OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. An opportunity has arisen in our Medical Affairs team for a Medical Affairs QC Analyst. This role offers a varied mix of hands on laboratory work and quality-focused administrative responsibilities, supporting key FISH and NGS processing activities. What you'll be doing for us: Responsible for an assigned proportion of FISH and NGS product testing Act as a subject expert in microscopy and NGS process for the purposes of product testing Adhering to documented procedures for all aspects of laboratory work, ensuring that all relevant information is recorded, products and samples are handled correctly, and that all necessary records and quality data are maintained. Responsible for an appropriate proportion of the quality management system, including procedures and audits. Oversee the smooth and efficient functioning of the laboratory, together with the other MA team members, including consumables, reagents, microscopes, equipment, and software. Contribute to the documentation and infrastructure of the department by providing input into internal protocols and implementation of CAPAs and improvements. Assist with investigations of product, process and equipment nonconformities, validations and process -efficiency initiatives. To comply with all site quality management systems, regulations and health and safety procedures (ISO 9001:2015, ISO 13485:2016, ISO 27001:2022, (EU) 2017/746 (IVDR), GCLP and Human Tissue Act (2004 To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager. What we are looking for in you: A bachelor's degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required, with a minimum of one-year laboratory experience Experience of working in a GLP/GMP environment Basic knowledge of FISH Basic Knowledge of NGS High accuracy and attention to detail Familiarity with working to defined protocols or standard operating procedures (SOPs) Able to work accurately and efficiently in a high-volume, process-driven, and protocol-driven environment Strong team work ethic and commitment to successfully deliver to tight deadlines are essential. Previous experience with FISH analysis is highly advantageous Experience in microscopy is advantageous Proficiency in molecular biology techniques is highly advantageous Experience in NGS based analysis is advantageous. In return you will receive: Private Health Insurance Group Income Protection Group Life Assurance High Street Discount Scheme. Application is via CV and a one-page covering letter outlining your suitability for the role, salary expectations and notice period. Please note that we will need to establish your right to work during the recruitment process.
May 30, 2026
Full time
OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. An opportunity has arisen in our Medical Affairs team for a Medical Affairs QC Analyst. This role offers a varied mix of hands on laboratory work and quality-focused administrative responsibilities, supporting key FISH and NGS processing activities. What you'll be doing for us: Responsible for an assigned proportion of FISH and NGS product testing Act as a subject expert in microscopy and NGS process for the purposes of product testing Adhering to documented procedures for all aspects of laboratory work, ensuring that all relevant information is recorded, products and samples are handled correctly, and that all necessary records and quality data are maintained. Responsible for an appropriate proportion of the quality management system, including procedures and audits. Oversee the smooth and efficient functioning of the laboratory, together with the other MA team members, including consumables, reagents, microscopes, equipment, and software. Contribute to the documentation and infrastructure of the department by providing input into internal protocols and implementation of CAPAs and improvements. Assist with investigations of product, process and equipment nonconformities, validations and process -efficiency initiatives. To comply with all site quality management systems, regulations and health and safety procedures (ISO 9001:2015, ISO 13485:2016, ISO 27001:2022, (EU) 2017/746 (IVDR), GCLP and Human Tissue Act (2004 To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager. What we are looking for in you: A bachelor's degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required, with a minimum of one-year laboratory experience Experience of working in a GLP/GMP environment Basic knowledge of FISH Basic Knowledge of NGS High accuracy and attention to detail Familiarity with working to defined protocols or standard operating procedures (SOPs) Able to work accurately and efficiently in a high-volume, process-driven, and protocol-driven environment Strong team work ethic and commitment to successfully deliver to tight deadlines are essential. Previous experience with FISH analysis is highly advantageous Experience in microscopy is advantageous Proficiency in molecular biology techniques is highly advantageous Experience in NGS based analysis is advantageous. In return you will receive: Private Health Insurance Group Income Protection Group Life Assurance High Street Discount Scheme. Application is via CV and a one-page covering letter outlining your suitability for the role, salary expectations and notice period. Please note that we will need to establish your right to work during the recruitment process.
OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. This position is a fixed-term contract ending in December 2028 What you'll be doing for us: Ensure smooth and efficient running of the laboratory, including consumables, reagents, microscopes, equipment and software within the MA team Process FISH workload, using FFPE, haematological and prenatal specimens to support QC and studies in the medical affairs team Responsible for sample receipt, release, shipment, storage and disposal following standard operating procedures (SOPs) and adhering to the Human Tissue Act (2004) Laboratory duties such as biological sample culturing, harvesting, and fixed cell slide preparation Sectioning of FFPE tissue blocks and FFPE slide preparation Maintain laboratory records and LIMS, making sure they are up to date and accurate Perform image capture of FISH slides using automation or manual methods Support with maintaining appropriate proportion of the quality management system, including procedures and audits To comply with all site quality management systems, regulations and health and safety procedures (ISO 9001:2015, ISO 13485:2016, ISO 27001:2022, (EU) 2017/746 (IVDR), GCLP and Human Tissue Act (2004 To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager. What we are looking for in you Abachelor's degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject OR a minimum of one year laboratory experience Basic knowledge of FISH processing High accuracy and attention to detail Ability to work independently on routine tasks, while knowing when to seek support Able to work accurately and efficiently in a high-volume, process-driven, and protocol-driven environment Strong Communication skills, both written and verbal. Previous experience with FISH Experience with microscopy and microtomy Experience in cell culture techniques Knowledge and previous use of a LIMS Familiarity with working to defined protocols or standard operating procedures (SOPs). In return you will receive: Private Health Insurance Group Income Protection Group Life Assurance High Street Discount Scheme.
May 30, 2026
Full time
OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. This position is a fixed-term contract ending in December 2028 What you'll be doing for us: Ensure smooth and efficient running of the laboratory, including consumables, reagents, microscopes, equipment and software within the MA team Process FISH workload, using FFPE, haematological and prenatal specimens to support QC and studies in the medical affairs team Responsible for sample receipt, release, shipment, storage and disposal following standard operating procedures (SOPs) and adhering to the Human Tissue Act (2004) Laboratory duties such as biological sample culturing, harvesting, and fixed cell slide preparation Sectioning of FFPE tissue blocks and FFPE slide preparation Maintain laboratory records and LIMS, making sure they are up to date and accurate Perform image capture of FISH slides using automation or manual methods Support with maintaining appropriate proportion of the quality management system, including procedures and audits To comply with all site quality management systems, regulations and health and safety procedures (ISO 9001:2015, ISO 13485:2016, ISO 27001:2022, (EU) 2017/746 (IVDR), GCLP and Human Tissue Act (2004 To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager. What we are looking for in you Abachelor's degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject OR a minimum of one year laboratory experience Basic knowledge of FISH processing High accuracy and attention to detail Ability to work independently on routine tasks, while knowing when to seek support Able to work accurately and efficiently in a high-volume, process-driven, and protocol-driven environment Strong Communication skills, both written and verbal. Previous experience with FISH Experience with microscopy and microtomy Experience in cell culture techniques Knowledge and previous use of a LIMS Familiarity with working to defined protocols or standard operating procedures (SOPs). In return you will receive: Private Health Insurance Group Income Protection Group Life Assurance High Street Discount Scheme.
