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.
The Role
As a QA Associate, you'll play a key role in supporting operational functions and maintaining our site's Quality Management System. You'll work across departments to uphold GxP standards and contribute to the delivery of safe, effective medicines.
Key Responsibilities
* Prepare, review, and approve quality documentation including batch manufacturing records and study reports.
* Act as QA representative for quality events and provide RCA coaching.
* Support the use and maintenance of the electronic Quality Management System (eQMS).
* Assist in the preparation and review of Quality Agreements.
* Participate in the Supplier Qualification programme.
* Conduct and support site audits including facility, GxP process, and study data audits.
* Provide support during customer audits and regulatory inspections, including coordination of responses and follow-up actions.
* Ensure full compliance with GxP guidelines and regulatory requirements.
About You
* Degree (or equivalent) in a relevant scientific discipline.
* 1–2 years' experience in a GMP Quality role (QA or QC).
* Strong interpersonal and communication skills—both written and verbal.
* Self-motivated with the ability to work independently and collaboratively.
* High attention to detail and a flexible approach to new challenges.
* Demonstrates integrity, commitment, and a proactive mindset.
Why Quotient?
We offer a dynamic and supportive environment where your contributions make a real impact. At Quotient Sciences, you'll be part of a team that values innovation, collaboration, and continuous improvement.
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.