Industrial engineer jobs in OxfordCrear alertas

iotaSciences, a University of Oxford spin-out, is an innovative and fast-growing biotechnology company that emerged from the University’s engineering and biology departments. We offer unique solutions to cell line development. These solutions accelerate and advance biomedicine across a wide range of applications including gene editing, disease modelling and drug discovery; with current customers from universities, hospitals and industry. Our employees are motivated to deliver the most innovative next generation technologies in biomedicine that will ultimately translate ideas to clinics faster. Senior Research Engineer About the role As a Research Engineer at iotaSciences, you'll be at the forefront of developing the next generation of fluid handling and automated microscopy robots. This is a hands-on, NPI-focused role where your primary responsibility will be designing and implementing computer vision models for image recognition in cell biology. You will also: • Collaborate with software engineers to integrate computer vision models into a Windows-based microscopy application., • Develop programs for a microfluidic robot, programming robotic motions., • Design and run experiments to gather empirical data, perform data analysis and assess robotic performance. We're looking for a highly motivated and independent individual with a strong background in engineering or a similar technical field. You should have previous experience in a research or product development environment, whether academic or industrial. You should be able to comfortable being the technical authority on NPI projects and have experience taking a project from concept to release. This role requires a candidate who can work across multiple disciplines, collaborating closely with software, biology, and hardware teams. The primary goal is to develop intelligent systems that accelerate biomedicine by testing concepts and finding innovative solutions to complex problems. As a member of a small company, your day-to-day activities will be highly varied, and you'll be expected to participate in wider company projects as needed. This provides a unique opportunity to gain experience across various departments and expand your skill set. Requirements (essential) • Degree in engineering, physics, computer science, or a related field. Advanced degrees preferred., • Strong experience in computer vision (PyTorch, TensorFlow, OpenCV)., • Proficiency in Python, • Experience using version control (e.g. Git)., • Ability to design and conduct experiments., • Strong communication skills., • Willingness to participate in wider company projects when needed., • Experience of technical leadership on projects. Desirable experience (not all are needed) • Familiarity with Windows app development in C#/VB.NET., • Exposure to multi axis motion control programming (e.g. g-code)., • Foundation in fluid dynamics., • C++ firmware experience., • Mentoring for more junior R&D engineers.

Software Automation Engineer Do you want to help build the next generation of autonomous lab platforms? This role focuses on creating the automation backbone behind next-generation lab and robotics platforms. You’ll work at the intersection of instruments, robots, firmware, and software - building the integrations and workflows that enable true autonomous experimentation. Expect a mix of device-level engineering, system-wide architecture, and hands-on problem solving. If you enjoy connecting hardware, software, and clever engineering to build systems that run themselves, you’ll fit right in. What You’ll Be Doing: • Developing automated workflows that turn complex experimental steps into structured, repeatable software protocols using robotics, • Integrate lab hardware and software, exposing firmware capabilities through clean, standard interfaces., • Contribute to system architecture design to ensure high reliability, monitoring, and performance across all automation platforms., • Break systems down, understand them deeply, and reimagine how they can be used to create innovative solutions., • Collaborate with scientific, technical, and operational colleagues to ensure automation meets real-world needs., • Evaluate new tools and technologies with external vendors and integrate them into existing workflows. What We’re Looking For: • Experience in automation engineering, robotics, biotech, or industrial systems integration., • Proven track record of designing and deploying robust automation systems, including multi-device orchestration., • Skilled in firmware-level control, driver development, and exposing device capabilities through APIs., • Strong programming skills in Python and C/C++., • Experienced in software best practices: version control, PR reviews, documentation, and efficient workflows., • A creative thinker - able to design automation that goes beyond simply replicating human tasks. Nice to Have: • Relevant degree in Engineering, Computer Science, Robotics, or similar., • Familiarity with open-source automation libraries, such as PyLabRobot., • Experience creating digital twins or virtual representations of lab devices., • Background in biotech, pharma, materials science, or other R&D areas that rely heavily on automation. Offices and Lab located in Oxford. Hybrid working c.3 days in office Competitive salary + benefits dependent on experience. Ready to help build the next generation of intelligent robots? Apply now and join a fast-moving team shaping the future of applied robotics and AI.

