drug development times. Why Join Us Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact-fast. 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. 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. Our Approach to AI in Recruitment At Quotient Sciences, we use technology, including AI-enabled tools, to support parts of our recruitment process and help create an efficient, consistent, and inclusive candidate experience. Any use of AI is subject to human oversight, and hiring decisions are made by people, not technology. While we embrace innovation, our recruitment process remains deeply human. Candidates who progress through our recruitment process are supported by a dedicated recruitment contact, and many of our selection processes include in person interviews. We believe the best hiring decisions come from real conversations, giving candidates the opportunity to meet future colleagues, experience our culture and showcase their strengths beyond their application. We recognize that candidates may choose to use AI tools when preparing applications. We encourage the responsible use of technology to support research, preparation, and drafting. However, applications should reflect your own skills, experiences, and perspectives. Throughout the recruitment process, we assess authenticity, critical thinking, technical capability, and the unique contribution you can bring to Quotient Sciences. Content generated entirely by AI may not provide an accurate representation of your suitability for the role.
Quotient Sciences
Alnwick, Northumberland
The Role We are looking for anAseptic Manufacturing Scientist to join our GMP manufacturing team, supporting the manufacture, dispensing and packaging of clinical products within a regulated pharmaceutical environment. This is an excellent opportunity for someone with a scientific background who is looking to build experience in aseptic manufacturing, clinical supplies and pharmaceutical development. Working as part of a skilled manufacturing team, you will help ensure clinical products are prepared to high quality standards, in line with GMP requirements, internal procedures and client expectations. This role would suit someone who is detail-focused, organised and comfortable working in a regulated environment where accuracy, safety and documentation are essential. Key responsibilities Manufacture, dispense and package oral and intravenous clinical products in accordance with GMP requirements and company procedures. Prepare and complete documentation relating to the manufacture and supply of clinical products. Dispense APIs, excipients, drug products, IMPs and packaging materials for clinical use. Maintain GMP stock levels, including supporting ordering, goods receipt, storage and stock control. Support the cleaning, maintenance and general upkeep of the GMP manufacturing facility, utilities and equipment. Record all work accurately and in line with regulatory requirements, internal policies, procedures and client requirements. Support process development studies and the manufacture of non-clinical batches where required. Work closely with Quality Control, microbiology teams and purchasing colleagues to support effective material management. Follow health and safety procedures at all times to protect yourself, colleagues and the wider working environment. Work flexibly across the site to support business and client needs. Skills and experience required Essential: BSc or equivalent qualification in a relevant scientific discipline. Good written and verbal communication skills. Strong attention to detail and the ability to follow procedures accurately. Ability to work in a regulated environment where documentation, quality and compliance are important. Organised approach with the ability to manage a range of tasks and priorities. Positive and flexible approach to new work challenges. Commitment to health, safety and GMP standards. Experience working in a GMP regulated facility or GMP manufacturing environment. Desirable: Experience manufacturing clinical formulations or pharmaceutical products. Knowledge of the drug development process. Experience working with APIs, excipients, IMPs or clinical packaging materials. Experience supporting stock control, goods receipt or materials management within a regulated setting. Eligibility to Work in the UK Please note that this position isnot eligible for sponsorship under the UK points-based immigration system. If you require sponsorship, we will be unable to progress your application or make an offer of employment. As this is apermanent role, we are also unable to accept applications from candidates on a Graduate Visa.
The Role We are looking for anAseptic Manufacturing Scientist to join our GMP manufacturing team, supporting the manufacture, dispensing and packaging of clinical products within a regulated pharmaceutical environment. This is an excellent opportunity for someone with a scientific background who is looking to build experience in aseptic manufacturing, clinical supplies and pharmaceutical development. Working as part of a skilled manufacturing team, you will help ensure clinical products are prepared to high quality standards, in line with GMP requirements, internal procedures and client expectations. This role would suit someone who is detail-focused, organised and comfortable working in a regulated environment where accuracy, safety and documentation are essential. Key responsibilities Manufacture, dispense and package oral and intravenous clinical products in accordance with GMP requirements and company procedures. Prepare and complete documentation relating to the manufacture and supply of clinical products. Dispense APIs, excipients, drug products, IMPs and packaging materials for clinical use. Maintain GMP stock levels, including supporting ordering, goods receipt, storage and stock control. Support the cleaning, maintenance and general upkeep of the GMP manufacturing facility, utilities and equipment. Record all work accurately and in line with regulatory requirements, internal policies, procedures and client requirements. Support process development studies and the manufacture of non-clinical batches where required. Work closely with Quality Control, microbiology teams and purchasing colleagues to support effective material management. Follow health and safety procedures at all times to protect yourself, colleagues and the wider working environment. Work flexibly across the site to support business and client needs. Skills and experience required Essential: BSc or equivalent qualification in a relevant scientific discipline. Good written and verbal communication skills. Strong attention to detail and the ability to follow procedures accurately. Ability to work in a regulated environment where documentation, quality and compliance are important. Organised approach with the ability to manage a range of tasks and priorities. Positive and flexible approach to new work challenges. Commitment to health, safety and GMP standards. Experience working in a GMP regulated facility or GMP manufacturing environment. Desirable: Experience manufacturing clinical formulations or pharmaceutical products. Knowledge of the drug development process. Experience working with APIs, excipients, IMPs or clinical packaging materials. Experience supporting stock control, goods receipt or materials management within a regulated setting. Eligibility to Work in the UK Please note that this position isnot eligible for sponsorship under the UK points-based immigration system. If you require sponsorship, we will be unable to progress your application or make an offer of employment. As this is apermanent role, we are also unable to accept applications from candidates on a Graduate Visa.