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TRS Consulting
Technical Support Engineer, Medical Pathology Analysers
TRS Consulting Wavendon, Bedfordshire
Technical Support Engineer, Medical Pathology Analysers Overall Earnings £43,500 Basic Salary £37,500 Bonus £6,000 Excellent Benefits Package A hybrid working role with the option of two days a week from home and three in the office Hours are 37.5 per week, Monday Friday The Role Technical Support Engineer, Medical Pathology Analysers This market leader seeks to recruit a technically motivated and customer focused Technical Support Engineer, responsible for: Providing technical support and first line technical fixes via telephone and by using connectivity tools Supporting customers with technical issues on a range of medical diagnostic analysers Guiding users through troubleshooting via phone and video calls Escalating unresolved technical issues to the Field Service Engineering team Your Background Technical Support Engineer, Medical Pathology Analysers To succeed in this exciting role, you must be able to demonstrate: A competent background in a service engineering capacity gained within any high value capital equipment environment Applications are encouraged from engineers with a broad range of backgrounds, including laboratory device, medical device, pharmaceutical device, ex forces engineers (medical & dental, weapons systems, radar) and a wide range of other electronic or electro-mechanical from other sectors A qualification in engineering, electronics or a science based subject to a minimum of ONC level Applicants are welcome from field service engineers from a broad base of sectors, as full and comprehensive product training will be provided The Company Technical Support Engineer, Medical Pathology Analysers Well respected supplier of sophisticated medical diagnostics systems, trusted by healthcare professionals to accurately diagnose and test patients for a wide range of medical conditions and diseases This instantly recognisable brand leader supplies a wide range of innovative diagnostic based laboratory and medical systems to the healthcare sector, and offers 'best in class' solutions across their range of products and systems, which include applications for microbiology, immunodiagnostics, molecular diagnostics and blood bank screening Supported by a truly multi-national 'blue-chip' technology group with representation in over 150 countries, their commitment to investment in Research and Development is second to none in their industry, ensuring that they remain a market leader At the core of their business lie product innovation, excellent customer service and good people This vacancy is being advertised by TRS Consulting. The services advertised by TRS Consulting are those of an employment agency and / or employment business.
28/07/2026
Full time
Technical Support Engineer, Medical Pathology Analysers Overall Earnings £43,500 Basic Salary £37,500 Bonus £6,000 Excellent Benefits Package A hybrid working role with the option of two days a week from home and three in the office Hours are 37.5 per week, Monday Friday The Role Technical Support Engineer, Medical Pathology Analysers This market leader seeks to recruit a technically motivated and customer focused Technical Support Engineer, responsible for: Providing technical support and first line technical fixes via telephone and by using connectivity tools Supporting customers with technical issues on a range of medical diagnostic analysers Guiding users through troubleshooting via phone and video calls Escalating unresolved technical issues to the Field Service Engineering team Your Background Technical Support Engineer, Medical Pathology Analysers To succeed in this exciting role, you must be able to demonstrate: A competent background in a service engineering capacity gained within any high value capital equipment environment Applications are encouraged from engineers with a broad range of backgrounds, including laboratory device, medical device, pharmaceutical device, ex forces engineers (medical & dental, weapons systems, radar) and a wide range of other electronic or electro-mechanical from other sectors A qualification in engineering, electronics or a science based subject to a minimum of ONC level Applicants are welcome from field service engineers from a broad base of sectors, as full and comprehensive product training will be provided The Company Technical Support Engineer, Medical Pathology Analysers Well respected supplier of sophisticated medical diagnostics systems, trusted by healthcare professionals to accurately diagnose and test patients for a wide range of medical conditions and diseases This instantly recognisable brand leader supplies a wide range of innovative diagnostic based laboratory and medical systems to the healthcare sector, and offers 'best in class' solutions across their range of products and systems, which include applications for microbiology, immunodiagnostics, molecular diagnostics and blood bank screening Supported by a truly multi-national 'blue-chip' technology group with representation in over 150 countries, their commitment to investment in Research and Development is second to none in their industry, ensuring that they remain a market leader At the core of their business lie product innovation, excellent customer service and good people This vacancy is being advertised by TRS Consulting. The services advertised by TRS Consulting are those of an employment agency and / or employment business.
