Job Title : Rolling Stock Overhaul Technician Overview: You will be based in Manchester, joining a team of over 80 professionals working on a major rolling stock overhaul project for the Class 390 Avanti High Speed Trains. This is an excellent opportunity to be part of a world-leading organisation responsible for maintaining and ensuring the reliability of this iconic, globally recognised fleet. Rullion has a strong long-standing partnership with our client and we place great importance on contractor welfare. Your well being is our priority, with an experienced on-site account manager available to support you throughout the project. This role not only offers an enjoyable working environment, but also the chance to develop valuable skills to progress further in your career. Purpose of Role: You will be working as part of the overhaul team to service, maintain, repair and overhaul rolling stock and equipment, including the latest generation in train technology to laid down Vehicle Maintenance Instructions Ensuring all Overhaul activities are carried out in a safe, efficient and cost-effective manner, whilst constantly seeking to improve quality. Location: Manchester Train Care Centre, Longsight, M12 4HR Start Date: Start of Project = staggered starts each week from 05/01/2026 up to 23/02/2026 Envisaged End Date: End of June 2027 Shift Pattern: Days and Nights on a 2 week shift rotation ( This will take effect once project is in full operation ) Hours: 40 hours on ramp up - 48 hours per week once project is in full operation Start and Finish times: ( Subject to change at client's request ) Days : 07:00 hours to 18:00 hours / 07:00 hours to 15:00 hours Nights : 19:00 hours to 06:00 hours / 20:00 hours to 07:00 hours Overhaul Technician - Pre Tech competency Pre 12 weeks: PAYE 27.41 per hour (28 days accrued leave) / Umbrella 35.47 per hour Post 12 weeks: PAYE 29.53 per hour (33 days accrued leave) / Umbrella 40.32 per hour Overhaul Technician - Post Tech competency ( You will be assessed as a Pre-Tech before being passed out as a Post Tech ) Post 12 weeks: PAYE 31.65 per hour (33 days accrued leave) / Umbrella 43.21 per hour An additional retainer of 1.00 per hour on all hours worked will be payable. This is subject to tooling returned in satisfactory condition and you have completed the project. This role is inside of IR35 regulations and therefore PAYE or Umbrella Company payment options apply. Benefits PPE provided by Rullion Tooling provided by the Client On-site Messroom with kitchen facilities Coverall cleaning service available Changing facilities with lockers and Showers Qualifications Recognised qualification such as HNC in Electrical of Electronic Engineering Skills required: Practical experience and a sound knowledge of mechanical, electrical and electronic engineering aspects of modern EMU (Electrical Multiple Units) Technical experience and expertise in mechanical and electrical engineering IT Skills - competent user of a PC's including office packages Experience Rolling Stock (Experience on locomotives or other rail vehicles) preferred Requirements You must live within a reasonable travelling distance to our client's facility in Manchester City Centre You must have the right to work in the UK and be able to provide proof of technical qualification Responsibilities Provide technical support to the Overhaul team in the provision of fault-finding expertise and assistance with train repair and train maintenance and test (Where assessed) Partake in gathering required data downloads on critical performance systems. Undertake static testing and dynamic test runs post Overhaul Positioning of fault data into shared drive facility. Carry out fault finding and investigate faults. Component exchange Carry out Testing & Re-Commissioning activities on vehicles and trains in accordance with pre-written test and commissioning procedures. Functionally test train borne systems with minimal supervision using a variety of techniques and methods, including the use of computer-based diagnostics systems. Assist with the validation of documentation issued in support of maintenance and repair activities, special checks, modifications and experiments. Carry out all duties in accordance with the Traincare Centre quality and safety procedures. General depot duties e.g.: Line of Routes Alista, SAP and SES input (Any future business IT systems) Crane driving and lifting equipment where training has been provided & competent. Appointed persons Mentoring others as and when required Understand and abide by safety notices, rules & regulations and follow safe working practices, H&SAWA and COSHH Work in conjunction with our clients lifesaving rules Comply with and enforce our clients Health and Safety Policy Due to working in a safety critical environment, you will be subject to Drugs and Alcohol Testing and will follow strict Health & Safety controls and guidelines. Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants.
