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Our Commitment to Science and Collaboration
Arcinova, a Quotient Sciences Company, delivers innovative contract research, development, and manufacturing services. We combine early-stage drug development expertise, regulatory knowledge, and scientific innovation to tackle the challenges of biopharmaceutical discovery.
Our mission is to accelerate life-changing therapies for patients by fostering collaboration, efficiency, and scientific precision. Together with our partners, we strive to build a resilient future where healthcare advances are both measurable and meaningful.
The Role: Bioanalyst (Alnwick Site)
We are recruiting a dedicated Bioanalyst to join our Bioanalytical Services team at our onsite Alnwick location. Reporting directly to a Bioanalytical Study Director, this role focuses on delivering high-quality bioanalytical support across preclinical and clinical assays.
Key Responsibilities
Sample Analysis and Validation
- Conduct ICP-MS and LC-MS bioanalytical assays on samples from preclinical and clinical studies
- Perform method validation to ensure regulatory compliance and data integrity
- Develop and implement new assay methodologies to support investigational research
Quality Assurance and Compliance
- Ensure all work adheres to regulatory requirements, internal policies, and client specifications
- Regularly review and update supporting documentation, including SOPs and data reports
- Maintain strict quality standards throughout all bioanalytical operations
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Collaboration and Problem-Solving
- Work closely with study teams to resolve technical challenges and optimise study execution
- Critically analyse data, acting as a key resource for study-related discussions
Skills and Experience Required
Essential
✅ BSc (Hons) in a relevant scientific discipline (e.g., chemistry, pharmacy, biochemistry), or equivalent lab experience ✅ Ability to critically assess and interpret scientific data ✅ Strong written and verbal communication skills for technical reporting and stakeholder updates ✅ Self-motivated, adaptable, and proactive in tackling new challenges ✅ High level of personal integrity and unwavering attention to quality and compliance
Desirable (Preferred Qualifications)
✔ Previous experience with mass spectrometry (specifically ICP-MS or LC-MS) ✔ Experience within pharmaceutical, contract research organisations (CROs), or regulated laboratory environments ✔ Familiarity with GxP standards, FDA, or EMA guidelines for bioanalytical work
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Eligibility Requirements
Work Authorization
- Mandatory eligibility to work in the UK – roles under Quotient Sciences do not qualify for sponsorship under the UK points-based system ⚠️ Applicants on a Graduate Visa or under 18 will be unable to proceed with their application.
Compliance
- Applicants must be aged 18+ and not debarred by the FDA—failure to disclose relevant information will result in automatic rejection of your application.
Our Diversity, Equity, and Inclusion Commitment
At Quotient Sciences, we are dedicated to fostering an inclusive workplace culture that celebrates difference and empowers every team member. We are firmly committed to equality, ensuring no discrimination based on:
- Race, colour, creed, or religion
- Gender, gender identity, pregnancy, or marital/partnership status
- Sexual orientation, age, national origin, military status, or disability
- Medical condition, caregiver status, unemployment status, or any characteristic protected by regulation
This principle applies transparently across hiring, promotion, training, working conditions, and benefits. We actively seek diverse perspectives to shape the future of our globally distributed teams and advance our scientific mission together.
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