Development - Development Technologist
Finsbury Food Hamilton, Lanarkshire
We have an exciting opportunity to join the Development team in the role ofDevelopment Technologist at our Lightbody site as part of Finsbury Food Group. With over 135 years of craft baking heritage, Lightbody is proud to be the UK's largest supplier of celebration cakes. From branded favourites like Disney, Mars, Universal and Thorntons to supermarket own-label products, we produce over 55 million cakes and sweet treats every year right here in Hamilton. As a Development Technologist, you willbe responsible to develop, trial and validate new and existing products in line with agreed customer briefs, commercial targets and factory capability. The role plays a key part in accurate costings, robust documentation, effective risk management and smooth translation from concept through to factory launch, while supporting innovation, food safety, quality and continuous improvement standards. This is what you'll actually do! As a Development Technologist, you will drive innovative product development from concept to launch, ensuring compliance with legal, brand and customer standards. You will work with your cake designers to capture and manage cost-effective recipes through our recipe management system, ensuring they are aligned to margin and nutritional targets. You will produce accurate trial documentation and factory handover packs, and be responsible for QAS and arranging customer samples. You will plan and coordinate factory trials, capturing key data, managing risks and delivering clear, evidence-based recommendations. Working closely with Technical and cross-functional teams, you will support product validation including shelf-life, microbiological and physical testing. You will benchmark products against the market, identify opportunities for improvement and contribute to continuous innovation and process excellence. Flexibility in working hours is required to support factory trials and launch activities. Ideally this is you! Degree preferred Food Science / Technology / Process Engineering or similar degree / HND equivalent or relevant experience Strong understanding of product development processes from concept to launch Knowledge of factory processes and manufacturability considerations Experience generating recipes, costings and managing BoMs Ability to manage multiple projects to critical path deadlines Strong analytical skills with ability to interpret trial and validation data Knowledge of food safety, microbiology and shelf-life validation Commercial awareness and understanding of margin targets Strong communication and stakeholder management skills Passion for food innovation and emerging market trends Detail-oriented, organised and solutions-focused Valid UK driving license preferred What'sin it for you! Enhanced Maternity & Paternity Leave to allow quality time with your new arrival! Enhanced Pension Scheme for our employees Free Employee AssistanceProgramme(open to colleagues and their families) Retail discounts accessible via our Benefits Hub platform! Refer a Friend Scheme (up to £300 per referral - T&C's dependent) Employee Recognition Awards Extensive Learning & Development opportunities (including opportunities for sponsored professional memberships and our own in-house development course!) An opportunity to be part of a fantastic, growingorganisation. Our vision is to be the leading specialty bakery group in the UK, and we want the best people in place to achieve this. Our continued success is built entirely on the talented people who work here, so employee development is important to us because everyone is a valued member of the team, and we want every individual to have the skills and capabilities to achieve both your own personal goals and our business goals. We want good people to join our company, to help our company continue to go from strength to strength.
26/07/2026
Full time
We have an exciting opportunity to join the Development team in the role ofDevelopment Technologist at our Lightbody site as part of Finsbury Food Group. With over 135 years of craft baking heritage, Lightbody is proud to be the UK's largest supplier of celebration cakes. From branded favourites like Disney, Mars, Universal and Thorntons to supermarket own-label products, we produce over 55 million cakes and sweet treats every year right here in Hamilton. As a Development Technologist, you willbe responsible to develop, trial and validate new and existing products in line with agreed customer briefs, commercial targets and factory capability. The role plays a key part in accurate costings, robust documentation, effective risk management and smooth translation from concept through to factory launch, while supporting innovation, food safety, quality and continuous improvement standards. This is what you'll actually do! As a Development Technologist, you will drive innovative product development from concept to launch, ensuring compliance with legal, brand and customer standards. You will work with your cake designers to capture and manage cost-effective recipes through our recipe