Fire &/or Security / Fire Alarm Engineer (Service or Installation) Salary: £28,000–£40,000 per year (DOE) Locations: Work across commercial, residential, and industrial sites Roles: Service and Installation opportunities If you’re a skilled Fire & Security Engineer or a Fir

Our client, a leading global HVAC company is looking for a Refrigeration Engineer with a solid background in the commercial or industrial refrigeration industry to join their fantastic team.On offer: Competitive base salary of up to £48,000 per annum with an OTE of £60,000+.Including com

Industrial Refrigeration Engineer.A specialist in bespoke refrigeration and temperature-controlled solutions, this company designs, installs, and maintains complex systems for commercial and industrial applications, including food processing, cold storage, and manufacturing environments.Known for de

Are you a Chemical Process Engineer from an oil and gas, industrial or petrochemical background looking for a role where you can work on high value projects and shape advanced technology that supports a circular economy?. Process Engineer - Chemical and Recycling. You will join a growing organisatio

Development of real-time machine control software in C#/.NET, integrating lasers, motion control, robotics, and industrial systems.Were looking for a Software Software Engineer to help build and maintain high-performance software for advanced industrial systems.NET software (operator tools + backend

Senior Software Controls Engineer Location: Oxford Salary: Ranging from £50-£70k This is a unique role focusing on the development of real-time machine control software in C#/.NET, integrating lasers, motion control, robotics, and industrial systems.The Role * Build and maintain C#/.

Area Sales Manager / Sales Engineer / Business Development Manager required to join a UK leading Compressor Sale & Service Provider. The successful Area Sales Manager / Sales Engineer / Business Development Manager will work hybrid, responsible for new business development and key account management covering Oxford, Watford, and surrounding areas.selling compressed air equipment such as compressors, nitrogen generators, blowers and dryers and associated equipment. The Area Sales Manager / Sales Engineer / Business Development Managermust have experience selling engineered products and solutions in to end user channels . Full product training provided. Area Sales Manager / Sales Engineer / Business Development Manager Package £40,000-£50,000 plus a high OTE Company car or allowance 25 days holiday plus bank holidays Phone, Laptop, plus additional benefits Continued professional development Area Sales Manager / Sales Engineer / Business Development Manager Role Managing a number of key accounts for compressed air equipment such as compressors, nitrogen generators, blowers and dryers and associated equipment. Manage and grow existing relationships as well as business development, selling compressed air products and solutions. Maintaining new compressor sales with demonstration, exhibition, and negotiation to achieve targets. Working closely with the compressed air Service Department to ensure an excellent standard of after-sales service is provided. Liaise with various engineering departments. Work hybrid, covering Oxford, Watford, and surrounding areas. Area Sales Manager / Sales Engineer / Business Development Manager Requirements Experience as a Key Account Manager, Account Manager, Area Sales Manager, Sales Engineer, Business Development Manager, Technical Sales Engineer, Sales Representative or similar within engineering. Compressor Service Engineers looking to come off the tools and progress into a sales role would also be of interest. Experience selling engineering products such as compressors, vacuum systems, filtration, blowers & dryers, downstream equipment, refrigeration, nitrogen generators or similar compressed airrelated products / services is advantageous. Experience selling transferable products such as pumps, valves, plant equipment, pneumatics, medical gas, hydraulics, rotating equipment, MRO, industrial systems or similar. A technical engineering qualification, Apprentice trained, HNC, HND or Degree would be advantageous. Full clean driving license. Willingness toWork hybrid, covering Oxford, Watford, and surrounding areas. TPBN1_UKTJ

Due to their consistent growth and expansion, they're now looking for a Industrial Door Engineer based in Hampshire to join them ASAP!. They're looking for an experienced Industrial Door Engineer to service, repair and install all types of industrial and automatic door equipment predominantly within

Field Service Engineer - Pumps Location: Oxford – M4 Corridor Salary - Up to £45,000 basic salary The Company A leading supplier specialising in Submersible and Industrial pumps, an opportunity to join a company who have been established for 40 years.Employees are at the heart of the b

