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 are recruiting Manufacturing Scientists at our Alnwick site, Northumberland.
The Drug Product Manufacturing team at Alnwick manufacture small scale batches of oral and intravenous clinical products for clinical trials on behalf of our global clients.
With your knowledge and experience, this is your chance to contribute to the continuous improvement of the team and a fantastic opportunity for someone looking to take on a critical role while contributing to life-changing clinical research.

Main tasks and responsibilities

• Participate in the manufacture, packaging and labelling of various dosage forms such as oral/intravenous for clinical trials.
• Dispense APIs, excipients, drug products, IMPs, and packaging materials for clinical use and maintain GMP stocks as required.
• Prepare and complete documentation associated with the manufacture and supply of clinical products.
• Record work in compliance with relevant regulatory requirements, internal policies/procedures and, where appropriate, client requirements.
• Participate in the cleaning, maintenance and upkeep of the GMP manufacturing facility, utilities and equipment.
• As guided/requested, participate in process development studies or the manufacture of non-clinical batches to assist in the development of clinical formulations or the transfer of clinical formulations into the GMP facility.
• Participate in the upkeep of the GMP material inventory including ordering, goods receipt, storage and stock control, liaising as appropriate with the Quality Control and microbiology teams.
• Work with due regards to health and safety of self and others.
• Work flexibly across the site to meet business needs.

The Candidate

• The ideal candidate will ideally have a BSc or equivalent in a relevant scientific discipline.
• Experience in the manufacturing of clinical formulations and working in a GMP regulated facility/manner.
• A background in drug product or drug substance manufacturing.
• Experience in small batch production for clinical trials
• Will be able to troubleshoot formulation and manufacturing challenges
• You will have good written and oral communication skills and flexible approach to new work challenges.
• Aseptic manufacturing experience and knowledge of the drug development process is advantageous.

What we can offer

• Share your expertise – With your knowledge and experience, this is your chance to share your knowledge and contribute to the continuous improvement of the team.
• Develop hands on experience – You will develop your skills within the Drug Product manufacturing from aseptic manufacture to oral solid dose over a range of projects.
• Industry - This is a fantastic opportunity for you to develop your skills in Phase I manufacturing processes while working in a state-of-the-art facility
• Career growth – As we evolve, you will have excellent opportunities to progress and advance your career

About Alnwick?

• Alnwick is a short drive from Newcastle, around 30 minutes. Many of our colleagues have relocated from other parts of the UK to the Newcastle area which is a vibrant city with plenty to do. The Northeast is named as one of the most affordable places to buy a house in the UK.
• Alnwick is located in the heart of Northumberland and is a town surrounded by beautiful countryside and coastline. Ideal for outdoor enthusiasts or those who appreciate nature.
• Alnwick is a historic town, full of culture and is known for its impressive heritage including the famous Alnwick Castle and Alnwick gardens.

Application Requirements
When applying for a position with Quotient Sciences to be able to work in our organisation 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 organisation. As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today.
Specifically we will not discriminate on the basis of race, colour, 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

• Participate in the manufacture, packaging and labelling of various dosage forms such as oral/intravenous for clinical trials.
• Dispense APIs, excipients, drug products, IMPs, and packaging materials for clinical use and maintain GMP stocks as required.
• Prepare and complete documentation associated with the manufacture and supply of clinical products.
• Record work in compliance with relevant regulatory requirements, internal policies/procedures and, where appropriate, client requirements.
• Participate in the cleaning, maintenance and upkeep of the GMP manufacturing facility, utilities and equipment.
• As guided/requested, participate in process development studies or the manufacture of non-clinical batches to assist in the development of clinical formulations or the transfer of clinical formulations into the GMP facility.
• Participate in the upkeep of the GMP material inventory including ordering, goods receipt, storage and stock control, liaising as appropriate with the Quality Control and microbiology teams.
• Work with due regards to health and safety of self and others.
• Work flexibly across the site to meet business needs