Manufacturing Scientist in Alnwick

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.

The Role

Our Drug Product Manufacturing team in Alnwick plays a vital role in producing small-scale batches of oral and intravenous products for global clinical trials. We’re looking for a Manufacturing Scientist who is passionate about science, thrives in a GMP-regulated environment, and wants to contribute to life-changing research.

Main Tasks and Responsibilities

• Manufacturing, packaging, and labelling a variety of dosage forms—including oral and intravenous—for use in clinical trials.
• Dispensing APIs, excipients, drug products, IMPs, and packaging materials for clinical use, while maintaining GMP stock levels as required.
• Preparing and completing documentation related to the manufacture and supply of clinical products, ensuring accuracy and compliance.
• Recording all work in line with regulatory requirements, internal procedures, and client specifications where applicable.
• Supporting the cleaning, maintenance, and upkeep of the GMP manufacturing facility, utilities, and equipment.
• Assisting with process development studies and the manufacture of non-clinical batches to support formulation development or GMP transfer.
• Managing GMP material inventory, including ordering, goods receipt, storage, and stock control, in collaboration with Quality Control and microbiology teams.
• Working safely and responsibly, with due regard for the health and safety of yourself and others.
• Adapting to business needs, working flexibly across the site as required.

The Candidate

We’re looking for someone who is proactive, detail-oriented, and ready to grow. Ideally, you will have:

• ABSc (Hons) or equivalent in a relevant scientific subject, and/or at least 1 year of experience working within pharmaceutical manufacturing teams.
• Experience with, or an understanding of, aseptic manufacturing is a bonus.
• Good written and oral communication skills, with the ability to work effectively in a team.
• A diligent, detail-oriented approach to work.
• Flexible and adaptable, including a willingness to work outside normal hours if required.
• A self-starter who takes ownership and sees tasks through to completion.

What we can offer

• Share your expertise – With your knowledge and experience, this is your chance to share your knowledge and contribute to the continuous improvement of the team.
• Develop hands-on experience – You will develop your skills within the Drug Product manufacturing from aseptic manufacture to oral solid dose over a range of projects.
• Industry - This is a fantastic opportunity for you to develop your skills in Phase I manufacturing processes while working in a state-of-the-art facility.
• Career growth – As we evolve, you will have excellent opportunities to progress and advance your career.

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.