Quotient Sciences
GMP Manufacturing Scientist
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Arcinova, A Quotient Sciences Company
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.
The Role
We are looking for a GMP Manufacturing Scientist to support the manufacture, dispensing and packaging of clinical products within a regulated pharmaceutical manufacturing environment. This is an excellent opportunity for someone with a background in science who is looking to build their experience in GMP manufacturing, clinical supplies and pharmaceutical development.
Working as part of a skilled manufacturing team, you will help ensure clinical products are prepared to high quality standards, in line with GMP requirements, internal procedures and client expectations. This role would suit someone who is detail-focused, organised and comfortable working in a regulated environment where accuracy, safety and documentation are essential.
Key Responsibilities
- Manufacture, dispense and package oral and intravenous clinical products in accordance with GMP requirements and company procedures.
- Prepare and complete documentation relating to the manufacture and supply of clinical products.
- Dispense APIs, excipients, drug products, IMPs and packaging materials for clinical use.
- Maintain GMP stock levels, including supporting ordering, goods receipt, storage and stock control.
- Support the cleaning, maintenance and general upkeep of the GMP manufacturing facility, utilities and equipment.
- Record all work accurately and in line with regulatory requirements, internal policies, procedures and client requirements.
- Support process development studies and the manufacture of non-clinical batches where required.
- Work closely with Quality Control, microbiology teams and purchasing colleagues to support effective material management.
- Follow health and safety procedures at all times to protect yourself, colleagues and the wider working environment.
- Work flexibly across the site to support business and client needs.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Skills and Experience Required
Essential:
- BSc or equivalent qualification in a relevant scientific discipline.
- Good written and verbal communication skills.
- Strong attention to detail and the ability to follow procedures accurately.
- Ability to work in a regulated environment where documentation, quality and compliance are important.
- Organised approach with the ability to manage a range of tasks and priorities.
- Positive and flexible approach to new work challenges.
- Commitment to health, safety and GMP standards.
- Experience working in a GMP regulated facility or GMP manufacturing environment.
Desirable:
- Experience manufacturing clinical formulations or pharmaceutical products.
- Knowledge of the drug development process.
- Experience working with APIs, excipients, IMPs or clinical packaging materials.
- Experience supporting stock control, goods receipt or materials management within a regulated setting.
Learning Opportunities
This role offers the opportunity to develop practical experience in GMP pharmaceutical manufacturing and clinical product preparation. You will gain exposure to regulated processes, clinical formulation development, documentation standards, stock control and cross-functional working with Quality Control, microbiology and purchasing teams.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
You will also build your understanding of how clinical products are manufactured and supplied, supporting your development within pharmaceutical manufacturing, clinical supplies or GMP operations.
Eligibility to Work in the UK (if role is not eligible for visa sponsorship)
Please note that this position is not eligible for sponsorship under the UK points-based immigration system. If you require sponsorship, we will be unable to progress your application or make an offer of employment.
As this is a permanent role, we are also unable to accept applications from candidates on a Graduate Visa.
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.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills
Location