GMP Process Specialist

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,...

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...

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...

We are seeking an experienced GMP Compliance Manager to join our Manufacturing team on a 12-month fixed-term contract.About the roleThe purpose of this role is to work alongside the GMP Manufacturing teams to ensure timely completion of batch-related issues and compliance with internal and external GMP requirements.ResponsibilitiesLead investigations and...

Process Compliance Officer Job DescriptionWe are looking for a skilled Process Compliance Officer to join our Manufacturing team on a 12-month fixed-term contract. The primary responsibility 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...

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...

This is a unique opportunity for an experienced Compliance and Assurance Specialist to lead investigations and root cause analysis into process and facility deviations, conduct regular self-inspections of the Manufacturing department, and organise and facilitate individual and group training with regard to manufacturing SOPs and procedures.The estimated...

OXB, a pioneering viral vector CDMO, invites applications from experienced professionals for a GMP Compliance Coordinator role. This 12-month fixed-term contract offers the opportunity to work within a state-of-the-art laboratory and manufacturing environment.About the Role:The successful candidate will be responsible for coordinating compliance activities...

Join OXB, a leading viral vector CDMO, and contribute to the development of life-changing therapies for patients worldwide.OXB is at the forefront of the rapidly growing cell and gene therapy sector. As a "Validation Process Specialist", you will play a crucial role in ensuring the quality and safety of our manufacturing processes.About UsWe are a team of...

About the RoleThe successful candidate will lead investigations and root cause analysis into process and facility deviations, ensuring that all necessary steps are taken to resolve these issues in a timely manner.The ideal candidate will have experience working within a GMP pharmaceutical/biotechnology environment, with a strong understanding of regulatory...

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...

Job OverviewWe are seeking a Sterile Process Validation Lead to join our team at Oxford Biomedica. In this role, you will be responsible for validating sterile processes and ensuring compliance with GMP regulations.About the RoleThis is an exciting opportunity to contribute to the maintenance of overall department KPIs relating to validation of equipment,...

Job Title: MSAT Process Development LeadWe are working with a leading Life Science and clinical research company to find an experienced MSAT Process Development Lead.About the Company:Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. Our team has extensive experience in finding senior talent within the industry.About the...

Process Assurance Officer Job DescriptionWe are seeking a skilled Process Assurance Officer to join our Manufacturing team on a 12-month fixed-term contract. As a key member of our team, you will be responsible for ensuring timely completion of batch-related issues while maintaining compliance with internal and external GMP requirements.The estimated salary...

Compliance Process Lead Job DescriptionOxford Biomedica is seeking a highly skilled Compliance Process Lead to join our Manufacturing team on a 12-month fixed-term contract. As a key member of our team, you will be responsible for ensuring timely completion of batch-related issues while maintaining compliance with internal and external GMP requirements.The...

Job Title: Manufacturing Quality Assurance SpecialistWe are seeking a highly motivated Manufacturing Quality Assurance Specialist to join our team in Oxford, UK. The role is responsible for supporting the day-to-day activities within manufacturing and performing product release testing of medical devices.Key Responsibilities:Perform and document in-process...

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...

Job Title: Inspector of Manufacturing ProcessesSkill Alliance is seeking a highly skilled Inspector of Manufacturing Processes to join our team in Oxford, UK. The successful candidate will have a strong understanding of inspection criteria, use of drawings/specifications, and the ability to create and write SOPs and work instructions/specifications.Main...

Senior Analytical Development SpecialistIn this role, you will be responsible for the development and optimization of analytical methods to support biopharmaceutical drug development.Responsibilities:Manage the development and validation of analytical test methods and technology transfer in accordance with ICH guidelines.Support release and stability...

Job Description:We are seeking a highly skilled Quality Assurance Specialist to join our Analytical Development and QC Team.The purpose of this role is to ensure timely reporting of analytical data, support outsourced QC testing, and provide oversight of GMP compliance.Key Responsibilities:QC Issuing Assay PaperworkQC Checking of GMP DocumentationReporting...