Posted Thursday 13 November 2025 at 06:00
Quotient Sciences: Molecule to Cure. Fast.
We accelerate drug development by integrating formulation development, clinical testing, data sciences, and manufacturing into one seamless process. Our proprietary platform, Translational Pharmaceutics®, shortens timelines by 9–12 months on average.
Arcinova, our specialist arm in Reading and Alnwick, UK, delivers end-to-end drug substance and early drug product services, including bioanalysis and radiolabeling—streamlining early development from candidate selection to proof of concept.
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.
Summary of Job Purpose
To provide QA support to operations functions at the QS Alnwick site and assist in maintaining the site Quality Management System (QMS), ensuring compliance with GxP guidelines and regulatory requirements.
Key Responsibilities
* Prepare, review and approve quality documents including batch manufacturing records and study reports.
* Act as QA representative for Quality Events and serve as RCA coach.
* Provide support for the use of the electronic Quality Management System (eQMS).
* Assist in the preparation and review of Quality Agreements.
* Participate in the Supplier Qualification programme.
* Assist in the conduct of site audits, including:
* Facility-based audits
* GxP process-based audits
* Study data and report reviews
* Support customer audits and regulatory inspections, including completion of questionnaires, coordination of responses and follow-up of corrective actions.
* Ensure compliance with GxP guidelines and regulations as required by the role.
Qualifications & Experience
* Educated to degree level (or equivalent) in a relevant scientific discipline.
* 1–2 years’ experience in a GMP Quality role (QA/QC).
Key Skills
* Strong interpersonal and communication skills, both written and oral.
* Self-motivated with the ability to work independently and as part of a team.
* Excellent attention to detail and organisational skills.
* High level of personal integrity and commitment.
* 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.
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