GMP Production Scientist in Bristol

Energy Jobline ZR; Bristol; On-site; GBP 30,000 - 45,000; Full time

Job summary

An innovative biopharmaceutical company in Bristol is seeking a GMP Production Scientist to support the operation of GMP production suites for ATMP clinical products. The role involves assisting in tech transfer, maintaining production standards, and ensuring compliance with GMP requirements. Ideal candidates have a BSc in Life Sciences and experience working within a GMP Quality system.

Qualifications

• Experience working within a GMP Quality system involving management of production deviations.
• Understanding or experience in mammalian cell culture and purification processes.
• Resilience and flexibility to contribute to solving processing problems.

Responsibilities

• Support routine operation of GMP production for ATMP clinical products.
• Assist in tech transfer and scale-up within GMP facility.
• Ensure compliance with GMP and documentation standards.

Skills

Organisation, planning and time management

Oral and written communication skills

Teamworking

Problem solving

Attention to detail

Proficiency in Office365

Education

BSc in Life Science or equivalent experience

Job description

Energy Jobline is the largest and fastest growing global Energy Job Board and Energy Hub. We have an audience reach of over 7 million energy professionals, 400,000+ monthly advertised global energy and engineering jobs, and work with the leading energy companies worldwide.

We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.

Job Description

Job title: GMP Production Scientist

Reporting to: Senior GMP Production Scientist

Department: GMP

No of Direct reports: 0

Summary:

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.

The GMP Production Scientists will carry out day-to-day production activities and routine clean room duties along with supporting the technology transfer of processes from eXmoor’s Process Development Teams.

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 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&GT, 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).

If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.