management system, ensuring they are aligned to margin and nutritional targets. You will produce accurate trial documentation and factory handover packs, and be responsible for QAS and arranging customer samples. You will plan and coordinate factory trials, capturing key data, managing risks and delivering clear, evidence-based recommendations. Working closely with Technical and cross-functional teams, you will support product validation including shelf-life, microbiological and physical testing. You will benchmark products against the market, identify opportunities for improvement and contribute to continuous innovation and process excellence. Flexibility in working hours is required to support factory trials and launch activities. Ideally this is you! Degree preferred Food Science / Technology / Process Engineering or similar degree / HND equivalent or relevant experience Strong understanding of product development processes from concept to launch Knowledge of factory processes and manufacturability considerations Experience generating recipes, costings and managing BoMs Ability to manage multiple projects to critical path deadlines Strong analytical skills with ability to interpret trial and validation data Knowledge of food safety, microbiology and shelf-life validation Commercial awareness and understanding of margin targets Strong communication and stakeholder management skills Passion for food innovation and emerging market trends Detail-oriented, organised and solutions-focused Valid UK driving license preferred What'sin it for you! Enhanced Maternity & Paternity Leave to allow quality time with your new arrival! Enhanced Pension Scheme for our employees Free Employee AssistanceProgramme(open to colleagues and their families) Retail discounts accessible via our Benefits Hub platform! Refer a Friend Scheme (up to £300 per referral - T&C's dependent) Employee Recognition Awards Extensive Learning & Development opportunities (including opportunities for sponsored professional memberships and our own in-house development course!) An opportunity to be part of a fantastic, growingorganisation. Our vision is to be the leading specialty bakery group in the UK, and we want the best people in place to achieve this. Our continued success is built entirely on the talented people who work here, so employee development is important to us because everyone is a valued member of the team, and we want every individual to have the skills and capabilities to achieve both your own personal goals and our business goals. We want good people to join our company, to help our company continue to go from strength to strength.
TRS Consulting (UK) Ltd
Technical Support Engineer, Medical Pathology Analysers
TRS Consulting (UK) Ltd Milton Keynes, Buckinghamshire
Technical Support Engineer, Medical Pathology Analysers This market leader seeks to recruit a technically motivated and customer focused Technical Support Engineer, responsible for: Compensation Overall Earnings £43,500 Basic Salary £37,500 Bonus £6,000 Excellent Benefits Package Working Arrangement A hybrid working role with the option of two days a week from home and three in the office. Hours Hours are 37.5 per week, Monday - Friday. Responsibilities Providing technical support and first line technical fixes via telephone and using connectivity tools. Supporting customers with technical issues on a range of medical diagnostic analysers. Guiding users through troubleshooting via phone and video calls. Escalating unresolved technical issues to the Field Service Engineering team. Qualifications A competent background in a service engineering capacity gained within any high value capital equipment environment. Applications are encouraged from engineers with a broad range of backgrounds, including laboratory device, medical device, pharmaceutical device, ex forces engineers (medical & dental, weapons systems, radar) and a wide range of other electronic or electro-mechanical from other sectors. A qualification in engineering, electronics or a science based subject to a minimum of ONC level. Applicants are welcome from field service engineers from a broad base of sectors, as full and comprehensive product training will be provided. Company Well respected supplier of sophisticated medical diagnostics systems, trusted by healthcare professionals to accurately diagnose and test patients for a wide range of medical conditions and diseases. This instantly recognisable brand leader supplies a wide range of innovative diagnostic based laboratory and medical systems to the healthcare sector, and offers 'best in class' solutions across their range of products and systems, which include applications for microbiology, immunodiagnostics, molecular diagnostics and blood bank screening. Supported by a truly multi-national 'blue-chip' technology group with representation in over 150 countries, their commitment to investment in Research and Development is second to none in their industry, ensuring that they remain a market leader. At the core of their business lie product innovation, excellent customer service and good people.