Company description: OXB is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world.Read all the information about this opportunity carefully, then use the application button below to send your CV and application.One of the original pioneers in cell and gene therapy, OXB has more than 30 years of experience in viral vectors, the driving force behind the majority of gene therapies.Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells.One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells.This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy).OXB collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors.OXBs world-class capabilities span from early-stage development to commercialisation.These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise.Job description: Join Us in Changing Lives At OXB , our people are at the heart of everything we do.Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful .Were currently recruiting for a Head of Validation .In this role, you willbe accountable for OXB UK qualification / re-qualification / validation activities of its GxP facilities / equipment / systems and processes.Develops the Validation functions capability and strategic direction as well as leading the team to ensure that the appropriate regulatory, quality and service level requirements are delivered in a robust, science and risk-based approach., playing a key part in advancing our mission and making a real difference.Your responsibilities in this role would be: Defining the strategic direction of the Validation function with the Site Leadership Team.Accountable for leading the Validation function; building the team and capabilities, establishing a clear vision, setting and managing departmental budget, coaching, mentoring, recruitment, training and performance management.Ensures that OXBs GxP facilities, equipment, systems, including computer systems, & processes are qualified and validated in accordance with the relevant regulatory requirements of the countries/markets in which the business operates.Works collaboratively across the business to ensure that Validation-related processes and procedures are well-represented in OXB/strategic partner product programmes, regulatory submissions and in all CMC responses to regulatory agencies.Drive a science and risk-based strategy to ensure the right level of qualification and validation are achieved in a compliant way.Engages with OXBs strategic partners and collaborators in promoting the Companys qualification/re-qualification/validation activities and to reinforce OXBs credibility.Proposes functional strategy/tactics/performance to the senior management internally.Regularly presents strategic and performance information and influences the leadership team on validation technical and regulatory considerations.Actively works with internal/external team members to define and agree the most appropriate functional strategy/tactics for qualification/validation of OXBs client programs.Ensures validation master plans (VMPs), programs of work, protocols and procedures are established which facilitate the delivery of qualification/re-qualification/validation activities to the required quality and regulatory standards.Manages the qualification/requalification/validation deliverables to meet third party/client and user/system-owner schedule/timeline requirements.Leads and empowers the Validation team in identifying, assessing and adopting (as appropriate) validation/ qualification process improvements and better ways of working.Maintains an active awareness of developments in regulatory standards and industry best practices which may impact the qualification and validation requirements.We are Looking For: Degree in Science / Engineering or similar Strong technical and regulatory knowledge of validation/ qualification requirements associated with facilities, equipment and systems, bulk manufacturing, fill-finish, sterilisation, sanitisation/cleaning and cold-chain distribution gained within a biopharmaceuticals or relevant pharmaceuticals industrial environment.Knowledge and understanding of Environmental, Health & Safety (EHS) requirements as they impact the Validation function and associated activities.A strong track record of establishing validation master plans (VMPs), protocols and procedures which facilitate the delivery of qualification/validation activities to the required quality and regulatory standards.Knowledgeable of GxP, CMC, ICH and compendial (USP/EP/JP) regulatory requirements.Knowledge of relevant regulatory agency guidance including ICH, FDA, EMA, and authorities in other major geographic areas is essential About Us: OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world.One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies.OXB collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors.OXBs world-class capabilities span from early-stage development to commercialisation.These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.Why Join Us? ??Competitive total reward packages ??Wellbeing programmesthat support your mental and physical health ??Career development opportunitiesto help you grow and thrive ??Supportive, inclusive, and collaborative culture ??State-of-the-art labs and manufacturing facilities ?? A company that lives its values: Responsible, Responsive, Resilient, Respect We want you to feel inspired every day.At OXB, were future-focused and growing fast.We succeed togetherthrough passion, commitment, and teamwork.Ready to Make a Difference? Collaborate.Contribute.Change lives.We offer: Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world.One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies.Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells.One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells.This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy).Oxford Biomedica collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors.Oxford Biomedicas world-class capabilities span from early-stage development to commercialisation. xjlbheb These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise.

