Manufacturing Scientist

at  Quotient Sciences

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
We have an excellent career opportunity for a Manufacturing Scientist to join our team in Alnwick.
Depending on your knowledge and experience, you will primarily be responsible for dispense, manufacture and package of clinical products in accordance with GMP requirements and company procedures.

Main tasks and responsibilities

• As guided/requested, manufacture and package oral and intravenous clinical products.
• Prepare and complete documentation associated with the manufacture and supply of clinical products.
• Dispense APIs, excipients, drug products, IMPs, and packaging materials for clinical use and maintain GMP stocks as required.
• Participate in the cleaning, maintenance and upkeep of the GMP manufacturing facility, utilities and equipment.
• Record work in compliance with relevant regulatory requirements, internal policies/procedures and, where appropriate, client requirements.
• 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 and purchasing officer.
• 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 and knowledge of the drug development process is advantageous.
The successful candidate will have good written and oral communication skills and flexible approach to new work challenges.
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

• As guided/requested, manufacture and package oral and intravenous clinical products.
• Prepare and complete documentation associated with the manufacture and supply of clinical products.
• Dispense APIs, excipients, drug products, IMPs, and packaging materials for clinical use and maintain GMP stocks as required.
• Participate in the cleaning, maintenance and upkeep of the GMP manufacturing facility, utilities and equipment.
• Record work in compliance with relevant regulatory requirements, internal policies/procedures and, where appropriate, client requirements.
• 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 and purchasing officer.
• Work with due regards to health and safety of self and others.
• Work flexibly across the site to meet business needs