Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- 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 over 20 years of expertise.
- Benefits: Gain hands-on experience, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in the biotech field while developing your career in GMP manufacturing.
- Qualifications: BSc in Life Science or equivalent experience; understanding of GMP processes.
- Other info: Collaborate with a globally recognised team and contribute to innovative projects.
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.
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
- Understanding GMP
- 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 employer: eXmoor pharma
Contact Detail:
eXmoor pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land GMP Production Scientist
✨Tip Number 1
Network like a pro! Reach out to professionals in the GMP and biopharmaceutical fields on LinkedIn. Join relevant groups, attend webinars, and don’t be shy 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 and understand their projects and values. Be ready to discuss how your skills in cell culture and GMP processes can contribute to their success. Practice common interview questions and have your own questions ready to show your interest.
✨Tip Number 3
Showcase your passion for the industry! During interviews, share your enthusiasm for cell and gene therapies. Talk about any relevant projects or experiences that highlight your problem-solving skills and attention to detail. Let them see your motivation to grow within the field.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got a streamlined application process that makes it easy for you to get your foot in the door. Plus, it shows you’re genuinely interested in joining our team at eXmoor Pharma!
We think you need these skills to ace GMP Production Scientist
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 do at eXmoor Pharma!
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. Keep it concise but engaging – we love a good story!
Showcase Your Attention to Detail: In the world of GMP, attention to detail is crucial. Make sure your application is free from typos and errors. This reflects your commitment to quality, which is something we value highly at eXmoor Pharma.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts!