Company description: Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy). Oxford Biomedica collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. Oxford Biomedica's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise. Job description: Join Us in Changing Lives At OXB , our people are at the heart of everything we do. Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful . Were currently recruiting for a Senior Maintenance Engineer for the Engineering team. In this role, you will utilize Good Engineering Practices (GEP) to establish and maintain the industrial process automation, building automation and operational technology systems required to support cGMP manufacturing and process development. As a system owner, you will be responsible for day-to-day operations support and troubleshooting, project execution, commissioning and qualification support, and optimizing process and utilities equipment within a regulated cGMP facility, playing a key part in advancing our mission and making a real difference. Your responsibilities in this role would be: Assuming ownership responsibility of control systems and other operational technologies by applying the engineering lifecycle to enable cGMP manufacturing. Organizing and leading all aspects of cross-functional internal projects including scope, schedules, and execution. Applying technical expertise in ensuring the reliability of complex process equipment, data, and building and utilities systems. Developing solutions and best practices for a variety of problems with moderate scope and complexity, and working collaboratively with Quality, Manufacturing, Facilities, Process Development, external supply partners, and vendors. Responding to support calls and troubleshoots equipment and uses evaluation, judgement, and interpretation to resolve issues and select best course of action. Being a Control Systems Engineering representative for capital projects involving building automation, process and utilities equipment for cGMP facilities. We are looking for: Technical/ Complex equipment systems Control systems. Bioreactor/ Filling line background. Background in GMP/ Pharma/ regulated environments: Bachelor's degree in Electrical Engineering / Computer Science / Chemical Engineering or equivalent, with a minimum of 5 years of experience in a cGMP engineering environment, or advanced degree in lieu of experience. Significant knowledge and understanding of GMP engineering principles and practices in the gene therapy industry. Manufacturing control systems automation background focused specifically in the design, installation, programming, validation, and in lifecycle maintenance of automated equipment, specifically in a GMP environment. Knowledge of GAMP software development lifecycle, ANSI/ISA-S88 and S95 industry standards, and 21 CFR Part 11. Demonstrated experience with network architecture including TCP/IP, Routing, Switching, Network IDS/IPS, Active Directory, Domain Integration, and Firewalls. Able to accommodate changing priorities and deadlines and work independently solving complex process and equipment problems. About Us: OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 25 years of experience in viral vectors; the driving force behind the majority of gene therapies. OXB collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXBs world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise. Why Join Us? ??Competitive total reward packages ??Wellbeing programmesthat support your mental and physical health ??Career development opportunitiesto help you grow and thrive ??Supportive, inclusive, and collaborative culture ??State-of-the-art labs and manufacturing facilities ?? A company that lives its values: Responsible, Responsive, Resilient, Respect We want you to feel inspired every day. At OXB, were future-focused and growing fast. We succeed togetherthrough passion, commitment, and teamwork. Ready to Make a Difference? Collaborate. Contribute. Change lives. We offer: Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy). Oxford Biomedica collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. Oxford Biomedica's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise. TPBN1_UKTJ