26/07/2026
Full time
Technical Support Engineer, Medical Pathology Analysers This market leader seeks to recruit a technically motivated and customer focused Technical Support Engineer, responsible for: Compensation Overall Earnings £43,500 Basic Salary £37,500 Bonus £6,000 Excellent Benefits Package Working Arrangement A hybrid working role with the option of two days a week from home and three in the office. Hours Hours are 37.5 per week, Monday - Friday. Responsibilities Providing technical support and first line technical fixes via telephone and using connectivity tools. Supporting customers with technical issues on a range of medical diagnostic analysers. Guiding users through troubleshooting via phone and video calls. Escalating unresolved technical issues to the Field Service Engineering team. Qualifications A competent background in a service engineering capacity gained within any high value capital equipment environment. Applications are encouraged from engineers with a broad range of backgrounds, including laboratory device, medical device, pharmaceutical device, ex forces engineers (medical & dental, weapons systems, radar) and a wide range of other electronic or electro-mechanical from other sectors. A qualification in engineering, electronics or a science based subject to a minimum of ONC level. Applicants are welcome from field service engineers from a broad base of sectors, as full and comprehensive product training will be provided. Company Well respected supplier of sophisticated medical diagnostics systems, trusted by healthcare professionals to accurately diagnose and test patients for a wide range of medical conditions and diseases. This instantly recognisable brand leader supplies a wide range of innovative diagnostic based laboratory and medical systems to the healthcare sector, and offers 'best in class' solutions across their range of products and systems, which include applications for microbiology, immunodiagnostics, molecular diagnostics and blood bank screening. Supported by a truly multi-national 'blue-chip' technology group with representation in over 150 countries, their commitment to investment in Research and Development is second to none in their industry, ensuring that they remain a market leader. At the core of their business lie product innovation, excellent customer service and good people.
Genomic Applications Manager
Oxford Nanopore Technologies Ltd. Oxford, Oxfordshire
Work Type & Model: Hybrid - FTC (Maternity Cover) We are looking for a highly motivated individual to join our UK Applications team for maternity cover as a Genomic Applications Manager. This role will be based in Oxford and the successful candidate will lead and manage a proof-of-concept team. About Oxford Nanopore Technologies Oxford Nanopore Technologies is headquartered at the Oxford Science Park outside Oxford, UK, with satellite offices and a commercial presence in many global locations across the US, APAC, and Europe. Our goal is to enable the analysis of any living thing, by anyone, anywhere. We employ individuals from multiple subject areas, including nanopore science, molecular biology and applications, informatics, engineering, electronics, manufacturing, and commercialisation. Our sequencing platform is the only technology that offers real-time analysis, in fully scalable formats from pocket to population scale. This platform can analyze native DNA or RNA and sequence any length of fragment to achieve short to ultra-long read lengths. We aim to inspire anyone to sequence anything, anywhere. Do you want to be part of that? Role Summary Reporting to the Snr. Director, Genomic Applications, the successful candidate will lead and manage a team responsible for delivering proof-of-concept studies across a range of applied market segments. The team will evaluate the performance of nanopore sequencing in new applications, identify technical or workflow gaps, and provide initial solutions or assessments of how these gaps can be addressed. This role will involve designing and overseeing experimental studies, analysing results, and generating high-quality data packages and presentations to support internal decision making and customer engagement. The successful candidate will work closely with cross-functional teams in Oxford to remain aligned with the latest technology developments and to help assess the suitability of emerging nanopore capabilities for new applications and markets. Other responsibilities include Leading and managing a laboratory-based proof-of-concept team within Genomic Applications Designing and executing proof-of-concept studies to evaluate nanopore sequencing performance in new applied market applications Identifying workflow, assay, or technology gaps and proposing potential solutions or development pathways Supporting the assessment and early-stage development of new sequencing applications using ONT's nanopore platform Preparation and QC of sequencing analytes and libraries for experimental studies Analysing and interpreting experimental data, including basic bioinformatic analysis where appropriate Generating clear summaries, reports, and presentation materials to communicate findings to internal stakeholders Collaborating with internal scientific and product development teams to support application evaluation and technology adoption Managing laboratory activities, supporting team development, and assisting junior scientists with experimental and analytical tasks Contributing to the continuous improvement of laboratory workflows, experimental design, and proof-of-concept evaluation processes What We're Looking For We'll expect you to have undertaken successful experimental research from initial concept through to execution and interpretation. This should include experience with DNA and/or RNA manipulation and preferably next-generation sequencing technologies. You will have strong knowledge of molecular biology techniques and sequencing workflows, including sample preparation, library preparation, and quality control methods. Experience in evaluating new technologies, troubleshooting experimental workflows, and identifying practical solutions to technical challenges would be highly advantageous. You should be comfortable working across multiple projects simultaneously and capable of leading and motivating a scientific team in a fast-paced environment. In addition, you will possess excellent communication and problem-solving skills and be able to clearly present scientific findings to a range of audiences. A PhD in molecular biology, genetics, genomics, microbiology, or a related discipline is required, ideally alongside relevant postdoctoral and/or biotechnology industry experience. This role will suit a proactive, organised, and scientifically curious individual with a collaborative approach and the ability to lead effectively in a dynamic environment. Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the duties of the job. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. About Us Oxford Nanopore Technologies: Our goal is to bring the widest benefits to society through enabling the analysis of anything, by anyone, anywhere. The company has developed a new generation of nanopore-based sensing technology for faster, information rich, accessible and affordable molecular analysis. The first application is DNA/RNA sequencing, and the technology is in development for the analysis of other types of molecules including proteins. The technology is used to understand and characterise the biology of humans and diseases such as cancer, plants, animals, bacteria, viruses, and whole environments. With a thriving culture of ambition and strong innovation goals, Oxford Nanopore is a UK headquartered company with global operations and customers in more than 125 countries. Job Info Job Identification 3101 Job Category Scientific Posting Date 06/24/2026, 02:24 PM Job Schedule Full time Locations Oxford Science Park, OXFORD, OX4 4DQ, GB
26/07/2026
Full time
Work Type & Model: Hybrid - FTC (Maternity Cover) We are looking for a highly motivated individual to join our UK Applications team for maternity cover as a Genomic Applications Manager. This role will be based in Oxford and the successful candidate will lead and manage a proof-of-concept team. About Oxford Nanopore Technologies Oxford Nanopore Technologies is headquartered at the Oxford Science Park outside Oxford, UK, with satellite offices and a commercial presence in many global locations across the US, APAC, and Europe. Our goal is to enable the analysis of any living thing, by anyone, anywhere. We employ individuals from multiple subject areas, including nanopore science, molecular biology and applications, informatics, engineering, electronics, manufacturing, and commercialisation. Our sequencing platform is the only technology that offers real-time analysis, in fully scalable formats from pocket to population scale. This platform can analyze native DNA or RNA and sequence any length of fragment to achieve short to ultra-long read lengths. We aim to inspire anyone to sequence anything, anywhere. Do you want to be part of that? Role Summary Reporting to the Snr. Director, Genomic Applications, the successful candidate will lead and manage a team responsible for delivering proof-of-concept studies across a range of applied market segments. The team will evaluate the performance of nanopore sequencing in new applications, identify technical or workflow gaps, and provide initial solutions or assessments of how these gaps can be addressed. This role will involve designing and overseeing experimental studies, analysing results, and generating high-quality data packages and presentations to support internal decision making and customer engagement. The successful candidate will work closely with cross-functional teams in Oxford to remain aligned with the latest technology developments and to help assess the suitability of emerging nanopore capabilities for new applications and markets. Other responsibilities include Leading and managing a laboratory-based proof-of-concept team within Genomic Applications Designing and executing proof-of-concept studies to evaluate nanopore sequencing performance in new applied market applications Identifying workflow, assay, or technology gaps and proposing potential solutions or development pathways Supporting the assessment and early-stage development of new sequencing applications using ONT's nanopore platform Preparation and QC of sequencing analytes and libraries for experimental studies Analysing and interpreting experimental data, including basic bioinformatic analysis where appropriate Generating clear summaries, reports, and presentation materials to communicate findings to internal stakeholders Collaborating with internal scientific and product development teams to support application evaluation and technology adoption Managing laboratory activities, supporting team development, and assisting junior scientists with experimental and analytical tasks Contributing to the continuous improvement of laboratory workflows, experimental design, and proof-of-concept evaluation processes What We're Looking For We'll expect you to have undertaken successful experimental research from initial concept through to execution and interpretation. This should include experience with DNA and/or RNA manipulation and preferably next-generation sequencing technologies. You will have strong knowledge of molecular biology techniques and sequencing workflows, including sample preparation, library preparation, and quality control methods. Experience in evaluating new technologies, troubleshooting experimental workflows, and identifying practical solutions to technical challenges would be highly advantageous. You should be comfortable working across multiple projects simultaneously and capable of leading and motivating a scientific team in a fast-paced environment. In addition, you will possess excellent communication and problem-solving skills and be able to clearly present scientific findings to a range of audiences. A PhD in molecular biology, genetics, genomics, microbiology, or a related discipline is required, ideally alongside relevant postdoctoral and/or biotechnology industry experience. This role will suit a proactive, organised, and scientifically curious individual with a collaborative approach and the ability to lead effectively in a dynamic environment. Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and abilities to perform the duties of the job. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. About Us Oxford Nanopore Technologies: Our goal is to bring the widest benefits to society through enabling the analysis of anything, by anyone, anywhere. The company has developed a new generation of nanopore-based sensing technology for faster, information rich, accessible and affordable molecular analysis. The first application is DNA/RNA sequencing, and the technology is in development for the analysis of other types of molecules including proteins. The technology is used to understand and characterise the biology of humans and diseases such as cancer, plants, animals, bacteria, viruses, and whole environments. With a thriving culture of ambition and strong innovation goals, Oxford Nanopore is a UK headquartered company with global operations and customers in more than 125 countries. Job Info Job Identification 3101 Job Category Scientific Posting Date 06/24/2026, 02:24 PM Job Schedule Full time Locations Oxford Science Park, OXFORD, OX4 4DQ, GB
Senior Manager Biocompatibility
ConvaTec Inc.
