QA Lead

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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.

About The Role

At Arcinova, we are committed to accelerating the development and manufacture of life-changing medicines. As a QA Lead, you will play a pivotal role in ensuring our quality systems and processes meet the highest regulatory standards while supporting operational excellence across the site.

This is a key leadership position within the Quality Assurance team, where you will oversee compliance activities, mentor QA professionals, and collaborate cross-functionally to uphold our commitment to quality and continuous improvement.

Key Responsibilities

• Lead and manage QA activities to ensure compliance with GxP regulations and Arcinova’s quality standards.
• Oversee the review and approval of quality documentation, including deviations, CAPAs, change controls, and validation records.
• Support internal and external audits, including regulatory inspections and client audits.
• Drive continuous improvement initiatives within the QA function and across operational teams.
• Provide guidance and training to QA staff and other departments on quality systems and regulatory expectations.
• Collaborate with cross-functional teams to ensure timely resolution of quality issues.
• Maintain up-to-date knowledge of industry regulations and best practices.

What We’re Looking For

• A degree in Life Sciences or a related discipline.
• Significant experience in a QA role within a GxP-regulated environment (GLP, GCP, or GMP).
• Strong understanding of quality systems, regulatory compliance, and industry standards.
• Proven leadership and team management experience.
• Excellent communication, decision-making, and problem-solving skills.
• Ability to work collaboratively across departments and with external stakeholders.
• Proficiency in Microsoft Office and electronic quality systems.

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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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