Company description: OXB is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, OXB has more than 30 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy). OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise. Job description: Join Us in Changing Lives At OXB , our people are at the heart of everything we do. Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful . Were currently recruiting for a Head of Validation . In this role, you willbe accountable for OXB UK qualification / re-qualification / validation activities of its GxP facilities / equipment / systems and processes. Develops the Validation functions capability and strategic direction as well as leading the team to ensure that the appropriate regulatory, quality and service level requirements are delivered in a robust, science and risk-based approach., playing a key part in advancing our mission and making a real difference. Your responsibilities in this role would be: Defining the strategic direction of the Validation function with the Site Leadership Team. Accountable for leading the Validation function; building the team and capabilities, establishing a clear vision, setting and managing departmental budget, coaching, mentoring, recruitment, training and performance management. Ensures that OXBs GxP facilities, equipment, systems, including computer systems, & processes are qualified and validated in accordance with the relevant regulatory requirements of the countries/markets in which the business operates. Works collaboratively across the business to ensure that Validation-related processes and procedures are well-represented in OXB/strategic partner product programmes, regulatory submissions and in all CMC responses to regulatory agencies. Drive a science and risk-based strategy to ensure the right level of qualification and validation are achieved in a compliant way. Engages with OXBs strategic partners and collaborators in promoting the Companys qualification/re-qualification/validation activities and to reinforce OXBs credibility. Proposes functional strategy/tactics/performance to the senior management internally. Regularly presents strategic and performance information and influences the leadership team on validation technical and regulatory considerations. Actively works with internal/external team members to define and agree the most appropriate functional strategy/tactics for qualification/validation of OXBs client programs. Ensures validation master plans (VMPs), programs of work, protocols and procedures are established which facilitate the delivery of qualification/re-qualification/validation activities to the required quality and regulatory standards. Manages the qualification/requalification/validation deliverables to meet third party/client and user/system-owner schedule/timeline requirements. Leads and empowers the Validation team in identifying, assessing and adopting (as appropriate) validation/ qualification process improvements and better ways of working. Maintains an active awareness of developments in regulatory standards and industry best practices which may impact the qualification and validation requirements. We are Looking For: Degree in Science / Engineering or similar Strong technical and regulatory knowledge of validation/ qualification requirements associated with facilities, equipment and systems, bulk manufacturing, fill-finish, sterilisation, sanitisation/cleaning and cold-chain distribution gained within a biopharmaceuticals or relevant pharmaceuticals industrial environment. Knowledge and understanding of Environmental, Health & Safety (EHS) requirements as they impact the Validation function and associated activities. A strong track record of establishing validation master plans (VMPs), protocols and procedures which facilitate the delivery of qualification/validation activities to the required quality and regulatory standards. Knowledgeable of GxP, CMC, ICH and compendial (USP/EP/JP) regulatory requirements. Knowledge of relevant regulatory agency guidance including ICH, FDA, EMA, and authorities in other major geographic areas is essential About Us: OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies. OXB collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXBs world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise. Why Join Us? ??Competitive total reward packages ??Wellbeing programmesthat support your mental and physical health ??Career development opportunitiesto help you grow and thrive ??Supportive, inclusive, and collaborative culture ??State-of-the-art labs and manufacturing facilities ?? A company that lives its values: Responsible, Responsive, Resilient, Respect We want you to feel inspired every day. At OXB, were future-focused and growing fast. We succeed togetherthrough passion, commitment, and teamwork. Ready to Make a Difference? Collaborate. Contribute. Change lives. We offer: Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy). Oxford Biomedica collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. Oxford Biomedica's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise. TPBN1_UKTJ

Senior EC&I Engineer Permanent Main Purpose of Job: Definition and distribution of the scope of work to ensure that all work is executed safely, on time and at appropriate levels of quality. Delivery of all design and engineering to meet the requirements of Design Reviews and HAZOPs within Project procedures. Supervision of less experienced engineering employees, engineering resource management and interviews. Position in Organisation: • Reporting to Principal Engineers with ultimate line management responsibilities being with the Chief Engineer within your discipline, • Reports to Principal Engineer, Team Leader or Department Manager, • Normally supervises a design or project team of up to 5 engineering staff, although the team may be supplemented by staff from elsewhere., • Responsible for the allocation of work and managing quality, progress and cost of the work carried out within the project, • Responsible for managing project subcontracts, • Regularly interacts with clients and managers of other engineering disciplines, • Responsible for communications within project team on your allotment of the project Key Accountabilities: • Design, Specification, Procurement, Supply/Manufacture Liaison, Installation, Acceptance Testing, Commissioning and Operator Training in Nuclear Engineering Projects, • Liaison with multi disciplines, • Technical Consultancy, • Project Management including quality, progress and cost control including documentation, • Sales Support and Customer care, • Manage Contractors and Sub Contractors, Staff Development, • Manage safety by developing and reinforcing the safety culture, compliance with safety regulations (eg. CDM and CE marking), and the application of safety systems Experience and attributes required for the role: Essential: • Degree qualified in a relevant technical / engineering discipline or demonstrable experience, • A full UK driver’s licence, • Working towards Chartered Engineer status (where applicable), • Minimum 5 years’ experience in the Nuclear industry, • Understanding of design requirements to support nuclear safety cases, • Experience of managing sub-contracts, • Knowledge of safety regulations including CDM, • Experience of checking design documentation including drawings and supporting calculations, • Experience and/or ability of leading a technical team within a professional project delivery environment, • Organisation & Collaborations skills, • Demonstrable expertise in working to tight deadlines, • Quality & service driven attitude Desirable: • Chartered Engineer and candidates nearing chartership are preferred. Membership to appropriate institutions is preferred e.g. IET, • EC&I design integration with control systems (PLC/SCADA) would be advantageous., • Experience of Design Substantiation to support safety cases including assessment of new and existing systems., • Additional experience obtained within the Defence sector would be advantageous., • Experience of bid preparation Subsidiary of VINCI Construction, and division of the world-leading VINCI Group, NUVIA is an international company that operates world-wide on highly regulated and sensitive industrial sites, and has done for decades. We have been involved in all the major nuclear projects in the world thanks to our solid and historical expertise.