About Convatec Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at risk skin, to improved patient outcomes and reduced care costs. Convatec's revenues in 2024 were over $2 billion. Position Overview The Senior Manager of Biocompatibility leads a team of biocompatibility specialists in delivering biological evaluations in line with ISO 10993 standards or the equivalent from regulated markets globally across our four categories (Ostomy Care, Infusion Care, Advanced Wound Care and Continence Care). The biocompatibility team supports New Product Development (NPD) and Lifecycle Management (LCM) projects, and consults on early stage developments, as well. Biocompatibility is an integrated part of project teams and has a critical role in delivering timely and effectively biological evaluations for new products and in evaluating changes to existing products. The team also partners closely with the Regulatory and Medical/Clinical teams. Fostering effective collaboration is a critical part of the role. The Senior Manager of Biocompatibility is responsible for coaching and developing the team to maintain up to date knowledge of global medical device standards and regulations as well as keep abreast of the state of the art within the field. Key Responsibilities Manage and develop the biocompatibility team - manage and allocate resources in line with project needs and priorities Identify training opportunities for the team towards continuous improvement Ensure seamless and proactive collaboration with the project teams Synthesise a development plan with each team member Ensure the team has up to date knowledge of biocompatibility standards, techniques and protocols Instil a positive working culture of collaboration in line with Convatec's values and leadership behaviors Deliver on biocompatibility for NPD, LCM and research projects Foster cross functional collaboration and teamwork between the biocompatibility team, the business units, project teams, regulatory and clinical teams Lead on accurate project planning and timely execution in partnership with project teams to keep biocompatibility activities visible and integrated into overall project plans Work closely with program/project cross functional teams to provide biocompatibility deliverables in compliance with global regulatory requirements Evaluate and execute biocompatibility studies in support of programs dealing with our medical devices, applying a creative approach to problem solving and detailed knowledge of ISO standard testing Identify, obtain stakeholder buy in and implement continuous process improvements and learning Demonstrate commitment to the Convatec values and lead a culture that implements these values alongside our high performance team principles Address roadblocks by assuming positive intentions of others and take accountability for finding solutions Support biological hazards risk analysis activities Analyse, interpret and draw conclusions from biocompatibility testing, including extractable and leachable chemical characterization and biological evaluations Deliver to company quality metrics (CAPA, NC, IA, etc.) Skills & Experience 10+ years of experience in biocompatibility assessments for NPDs and LCMs in territories including Europe and USA Experience with complex FDA submissions and dealing with FDA queries and feedback is essential 10+ years industrial experience in the field of Medical Device, Pharmaceutical or Biotechnology with expertise in biocompatibility, toxicology, related principles and industry standards Qualifications / Education BSc or higher degree in Biomedical Engineering, Bioengineering, Biology (Biological Sciences), Molecular Cell Biology, Biochemistry, Microbiology or Toxicology Advanced degree (MS or PhD) in these fields preferred Team 6 direct reports. Travel Requirements The position may involve travel around 25% of the time, mostly within Europe but overseas travel is expected. Most trips will include overnight travel. Working Conditions Remote working from home with presence in the office on a weekly or monthly basis driven by business requirements. Special Factors May need to support global discussions in different time zones. Equal Opportunities Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
15/07/2026
Full time
About Convatec Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at risk skin, to improved patient outcomes and reduced care costs. Convatec's revenues in 2024 were over $2 billion. Position Overview The Senior Manager of Biocompatibility leads a team of biocompatibility specialists in delivering biological evaluations in line with ISO 10993 standards or the equivalent from regulated markets globally across our four categories (Ostomy Care, Infusion Care, Advanced Wound Care and Continence Care). The biocompatibility team supports New Product Development (NPD) and Lifecycle Management (LCM) projects, and consults on early stage developments, as well. Biocompatibility is an integrated part of project teams and has a critical role in delivering timely and effectively biological evaluations for new products and in evaluating changes to existing products. The team also partners closely with the Regulatory and Medical/Clinical teams. Fostering effective collaboration is a critical part of