Production Chemist

Arcinova, A Quotient Sciences Company, is dedicated to providing innovative contract research, development, and manufacturing services. We offer a comprehensive range of integrated specialist services for early stage drug development, underpinned by strong industry knowledge and scientific expertise. Our mission is to bring science, innovation, and collaboration together to overcome the barriers in drug development. We empower emerging biotechs and large pharma alike to bring life-changing therapies to patients faster, through an efficient, effective approach focused on quality, science, and innovation.

Our vision is to advance progress through science, delivering solutions that make a measurable difference. We look ahead with purpose, driven to shape a smarter, more resilient future for all.

We are excited to welcome a Drug Substance Production Chemist to our Alnwick team. If you enjoy hands-on chemistry, thrive in a collaborative manufacturing environment, and want to play a key part in delivering high-quality GMP drug substance, this could be a fantastic next step for you.

In this role, you will support GMP manufacturing and scale-up activities across a 24-hour Monday–Friday shift pattern. You will be involved in batch synthesis, in-process testing, maintaining clear and accurate documentation, and working closely with colleagues in QC and across the wider site. It is a great opportunity to grow your experience within a supportive team and a fast-paced, science-driven environment.

• Carry out drug substance manufacturing and scale-up operations in accordance with regulatory and company procedures, including shift working as required.
• Perform in-process analysis, including sample preparation, interpretation of results, and usage testing of critical raw materials and intermediates.
• Operate within Environmental, Health and Safety guidelines and regulations.
• Maintain equipment usage logs, calibration records, and Laboratory Notebooks.
• Liaise with the QC team to ensure in-process analyses are completed in line with the production plan.
• Review completed Batch Synthesis Instructions and other process documentation.
• Contribute to the preparation of quality documentation, including changes, unplanned deviations, and corrective actions.
• Support EHS risk assessments and CoSHH assessments.
• Participate in process risk assessments and continuous improvement activities.
• Contribute to raw material and equipment acquisition, maintenance, installation, and validation as required.
• Carry out sampling and booking-in of materials into the Materials Management System and maintain effective stock control for manufacturing activities.
• Maintain a high standard of housekeeping and manage waste disposal, liaising with relevant departments as required.
• Ensure that manufacturing and scale-up operations, and all associated documentation, comply with GMP, regulatory requirements, internal procedures, and client expectations.
• Work with due regard to the health and safety of yourself and others.
• Work flexibly across the site to meet business needs.

• A degree (or equivalent) in Chemistry or a closely related discipline, or a completed apprenticeship as a chemical operator.
• A strong interest in practical chemistry and manufacturing processes.
• Good attention to detail and a proactive approach to documentation and compliance.
• Willingness to work a shift pattern within a GMP environment.

• Experience in GMP, pharmaceutical, or chemical manufacturing.
• Previous experience working in a shift-based role.
• Familiarity with batch manufacturing, scale-up operations, or in-process analytical techniques.

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.

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,…