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- Tasks: Support GMP production of cutting-edge cell and gene therapies in a dynamic environment.
- Company: Join eXmoor Pharma, a leader in cell and gene therapy with 20 years of expertise.
- Benefits: Gain hands-on experience, develop your career, and work with a globally recognised team.
- Why this job: Make a real impact in the biotech field while learning from industry experts.
- Qualifications: BSc in Life Science or equivalent experience; GMP knowledge is a plus.
- Other info: Exciting growth opportunities in a rapidly expanding sector.
The predicted salary is between 36000 - 60000 £ per year.
eXmoor Pharma is the only integrated cell and gene therapy CDMO with over 20 years of consultancy expertise embedded across every stage of the CMC journey — from early-phase strategy to process development, GMP manufacturing and commercialisation. We provide comprehensive support across Viral Vectors, Autologous and Allogeneic Cell Therapies, and RNA technologies. This integrated model enables seamless progression from early-phase strategy through to commercial readiness.
The GMP Production Scientists will support the routine operation of eXmoor’s GMP production suites for a varied range of ATMP clinical products. This is an exciting opportunity to work with eXmoor’s globally recognised team of scientists, consultants and engineers. You will work on a wide range of Client projects in a rapidly growing business whilst developing your GMP manufacturing career.
Job Purpose: The GMP manufacturing facility will be capable of handling a wide range of cell and gene therapies as well as small scale complex biologics. The eXmoor facility will comprise of two technical areas Process/Analytical Development & GMP clinical phase production, including a small fill/finish capability and all associated QC, all working closely together such that processes developed in the PD/AD area will be transferred at scale to the GMP suites.
Main areas of responsibility / key duties:
- Production Processes: You will assist with the tech transfer & scale-up work within the GMP facility under GMP conditions and provide data for application to the regulatory authorities. You will carry out routine duties involved in the GMP manufacture of clinical grade ATMP products including closed processing cell culture, downstream purification and fill/finish at varying scales up to 200L. You will work with procurement to ensure GMP approved materials are available and support procurement to ensure delivery of the required materials. You will ensure that work in progress and finished products are produced, labelled and stored according to product specification and quality standards. You will assist with the development of production methods including closed processing cell culture, downstream purification and fill/finish at varying scales up to 200L.
- Production Facility: You will assist with the maintenance, operation, cleaning and validation of the Production Equipment in compliance with facility’s stated procedures and standards. You will assist with appropriate qualification, process validation and regular re-validations. You will assist in the monitoring and control of the production environment and ensure that standards of cleanliness and hygiene are maintained.
- Documentation: You will support the development and generation of SOPs & Batch Documentation relating to specific GMP facility and specific manufacturing operations.
- Safety: You will conduct your duties to the highest quality standard and in a safe way complying with all policies and procedures and with due care and attention for yourself and your peers. You will comply with GMP and Lab documentation including Risk assessments, SOPs, COSHH forms, lab notebooks and records.
Person Specification:
Essential Qualifications & Experience:
- BSc in Life Science or equivalent experience
- Operating within a GMP Quality system including the management of production deviations, change controls and the principle of quality risk management.
- Understanding or experience of one or more of the following unit operations: mammalian cell culture (adherent &/or suspension, up to 200L scale), autologous and allogeneic C>, purification of vectors, plasmids, whole cells, aseptic filling
- Resilience and flexibility; able to contribute innovatively to solving processing problems.
Desirable Qualifications & Experience:
- Additional work experience in a relevant field
Competences Required:
- Organisation, planning and time management
- Oral and written communication skills
- Teamworking
- Innovation, inquisitiveness, and willingness to learn
- Attention to detail and getting things finished
- Problem solving
- Building constructive relationships and earning respect
- Motivated by growing a bio-technology business in the CGT / biopharmaceutical market
- Proficiency in Office365 (including Word, Excel, PowerPoint).
GMP Production Scientist in Bristol employer: eXmoor Pharma Concepts Limited
Contact Detail:
eXmoor Pharma Concepts Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land GMP Production Scientist in Bristol
✨Tip Number 1
Network like a pro! Reach out to professionals in the GMP and biopharmaceutical fields on LinkedIn. Join relevant groups, participate in discussions, and don’t hesitate to ask for informational interviews. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for those interviews! Research eXmoor Pharma thoroughly—know their projects, values, and recent news. Practice common interview questions related to GMP production and be ready to discuss your experience with cell culture and purification processes.
✨Tip Number 3
Showcase your skills! Bring along a portfolio or a summary of your relevant projects and experiences to the interview. Highlight your understanding of GMP quality systems and any innovative solutions you've contributed to in past roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search. Let’s get you on board with the eXmoor team!
We think you need these skills to ace GMP Production Scientist in Bristol
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the GMP Production Scientist role. Highlight relevant experience in GMP environments and any specific skills that match the job description. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about cell and gene therapy and how your skills can contribute to our team at eXmoor Pharma. Keep it concise but impactful – we love a good story!
Showcase Your Attention to Detail: In the world of GMP, attention to detail is key. Make sure your application is free from typos and errors. This reflects your commitment to quality, which is super important in our field. We appreciate candidates who take pride in their work!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team at eXmoor Pharma!
How to prepare for a job interview at eXmoor Pharma Concepts Limited
✨Know Your GMP Basics
Make sure you brush up on your GMP knowledge before the interview. Understand the key principles of Good Manufacturing Practice and how they apply to cell and gene therapies. This will show that you're not just familiar with the terminology, but that you can also apply it in a practical setting.
✨Showcase Your Technical Skills
Be prepared to discuss your experience with mammalian cell culture, purification processes, and aseptic filling. Bring specific examples from your past work that demonstrate your hands-on skills and problem-solving abilities in these areas. This will help you stand out as a candidate who can hit the ground running.
✨Ask Insightful Questions
Prepare some thoughtful questions about eXmoor Pharma's projects and their approach to GMP production. This not only shows your interest in the role but also gives you a chance to assess if the company aligns with your career goals. Think about asking how they handle tech transfers or what challenges they face in scaling up production.
✨Emphasise Teamwork and Communication
Since this role involves working closely with various teams, highlight your teamwork and communication skills during the interview. Share examples of how you've successfully collaborated with others in a lab setting, and how you ensure clear documentation and adherence to SOPs. This will demonstrate that you're a team player who values collaboration.