the role. The Senior Manager of Biocompatibility is responsible for coaching and developing the team to maintain up to date knowledge of global medical device standards and regulations as well as keep abreast of the state of the art within the field. Key Responsibilities Manage and develop the biocompatibility team - manage and allocate resources in line with project needs and priorities Identify training opportunities for the team towards continuous improvement Ensure seamless and proactive collaboration with the project teams Synthesise a development plan with each team member Ensure the team has up to date knowledge of biocompatibility standards, techniques and protocols Instil a positive working culture of collaboration in line with Convatec's values and leadership behaviors Deliver on biocompatibility for NPD, LCM and research projects Foster cross functional collaboration and teamwork between the biocompatibility team, the business units, project teams, regulatory and clinical teams Lead on accurate project planning and timely execution in partnership with project teams to keep biocompatibility activities visible and integrated into overall project plans Work closely with program/project cross functional teams to provide biocompatibility deliverables in compliance with global regulatory requirements Evaluate and execute biocompatibility studies in support of programs dealing with our medical devices, applying a creative approach to problem solving and detailed knowledge of ISO standard testing Identify, obtain stakeholder buy in and implement continuous process improvements and learning Demonstrate commitment to the Convatec values and lead a culture that implements these values alongside our high performance team principles Address roadblocks by assuming positive intentions of others and take accountability for finding solutions Support biological hazards risk analysis activities Analyse, interpret and draw conclusions from biocompatibility testing, including extractable and leachable chemical characterization and biological evaluations Deliver to company quality metrics (CAPA, NC, IA, etc.) Skills & Experience 10+ years of experience in biocompatibility assessments for NPDs and LCMs in territories including Europe and USA Experience with complex FDA submissions and dealing with FDA queries and feedback is essential 10+ years industrial experience in the field of Medical Device, Pharmaceutical or Biotechnology with expertise in biocompatibility, toxicology, related principles and industry standards Qualifications / Education BSc or higher degree in Biomedical Engineering, Bioengineering, Biology (Biological Sciences), Molecular Cell Biology, Biochemistry, Microbiology or Toxicology Advanced degree (MS or PhD) in these fields preferred Team 6 direct reports. Travel Requirements The position may involve travel around 25% of the time, mostly within Europe but overseas travel is expected. Most trips will include overnight travel. Working Conditions Remote working from home with presence in the office on a weekly or monthly basis driven by business requirements. Special Factors May need to support global discussions in different time zones. Equal Opportunities Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Development - Development Technologist
Finsbury Food Group Hamilton, Lanarkshire
Location: Lightbody, Hamilton Shift: Monday to Friday 8.30am-5.00pm Salary: Competitive We have an exciting opportunity to join the Development team in the role of Development Technologist at our Lightbodysite as part of Finsbury Food Group. With over 135 years of craft baking heritage, Lightbody is proud to be the UK's largest supplier of celebration cakes. From branded favourites like Disney, Mars, Universal and Thorntons to supermarket own label products, we produce over 55 million cakes and sweet treats every year right here in Hamilton. As a Development Technologist, you will be responsible to develop, trial and validate new and existing products in line with agreed customer briefs, commercial targets and factory capability. The role plays a key part in accurate costings, robust documentation, effective risk management and smooth translation from concept through to factory launch, while supporting innovation, food safety, quality and continuous improvement standards. This is what you'll actually do! As a Development Technologist, you will drive innovative product development from concept to launch, ensuring compliance with legal, brand and customer standards. You will work with your cake designers to capture and manage cost effective recipes through our recipe management system, ensuring they are aligned to margin and nutritional targets. You will produce accurate trial documentation and factory handover packs, and be responsible for QAS and arranging customer samples. You will plan and coordinate factory trials, capturing key data, managing risks and delivering clear, evidence based recommendations. Working closely with Technical and cross functional teams, you will support product validation including shelf life, microbiological and physical testing. You will benchmark products against the market, identify opportunities for improvement and contribute to continuous innovation and process excellence. Flexibility