Analytical Operations Associate

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
As an Analytical Reviewer, you will play a key role in ensuring data integrity and compliance within our Quality Control function. You will review analytical data, documentation, and raw data (including Empower and ELN) to ensure adherence to GMP standards. Your responsibilities will include authoring and reviewing analytical documentation, supporting raw material release, external testing, and stability activities, as well as archiving analytical records.

This role will be 3 days per week 22.5 hours
Key Responsibilities

• Review laboratory data packages, notebooks, ELN entries, Waters Empower outputs, and spreadsheets for GMP compliance.
• Verify data integrity in line with ALCOA+ principles and internal SOPs.
• Communicate effectively with analysts to ensure timely sign-off and meet cycle time targets.
• Support generation of QC documentation (protocols, reports, COAs, specifications).
• Assist with raw material release, external testing coordination, and stability pulls/set-downs.
• Archive analytical documentation as required.

Qualifications & Experience

• Minimum HND/HNC or equivalent in a laboratory-focused discipline.
• At least 3 years' experience in Pharmaceutical Analytical Chemistry.
• Strong understanding of cGMP and ALCOA+ principles.
• Familiarity with routine analytical techniques and data used in pharmaceutical industries.
• Excellent attention to detail, documentation skills, and interpersonal communication.
• Preferably some experience with Waters Empower systems.

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.