GMP Compliance Professional

Quality Assurance Specialist">This 12-month fixed-term contract role involves working closely with the GMP Manufacturing team to ensure batch-related issues are resolved promptly, while maintaining GMP compliance.About Our Organisation">Oxford Biomedica is a quality and innovation-led CDMO providing development and manufacturing expertise in lentivirus, AAV,...

About the OpportunityAre you an experienced GMP Compliance and Operations Manager looking for a new challenge? We are seeking a highly skilled individual to join our team at Oxford Biomedica.In this role, you will lead a team of GMP support assistants, coordinating daily activities to maintain process continuity and achieve production schedules while...

OXB, a quality and innovation-led viral vector CDMO, is a pioneer in cell and gene therapy with over 25 years of experience in viral vectors. We are recruiting for a GMP Compliance Officer Assistant to support our Manufacturing Support team.The successful candidate will work as part of a team to achieve the production support schedule with minimal disruption...

About the CompanyOxford Biomedica is a leading CDMO providing viral vector development and manufacturing expertise. Our mission is to enable clients to deliver life-changing therapies to patients around the world.Our ValuesResponsibleResponsiveResilientRespectWe offer a competitive total reward package, including a salary range of £60,000 - £80,000 per...

Job OverviewWe are seeking a highly skilled GMP Compliance Professional to join our Manufacturing team on a 12-month fixed-term contract. The primary objective of this role is to collaborate with our GMP Manufacturing teams to ensure timely resolution of batch-related issues and adherence to internal and external GMP requirements.Main Responsibilities:Lead...

Role Overview">The Process Compliance Officer will work alongside the GMP Manufacturing teams to ensure timely completion of batch related issues, while maintaining compliance with internal and external GMP requirements.About This Role">This role involves leading investigations and root cause analysis into process and facility deviations, conducting regular...

About the RoleWe are currently recruiting for a skilled Regulatory Compliance Specialist to join our Manufacturing team on a 12-month fixed-term contract. The primary goal of this role is to collaborate with our GMP Manufacturing teams to ensure timely resolution of batch-related issues and adherence to internal and external GMP requirements.Main...

We are a pioneer in the rapidly growing cell and gene therapy sector, delivering life-changing therapies to patients worldwide.Our Analytical Development and QC (ADQC) Team is seeking a highly skilled Cell and Gene Therapy Compliance Specialist to ensure timely reporting of analytical data, support outsourced QC testing, and provide oversight of GMP...

Job DescriptionWe have an exciting opportunity for a Quality Assurance Technician to join our global client's team in the pharmaceutical industry.The successful candidate will be responsible for contributing to ongoing projects and performing equipment tests, following SOPs and ensuring health and safety compliance.Responsibilities and...

Job Overview:OXB is a quality and innovation-led viral vector CDMO with a mission to enable clients to deliver life-changing therapies to patients around the world.This is an exciting opportunity to join our team as an Analytical Compliance Manager and contribute to the development of new viral vectors.Responsibilities:Supporting QC TestingProviding...

About the RoleThe Senior Scientist - Analytical Development will play a critical role in supporting the development of new analytical test methods and technology transfer, ensuring compliance with ICH and other regulatory guidances. This position will also involve managing release and stability testing, directing good manufacturing practices (GMP)...

GMP Compliance Specialist">This 12-month fixed-term contract role involves working closely with the GMP Manufacturing team to ensure batch-related issues are resolved promptly, while maintaining GMP compliance.About Our Team">Oxford Biomedica is a pioneering CDMO delivering high-quality viral vector development and manufacturing services.We partner with...

We are seeking an experienced QC Compliance Officer II to join our team and contribute to our mission of delivering life-changing therapies to patients worldwide.In this role, you will be responsible for ensuring timely reporting of analytical data, supporting outsourced QC testing, and providing oversight of GMP compliance.About the Job:Work closely with...

OXB, a quality and innovation-led viral vector CDMO, is seeking a Director of Quality Systems Compliance to lead the company's quality processes and systems compliance with GMP guidelines.The successful candidate will be responsible for maintaining GXP regulations compliance support and guidance to OXB GXP functions. This includes leading internal and...

About the RoleWe are seeking an experienced Biotech Manufacturing Team Lead to join our team at Oxford Biomedica. The ideal candidate will have a strong background in GMP compliance and operations management.As a key member of our manufacturing team, you will be responsible for leading a team of GMP support assistants, coordinating daily cleaning, waste...

We are seeking an experienced Viral Vector Production Support Associate to join our Manufacturing Support team at OXB, a leading viral vector CDMO. The role involves working as part of a team in day-to-day production support activities, ensuring process continuity while maintaining GMP, safety, and environmental compliance.Key responsibilities...

Job OverviewWe are seeking a Quality Assurance Technician to join our global CDMO clients' team.The successful candidate will contribute to ongoing projects and perform equipment tests, following Standard Operating Procedures (SOPs) while ensuring health and safety compliance.About the Role:The ideal candidate should have a quality background and knowledge...

Job Title: Compliance AdministrationWe are seeking an experienced Recruitment Consultant to work in Didcot. This is a fantastic opportunity for someone with previous recruitment experience and strong business development, account management, and target-driven skills.The ideal candidate will have a proven track record of registering and interviewing...

We are seeking a highly skilled Viral Vector Manufacturing Specialist to join our team at Oxford Biomedica. In this role, you will work as part of a team in the day-to-day production support activities, ensuring process continuity while maintaining GMP, safety, and environmental compliance.About UsOxford Biomedica is a leading provider of viral vector-based...

About the Role:We are seeking a highly skilled QC Compliance Officer II to join our Analytical Development and QC (ADQC) Team. The purpose of this role is to ensure timely reporting of analytical data, support outsourced QC testing, and provide oversight of GMP compliance.The successful candidate will have a degree in Life Sciences and experience working...