in working hours is required to support factory trials and launch activities. Ideally this is you! Essential Qualifications and Experience Degree preferred in Food Science / Technology / Process Engineering or similar; or HND equivalent or relevant experience Strong understanding of product development processes from concept to launch Knowledge of factory processes and manufacturability considerations Experience generating recipes, costings and managing BoMs Ability to manage multiple projects to critical path deadlines Strong analytical skills with ability to interpret trial and validation data Knowledge of food safety, microbiology and shelf life validation Commercial awareness and understanding of margin targets Strong communication and stakeholder management skills Passion for food innovation and emerging market trends Detail oriented, organised and solutions focused Valid UK driving licence preferred What's in it for you! Enhanced maternity & paternity leave to allow quality time with your new arrival Enhanced pension scheme for employees Death in service benefit Free employee assistance programme (open to colleagues and their families) Retail discounts accessible via our benefits hub platform Refer a friend scheme (up to £300 per referral - terms & conditions dependent) Employee recognition awards Extensive learning & development opportunities (including opportunities for sponsored professional memberships and our own in house development course) Opportunity to be part of a fantastic, growing organisation Are you the perfect fit for Development - Development Technologist? Get in touch to learn more.
04/07/2026
Full time
Location: Lightbody, Hamilton Shift: Monday to Friday 8.30am-5.00pm Salary: Competitive We have an exciting opportunity to join the Development team in the role of Development Technologist at our Lightbodysite as part of Finsbury Food Group. With over 135 years of craft baking heritage, Lightbody is proud to be the UK's largest supplier of celebration cakes. From branded favourites like Disney, Mars, Universal and Thorntons to supermarket own label products, we produce over 55 million cakes and sweet treats every year right here in Hamilton. As a Development Technologist, you will be responsible to develop, trial and validate new and existing products in line with agreed customer briefs, commercial targets and factory capability. The role plays a key part in accurate costings, robust documentation, effective risk management and smooth translation from concept through to factory launch, while supporting innovation, food safety, quality and continuous improvement standards. This is what you'll actually do! As a Development Technologist, you will drive innovative product development from concept to launch, ensuring compliance with legal, brand and customer standards. You will work with your cake designers to capture and manage cost effective recipes through our recipe management system, ensuring they are aligned to margin and nutritional targets. You will produce accurate trial documentation and factory handover packs, and be responsible for QAS and arranging customer samples. You will plan and coordinate factory trials, capturing key data, managing risks and delivering clear, evidence based recommendations. Working closely with Technical and cross functional teams, you will support product validation including shelf life, microbiological and physical testing. You will benchmark products against the market, identify opportunities for improvement and contribute to continuous innovation and process excellence. Flexibility in working hours is required to support factory trials and launch activities. Ideally this is you! Essential Qualifications and Experience Degree preferred in Food Science / Technology / Process Engineering or similar; or HND equivalent or relevant experience Strong understanding of product development processes from concept to launch Knowledge of factory processes and manufacturability considerations Experience generating recipes, costings and managing BoMs Ability to manage multiple projects to critical path deadlines Strong analytical skills with ability to interpret trial and validation data Knowledge of food safety, microbiology and shelf life validation Commercial awareness and understanding of margin targets Strong communication and stakeholder management skills Passion for food innovation and emerging market trends Detail oriented, organised and solutions focused Valid UK driving licence preferred What's in it for you! Enhanced maternity & paternity leave to allow quality time with your new arrival Enhanced pension scheme for employees Death in service benefit Free employee assistance programme (open to colleagues and their families) Retail discounts accessible via our benefits hub platform Refer a friend scheme (up to £300 per referral - terms & conditions dependent) Employee recognition awards Extensive learning & development opportunities (including opportunities for sponsored professional memberships and our own in house development course) Opportunity to be part of a fantastic, growing organisation Are you the perfect fit for Development - Development Technologist? Get in touch to learn more.

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