Up to £45k (depending on experience).This is an exciting opportunity to join an established engineering consultancy seeking an Automation Engineer to deliver high-quality automation and control engineering services across industrial sectors.The position offers a varied and hands-on opportunity with

Development of real-time machine control software in C#/.NET, integrating lasers, motion control, robotics, and industrial systems.Were looking for a Software Software Engineer to help build and maintain high-performance software for advanced industrial systems.

Senior Electrical and Controls Design Engineer - Industrial Automation Location: South Oxfordshire Salary: £55,000-£60,000 + Benefits A leading advanced engineering company at the forefront of automation and inspection systems is seeking a Senior Electrical and Controls Design Engineer to join its growing team. Working with blue-chip manufacturers across automotive, medical, electronics and high-tech...

Process Design Engineer (CAD & Projects) £36,000 - £38,000 + Training + Progression + Benefits Banbury (Commutable from Bicester, Oxford, Northampton, Rugby, Witney, Leamington Spa and surrounding areas) Do you have strong AutoCAD skills and experience designing industrial layouts, plant systems, or process-driven projects? Are you looking for a role where your designs directly influence how large-sc...

A technology solutions company based in Oxford is looking for a skilled Software Engineer to design sophisticated C# applications for industrial control systems.

Senior Magnet Design Engineer role at UK Industrial Fusion Solutions (UKIFS) Ltd, a subsidiary of UK Atomic Energy Authority (UKAEA). The role reports to the STEP Magnets Engineering Manager and involves collaboration with international partners, industry, and academic collaborators. BEng or BSc in

We are recruiting on behalf of a global manufacturer of forklift trucks and warehouse equipment who is seeking skilled Resident Engineers to join their team.Please read the information in this job post thoroughly to understand exactly what is expected of potential candidates.As a Resident Engineer, youll work on-site at one of our customer locations, becoming an integral part of their team while handling a wide variety of technical tasks.Every day presents new challenges and opportunities to develop your skills in the dynamic world of material handling.Benefits include: Competitive salary based on experience Monday to Sunday working week with shift premiums and overtime available 33 days annual leave including statutory bank holidays, plus additional days for long service Company pension scheme with employer contribution Employee discount and incentive schemes Full induction and world-class technical training Long-term career development and progression opportunities Full forklift licence provided Laptop, phone, specialist tools, and PPE supplied Role & Responsibilities: Diagnose and resolve technical issues, ensuring customer equipment operates efficiently Conduct preventative maintenance checks Provide on-site technical support and build strong customer relationships Maintain high standards for safety, performance, and customer satisfaction Ideal Candidate: Experience as a vehicle technician, mechanical engineer, forklift technician, plant fitter, plant technician, or similar role Experience with plant equipment, powered access, agricultural machinery, motor vehicles, xjlbheb or industrial cleaners is desirable NVQ Level 3 (or equivalent) preferred but not essential Comfortable using IT equipment for record-keeping and ordering Full UK driving licence Ability to work independently and as part of a team If youre looking for a hands-on role with excellent training, development, and progression in the material handling industry, this is the opportunity for you.Please apply today or contact Oliver Cole @ Smart Search Technical

