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For Companies At a Glance
- Tasks: Join our team to manufacture innovative medicines and support clinical trials.
- Company: Quotient Sciences accelerates drug development with a culture of science and agility.
- Benefits: Enjoy a dynamic work environment with opportunities for growth and learning.
- Why this job: Make a real impact in healthcare by bringing new medicines to patients faster.
- Qualifications: Some experience in GMP/GLP, strong communication skills, and attention to detail required.
- Other info: Must be 18+ to apply; we value diversity and inclusion in our workforce.
The predicted salary is between 24000 - 36000 £ per year.
Join to apply for the Manufacturing Operator role at Quotient Sciences.
Quotient Sciences: Molecule to Cure. Fast. We accelerate drug development by integrating formulation development, clinical testing, data sciences, and manufacturing into one seamless process. Our proprietary platform, Translational Pharmaceutics, shortens timelines by 9–12 months on average.
Arcinova, our specialist arm in Reading and Alnwick, UK, delivers end-to-end drug substance and early drug product services, including bioanalysis and radiolabeling—streamlining early development from candidate selection to proof of concept.
Why join us? Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact—fast.
The Role
We are looking for a Manufacturing Operator to join our Clinical Manufacturing team in Reading. This is a hands-on role where you’ll be responsible for manufacturing Investigational Medicinal Products (IMPs) including capsules, tablets, liquids, creams, gels, and inhalation dosage forms. You’ll also support the transfer of processes from development into clinical trial manufacturing and help maintain our GMP cleanroom facilities.
Main Tasks And Responsibilities
- Manufacture pharmaceuticals to Good Manufacturing Practice (GMP) standards and internal Standard Operating Procedures (SOP), while adhering to Good Documentation Practice (GDocP).
- Direct involvement in tasks associated with the running and maintenance of the GMP cleanroom, including room set-up for manufacturing activities and cleaning of required equipment and consumables.
- Complete weekly workloads based on the schedule of Clinical Manufacturing and Development activities provided by the Head of Production (HOP) or nominated deputy.
- Preparation of working BMRs, checked working labels, processing rooms, equipment, consumables, cleaning documents, swabbing procedures, and COSHH (as appropriate) prior to onset of manufacturing operations.
- Ensure manufacturing/validation procedures are carried out as per approved protocols in a reproducible manner with minimal avoidable errors. Adhere to KPI targets set by the Head of Department.
- Work in a safe and responsible manner at all times.
- Communicate progress of development and clinical trial manufacturing projects effectively to the Head of Production (HOP), QA, and Project Management teams to support realistic goal setting and timely client updates.
- Direct involvement in specific continuous improvement activities and highlight any improvements needed for equipment, storage, and processes.
Qualifications And Experience Required
- Some work experience (GMP/GLP) in similar type of work
- Excellent interpersonal and communication skills
- Excellent organizational, problem-solving, and follow-up skills
- Ability to perform multiple tasks and prioritize effectively
- Excellent attention to detail
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.
Seniority level
- Entry level
Employment type
- Full-time
Job function
- Management and Manufacturing
Industries
- Pharmaceutical Manufacturing
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Manufacturing Operator employer: Quotient Sciences
Contact Detail:
Quotient Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Manufacturing Operator
✨Tip Number 1
Familiarise yourself with Good Manufacturing Practice (GMP) standards and internal Standard Operating Procedures (SOP). Understanding these guidelines will not only help you in the role but also demonstrate your commitment to quality and safety during the interview process.
✨Tip Number 2
Highlight any previous experience you have in a GMP or GLP environment. Even if it's limited, showcasing your understanding of these practices can set you apart from other candidates.
✨Tip Number 3
Prepare to discuss specific examples of how you've effectively communicated progress on projects in past roles. This will show your potential employer that you can work collaboratively and keep teams informed, which is crucial in a fast-paced manufacturing environment.
✨Tip Number 4
Research Quotient Sciences and their approach to drug development. Being knowledgeable about their processes and values will allow you to tailor your responses during interviews and demonstrate your genuine interest in joining their team.
We think you need these skills to ace Manufacturing Operator
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Manufacturing Operator position. Understand the key responsibilities and qualifications required, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous experience you have in GMP or GLP environments. Be specific about your roles and how they relate to the tasks mentioned in the job description.
Showcase Your Skills: Make sure to highlight your interpersonal, organisational, and problem-solving skills in your application. Provide examples of how you've successfully managed multiple tasks or improved processes in past roles.
Tailor Your Application: Customise your CV and cover letter to reflect Quotient Sciences' values and commitment to diversity, equity, and inclusion. Mention how you can contribute to their culture and goals, particularly in the context of drug development.
How to prepare for a job interview at Quotient Sciences
✨Understand GMP Standards
Familiarise yourself with Good Manufacturing Practice (GMP) standards and how they apply to the role. Be prepared to discuss your understanding of these regulations and any relevant experience you have in adhering to them.
✨Showcase Your Attention to Detail
As a Manufacturing Operator, attention to detail is crucial. Prepare examples from your past work where your meticulousness led to successful outcomes, especially in a manufacturing or laboratory setting.
✨Communicate Effectively
Effective communication is key in this role. Think of instances where you successfully communicated progress or issues in a team environment. Be ready to demonstrate how you can keep stakeholders informed.
✨Highlight Problem-Solving Skills
Manufacturing often involves unexpected challenges. Prepare to discuss specific problems you've encountered in previous roles and how you resolved them, particularly in a GMP or cleanroom environment.