About OGT OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. This position is a fixed term contract, ending in December 2028 Responsibilities Contribute to the documentation and infrastructure of the department by overseeing the writing of internal and external protocols, study plans and reports Participate in the design, implementation and delivery of any required studies Identify and engage external laboratories, clinicians, and partners to obtain clinical performance data Support and coordinate external studies, including collaboration, data sharing, and contracting activities Collaborate with internal and external stakeholders to support project delivery Manage and coordinate projects activities from initiation through to completion Analyse and interpret data across diagnostic techniques and deliver scientific, clinical, and analytical reports in a timely manner Ensure timely and accurate reporting of study results Provide clinical/scientific input for product brochures, catalogues and other marketing materials when required Contribute to the quality management system and infrastructure of the department by providing input into internal protocols and implementation of CAPAs, change controls and improvements Support validation activities for team equipment and software, and support maintenance of risk management documentation in line with ISO 14971 Provide training and support to medical affairs analysts and assistants as appropriate Provision of analytical teaching within and outside of the medical affairs team as appropriate Analysis of FFPE and haematological specimens using manual microscopes and automated software Support karyotype analysis of G banding and reverse DAPI FISH images To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager Qualifications A bachelor's degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required Knowledge of FISH and/or cytogenetics techniques and their clinical applications Understanding of clinical diagnostics, laboratory workflows, or molecular testing Ability to engage confidently with external partners, including laboratories, clinicians, and collaborators Proven ability to proactively drive activities forward Experience drafting study protocols or similar technical/scientific documentation Understanding of study design considerations, including objectives, endpoints and data requirements Strong organisational and project coordination skills, managing activities from initiation through to completion Ability to interpret clinical or diagnostic data, including comparison across different testing methodologies Experience handling sensitive or clinical data, with an understanding of data quality and governance requirements Excellent communication skills, both written and verbal Cytogenetics experience in an NHS laboratory or equivalent Experience in data acquisition, clinical studies, or external collaborations Experience setting up or supporting contracts, agreements, or study arrangements with external partners Familiarity with disease areas, sample types, and appropriate testing approaches Awareness of commercial or customer facing environments, particularly in diagnostics or life sciences Experience supporting clinical performance evaluations, validation, or regulatory activities Experience in cytogenetics and or Karyotype analysis Benefits Private Health Insurance Group Income Protection Group Life Assurance High Street Discount Scheme Additional Information In order to proceed with the recruitment process, we will need to establish your right to work in the UK. Please note that we are unable to sponsor any visa applications at this time and applicants must have the right to work in the UK.
May 30, 2026
Full time
About OGT OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. This position is a fixed term contract, ending in December 2028 Responsibilities Contribute to the documentation and infrastructure of the department by overseeing the writing of internal and external protocols, study plans and reports Participate in the design, implementation and delivery of any required studies Identify and engage external laboratories, clinicians, and partners to obtain clinical performance data Support and coordinate external studies, including collaboration, data sharing, and contracting activities Collaborate with internal and external stakeholders to support project delivery Manage and coordinate projects activities from initiation through to completion Analyse and interpret data across diagnostic techniques and deliver scientific, clinical, and analytical reports in a timely manner Ensure timely and accurate reporting of study results Provide clinical/scientific input for product brochures, catalogues and other marketing materials when required Contribute to the quality management system and infrastructure of the department by providing input into internal protocols and implementation of CAPAs, change controls and improvements Support validation activities for team equipment and software, and support maintenance of risk management documentation in line with ISO 14971 Provide training and support to medical affairs analysts and assistants as appropriate Provision of analytical teaching within and outside of the medical affairs team as appropriate Analysis of FFPE and haematological specimens using manual microscopes and automated software Support karyotype analysis of G banding and reverse DAPI FISH images To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager Qualifications A bachelor's degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required Knowledge of FISH and/or cytogenetics techniques and their clinical applications Understanding of clinical diagnostics, laboratory workflows, or molecular testing Ability to engage confidently with external partners, including laboratories, clinicians, and collaborators Proven ability to proactively drive activities forward Experience drafting study protocols or similar technical/scientific documentation Understanding of study design considerations, including objectives, endpoints and data requirements Strong organisational and project coordination skills, managing activities from initiation through to completion Ability to interpret clinical or diagnostic data, including comparison across different testing methodologies Experience handling sensitive or clinical data, with an understanding of data quality and governance requirements Excellent communication skills, both written and verbal Cytogenetics experience in an NHS laboratory or equivalent Experience in data acquisition, clinical studies, or external collaborations Experience setting up or supporting contracts, agreements, or study arrangements with external partners Familiarity with disease areas, sample types, and appropriate testing approaches Awareness of commercial or customer facing environments, particularly in diagnostics or life sciences Experience supporting clinical performance evaluations, validation, or regulatory activities Experience in cytogenetics and or Karyotype analysis Benefits Private Health Insurance Group Income Protection Group Life Assurance High Street Discount Scheme Additional Information In order to proceed with the recruitment process, we will need to establish your right to work in the UK. Please note that we are unable to sponsor any visa applications at this time and applicants must have the right to work in the UK.