Company description: Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies. Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patients cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy). Oxford Biomedica collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. Oxford Biomedica's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise. Job description: Join Us in Changing Lives At OXB , our people are at the heart of everything we do. Were on a mission to enable life-changing therapies to reach patients around the worldand were looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful . Were currently recruiting for a Manufacturing Equipment & Systems Specialist to join our Manufacturing Team . In this role, you willensure compliance of GMP Equipment & Systems within the manufacturing department enabling efficient batch delivery against production schedule in line with GMP, safety and environmental requirements, playing a key part in advancing our mission and making a real difference. Please note that this role is an onsite opportunity. Your responsibilities in this role would be: Generating and reviewing of periodic Asset documentation including audit trails, Asset Folders, and User Access levels Maintaining access control for manufacturing and ensuring trained personnel and host access to support Validation / Engineering activities Supporting in progressing of Validation Lifecycle documents and activities for assets (URS, DQ, RQ, VRRs, CST etc) Generating and updating of asset documentation e.g. equipment logbooks, SOPs Providing technical support and point of contact for queries / data from internal departments e.g. Validation and support QMS, and Audits and Client requests Liaising with Equipment & Systems vendors to resolve any technical issues that are identified Executing NPI actions which relate to equipment introduction or modification Supporting the implementation and review of HAZOPs Acting as the subject matter expert where required for QMS and supporting/taking ownership of QMS records for equipment and Systems We are Looking For: A-Level, preferably science based with previous industrial experience Graduate in STEM subject (preferred) Experience working in a GMP environment Experience working with of Cell & Gene therapy manufacturing equipment and systems. e.g. bioreactors, chromatography, clean rooms etc. Ability to travel across all Oxfordshire sites Willingness to working within Cleanroom environment when required About Us: OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 25 years of experience in viral vectors; the driving force behind the majority of gene therapies. OXB collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXBs world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise. Why Join Us? Competitive total reward packages Wellbeing programmesthat support your mental and physical health Career development opportunitiesto help you grow and thrive Supportive, inclusive, and collaborative culture State-of-the-art labs and manufacturing facilities A company that lives its values: Responsible, Responsive, Resilient, Respect We want you to feel inspired every day. At OXB, were future-focused and growing fast. We succeed togetherthrough passion, commitment, and teamwork. Ready to Make a Difference? Collaborate. Contribute. Change lives. TPBN1_UKTJ

Proven knowledge of the Industrial Refrigeration engineering services sector, and the expectations of Industrial Refrigeration customers. We currently seeking an experienced Industrial & Commercial Refrigeration Service Engineer to cover Various customer locations throughout the East Midlands & Linc

They're looking for an experienced Industrial Door Engineer to service, repair and install all types of industrial and automatic door equipment predominantly within Hampshire. Due to their consistent growth and expansion, they're now looking for a Industrial Door Engineer based in Hampshire to join

Industrial Refrigeration Engineer. A specialist in bespoke refrigeration and temperature-controlled solutions, this company designs, installs, and maintains complex systems for commercial and industrial applications, including food processing, cold storage, and manufacturing environments. Experience

They're looking for an experienced Industrial Door Engineer to service, repair and install all types of industrial and automatic door equipment predominantly within Hampshire. Due to their consistent growth and expansion, they're now looking for a Industrial Door Engineer based in Hampshire to join

Industrial Door Engineer - Devon Industrial Door Engineer Devon £16 - £21 per hour depending on experience Overtime rates at 1. Annual bonus An up-and-coming industrial door maintenance specialist is currently looking to bolster its engineering team and is targeting an additional En

Mechanical Engineer Pipework / Building Services. This role is ideal for an engineer with a strong background in. Mechanical engineer with strong.

Industry Sector: Service Engineer, Maintenance Engineer, Engineer, Industrial Doors, Steel Doors, High-Speed Doors, Roller Shutters, Sectional Doors, Loading Bays, Dock Levellers, Dock Shelters, Buffers, Automatic Doors, Entrance Systems, Automatic Entrance Systems, BSEN16005, BS EN 16005. Industria

Job Title: Service Engineer Location: Heathrow Airport Employment Type: Permanent Salary: £36,000 – £40,000 About the Role We are seeking an experienced Service Engineer to join an experienced team at Heathrow Airport. Key Responsibilities * Install, commission, and maintain m

Fire Suppression / Sprinkler Engineer. Fire Suppression / Sprinkler Engineer. This is a fantastic opportunity for an engineer with strong sprinkler or riser experience whos looking for a stable, well-paid role with long-term progression.

