GMP Validation 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,...

Job DescriptionWe are seeking a highly skilled Biopharmaceutical Validation Expert to join our team at Oxford Biomedica. In this role, you will be responsible for preparing and executing validation protocols and reports for Process Validation/Process Performance Qualification (PPQ). You will also own quality records on behalf of the Validation Department and...

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,...

About the RoleWe are seeking a skilled Chromatography Data System (CDS) Specialist to join our team at Hyper Recruitment Solutions in the Oxford area.As a CDS Specialist, you will be responsible for ensuring the successful introduction and validation of the Chromatography Data System with a focus on Computer System Validation (CSV).

We are seeking a Data Validation Specialist to join our team at Hyper Recruitment Solutions. This exciting role will focus on the introduction and validation of Chromatography Data Systems with a strong emphasis on Computer System Validation (CSV).**Key Responsibilities:**The ideal candidate will be responsible for overseeing the implementation and...

About the Role: IC Resources is seeking an accomplished Principal Validation Specialist to drive the development of cutting-edge ASICs for prominent clients in the UK.Key Responsibilities:To spearhead the validation process for advanced ASIC designs using innovative methodologies.To create and execute validation strategies that meet customer demands.To...

We are looking for a highly motivated and detail-oriented Automotive Validation Specialist to join our Total Vehicle Validation and Integration team at Rolls-Royce Motor Cars, Goodwood.About the RoleThis is an exciting opportunity to work as part of a strong unit where every opinion is valued. You will have the chance to gain hands-on experience in various...

We are looking for a highly skilled Validation Specialist to join our team at Hyper Recruitment Solutions. As a key member of our team, you will be responsible for validating qPCR systems to ensure they meet regulatory requirements and industry standards.Key Tasks:Develop and execute validation protocols for qPCR systems.Collaborate with cross-functional...

About the RoleWe are seeking a highly skilled Test and Validation Specialist to join our Mechanical Systems and Test department. As a key member of the team, you will report to the Principal Engineer for Mechanical Test and Validation and support multiple projects across the heavy industry and mobility sectors.Main ResponsibilitiesAssist Senior or Principal...

Job Title: Senior Asset ScientistWe are looking for a highly experienced AML Target Validation Specialist to join our team at Immunocore. As a Senior Asset Scientist, you will be responsible for validating AML targets and contributing to the development of innovative precision engineered drugs.About the JobYou will work independently as a representative of...

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...

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...

About OrganOxOrganOx is a pioneering medical device company that has been revolutionizing organ transplantation since 2008. Our innovative technology, such as the OrganOx metra, leverages normothermic machine perfusion to preserve donor livers for up to 24 hours, significantly reducing organ discard rates and improving transplant success.Salary Range:...

**Job Description:**As a Senior Quality Control Specialist at Oxford Biomedica, you will play a vital role in ensuring the quality of our GMP testing operations and manufacturing processes. This includes reviewing quality systems documentation, providing QA support, and conducting walk rounds/inspections in QC laboratories or GMP manufacturing...

Job OverviewWe are looking for a highly skilled Senior Scientist to join our team in Oxfordshire, where you will be responsible for leading the development of analytical methods for biopharmaceutical products.Key Responsibilities:Manage the development, qualification, and validation of analytical test methods and technology transfer.Support the...

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...

Company OverviewWe are a leading pharmaceutical company in Oxford seeking a Quality Control Specialist to join our team. As a quality control specialist, you will be responsible for preparing and conducting quality control assessments on radiopharmaceuticals, while providing support for the maintenance and operation of the Radiopharmacy, adhering to GMP...

About the RoleWe are seeking a highly motivated Quality Assurance Specialist II to join our Analytical Development and QC (ADQC) Team.Job OverviewThe successful candidate will be responsible for ensuring timely reporting of analytical data, supporting outsourced QC testing, and providing oversight of GMP compliance.Key ResponsibilitiesCreate sample...

About the RoleWe are looking for a highly skilled Biotech Research Associate to join our Target Identification and Validation team. As a key member of our team, you will play a crucial role in developing and implementing innovative solutions to drive research forward.Job SummaryThis is an exciting opportunity for a collaborative and enthusiastic junior...

About the RoleWe are seeking a dedicated and detail-oriented Bioinformatics Quality Assurance Specialist to join our team at Oxford Nanopore Technologies. This is an exciting opportunity to work on cutting-edge bioinformatics software and to contribute to the development of high-quality products.In this role, you will be responsible for implementing QA...