Industrial Electrical Engineer / Electrician (Training into COMPEX). Are you an Industrial Electrical Engineer, Electrician or similar looking to be heavily invested in through highly technical training such as COMPEX, increase your earnings through door to door overtime and further progress your ca

The Role:Candidates would carry out the service and maintenance of Industrial Refrigeration systems and associated plant on customer sites throughout Staffordshire and the Nor.

Industrial Refrigeration Engineer. A specialist in bespoke refrigeration and temperature-controlled solutions, this company designs, installs, and maintains complex systems for commercial and industrial applications, including food processing, cold storage, and manufacturing environments. Experience

OTE:£42,900 £50,050 (including overtime and standby)Basic Salary:£39,000 £45,500 (including basic and paid travel time, dependent on experience)Benefits includeProfit-related bonus30 days holiday (22 days + 8 bank holidays)Door-to-door paid travelSubsidised healthcare schemeCompany pension sch

Generator / Yard EngineerLocation:Bristol (Warmley area)Salary:£30,415 £38,300 (dependent on experience)Hours:Full-Time, PermanentAbout the RolePertemps are delighted to be recruiting on behalf of a leading power solutions specialist for an on-site Generator / Yard Engineer to join their Bristol

What you will doOur Industrial Refrigeration (IREF) division delivers project, maintenance, and service solutions supporting manufacturing, cold storage, and R&D testing. As the OEM for SABROE, Frick Compressors, and York products, we provide nationwide service with highly trained engineers offering

A leading European manufacturer of loading bays, dock levellers, and industrial door systems is looking for an Industrial Door Engineer to join their expanding team in the Slough and Crawley areas. The role involves servicing, repairing, and fault-finding on industrial doors, dock levellers, and rel

Overview We are seeking a dedicated Industrial Door Service Engineer to join our team. The successful candidate will be responsible for maintaining and repairing a wide range of industrial doors across various sites.

The Person: Service Engineer Industrial, manufacturing, waste or similar background Reference number BBBH23290a Engineer, Engineering, Servicing, Repairing, Commissioning, Mechanical, Hydraulics, Waste, Field, Local, Electric, Electrical, Industrial, Manufacturing, Machinery, Bedford, Northampton, L

Industrial Refrigeration EngineerCambridgeshire£45,000 - £50,000 per annum A specialist in bespoke refrigeration and temperature-controlled solutions, this company designs, installs, and maintains complex systems for commercial and industrial applications, including food processing, cold storage,

Industrial Refrigeration Engineer - Ammonia Refrigeration - South East - Up to £54,000 basic, OTE £70,000 plus About the Company We are looking for Industrial Refrigeration Engineers to work on properties across the South East of the UK, working as part of a team for a well established Industri

Industrial Refrigeration Engineer - Central Belt - to £52k. This role involves service, maintenance and troubleshooting of industrial and commercial refrigeration systems across sites such as: Low temperature food distribution centresChill temperature.

An excellent opportunity for an experienced Industrial Door Engineer (Industrial & Automatic Doors) to join a well-established company!Job Type: Full-Time, Permanent.

Role: Fire Suppression / Sprinkler Engineer Salary: £50,000 £56,000 + packageLocation: East London Were recruiting for an experienced Fire Suppression / Sprinkler Engineer to join a growing team within a leading building services provider. This is a fantastic opportunity for an engineer with stro

Lead Engineer (Industrial Doors/Roller Shutters)Colchester, Essex £30,000 - £40,000 + Training + Progression + Overtime + PensionAre you a Lead Engineer or similar, coming from a background within the Industrial Door industry, specifically with previous working experience on Roller Shutters, looki

Industrial Door Engineer BristolSalary:£36,000 - £42,000 + Overtime + Van + BenefitsLocation:Bristol & Surrounding AreasWe are currently seeking an experiencedIndustrial Door Engineerto join a leading specialist in the installation, maintenance and repair of industrial doors, shutters and loading