Jan 10, 2026
Contractor
Job Title : Rolling Stock Overhaul Technician Overview: You will be based in Manchester, joining a team of over 80 professionals working on a major rolling stock overhaul project for the Class 390 Avanti High Speed Trains. This is an excellent opportunity to be part of a world-leading organisation responsible for maintaining and ensuring the reliability of this iconic, globally recognised fleet. Rullion has a strong long-standing partnership with our client and we place great importance on contractor welfare. Your well being is our priority, with an experienced on-site account manager available to support you throughout the project. This role not only offers an enjoyable working environment, but also the chance to develop valuable skills to progress further in your career. Purpose of Role: You will be working as part of the overhaul team to service, maintain, repair and overhaul rolling stock and equipment, including the latest generation in train technology to laid down Vehicle Maintenance Instructions Ensuring all Overhaul activities are carried out in a safe, efficient and cost-effective manner, whilst constantly seeking to improve quality. Location: Manchester Train Care Centre, Longsight, M12 4HR Start Date: Start of Project = staggered starts each week from 05/01/2026 up to 23/02/2026 Envisaged End Date: End of June 2027 Shift Pattern: Days and Nights on a 2 week shift rotation ( This will take effect once project is in full operation ) Hours: 40 hours on ramp up - 48 hours per week once project is in full operation Start and Finish times: ( Subject to change at client's request ) Days : 07:00 hours to 18:00 hours / 07:00 hours to 15:00 hours Nights : 19:00 hours to 06:00 hours / 20:00 hours to 07:00 hours Overhaul Technician - Pre Tech competency Pre 12 weeks: PAYE 27.41 per hour (28 days accrued leave) / Umbrella 35.47 per hour Post 12 weeks: PAYE 29.53 per hour (33 days accrued leave) / Umbrella 40.32 per hour Overhaul Technician - Post Tech competency ( You will be assessed as a Pre-Tech before being passed out as a Post Tech ) Post 12 weeks: PAYE 31.65 per hour (33 days accrued leave) / Umbrella 43.21 per hour An additional retainer of 1.00 per hour on all hours worked will be payable. This is subject to tooling returned in satisfactory condition and you have completed the project. This role is inside of IR35 regulations and therefore PAYE or Umbrella Company payment options apply. Benefits PPE provided by Rullion Tooling provided by the Client On-site Messroom with kitchen facilities Coverall cleaning service available Changing facilities with lockers and Showers Qualifications Recognised qualification such as HNC in Electrical of Electronic Engineering Skills required: Practical experience and a sound knowledge of mechanical, electrical and electronic engineering aspects of modern EMU (Electrical Multiple Units) Technical experience and expertise in mechanical and electrical engineering IT Skills - competent user of a PC's including office packages Experience Rolling Stock (Experience on locomotives or other rail vehicles) preferred Requirements You must live within a reasonable travelling distance to our client's facility in Manchester City Centre You must have the right to work in the UK and be able to provide proof of technical qualification Responsibilities Provide technical support to the Overhaul team in the provision of fault-finding expertise and assistance with train repair and train maintenance and test (Where assessed) Partake in gathering required data downloads on critical performance systems. Undertake static testing and dynamic test runs post Overhaul Positioning of fault data into shared drive facility. Carry out fault finding and investigate faults. Component exchange Carry out Testing & Re-Commissioning activities on vehicles and trains in accordance with pre-written test and commissioning procedures. Functionally test train borne systems with minimal supervision using a variety of techniques and methods, including the use of computer-based diagnostics systems. Assist with the validation of documentation issued in support of maintenance and repair activities, special checks, modifications and experiments. Carry out all duties in accordance with the Traincare Centre quality and safety procedures. General depot duties e.g.: Line of Routes Alista, SAP and SES input (Any future business IT systems) Crane driving and lifting equipment where training has been provided & competent. Appointed persons Mentoring others as and when required Understand and abide by safety notices, rules & regulations and follow safe working practices, H&SAWA and COSHH Work in conjunction with our clients lifesaving rules Comply with and enforce our clients Health and Safety Policy Due to working in a safety critical environment, you will be subject to Drugs and Alcohol Testing and will follow strict Health & Safety controls and guidelines. Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants.
Data Centre/ Cable Engineer 12 Month Contract Portsmouth, Hampshire 250 Day PAYE Immediate Start 12 Month Contract, possible extension to 18 months or to go permanent Field-role, 20 locations across Hampshire and surrounding areas Full driving license required, vehicle provided We are seeking a number of Data Centre Engineers to support a large installation project starting in February. The role will be hands-on and delivery-focused, covering pre-installation surveys, design validation, physical infrastructure deployment, structured cabling, fibre and copper connectivity, testing, documentation, and health & safety compliance in-line with industry standards and best practice. Responsibilities Pre-Installation Site Surveys The DC Engineer will be responsible for conducting detailed site surveys to validate design assumptions and capture accurate build information, including: Confirm Locations Identify and confirm room and rack locations for all equipment. Validate access routes and working areas. Measure Cable Routes Measure copper and fibre cable lengths from each device to DCN, CIN, and BCH racks. Measure power cable lengths from devices to PDUs. Check Device Interconnects Identify and measure direct links between devices (copper, fibre, DAC, hydra). Record Survey Outputs Produce a list of required cable lengths by type. Confirm final rack positions and room mappings. Provide clear survey documentation to support design and installation. Installation & Build Activities The DC Engineer will perform all physical installation activities on-site, including: Hardware Installation Rack and stack all new network and infrastructure devices. Cabling Between Racks Install structured cabling to BCH racks and UHD shelves/cassettes. Fibre Patching Patch fibre connections to CIN, Transmission platforms, ODFs, and BCH racks as required. Copper Connections Connect copper links to DCN racks and customer handoff/demarcation points. Patch Panel Installation Install ODF panels and hydra cassettes within WWT buildings. Testing & Validation Inspect and clean fibre. Complete power meter and light source testing. Record and evidence pass results. Labelling Label all cabling and hardware in accordance with WWT standards using the Brady BMP61 workflow. Build Documentation Produce as-built documentation including: Photographs Rack layouts Test results Labels & Diagrams Health & Safety Compliance Complete site inductions, RAMS, permits, and adhere to PPE requirements. Maintain controlled workspaces and good housekeeping. Issue Management Log any non-conformances. Remediate issues, re-test, and provide evidence of closure. Design Support The DC Engineer will support the design phase by validating survey data and producing accurate layout documentation, including: Survey Review Review and validate all survey information prior to design commencement. Rack & Space Planning Calculate rack space requirements, equipment footprint, and clearance needs. Equipment Validation Confirm device dimensions, power draw, and suitability for available rack space. Layout Documentation Produce detailed rack layouts showing device positions. Connectivity Definition Document cabling routes, fibre paths, and power connections. Design Drawings Produce final design drawings showing equipment placement and connectivity. Qualifications Proven cabling experience and/or working in data centre environments. Strong knowledge of structured cabling standards (copper & fibre). Experience with rack & stack, patching, ODFs, and hydra cassettes. Comfortable producing as-built documentation and design drawings. Strong understanding of data centre H&S procedures and compliance. Ability to work accurately in live environments.
Jan 09, 2026
Contractor
Data Centre/ Cable Engineer 12 Month Contract Portsmouth, Hampshire 250 Day PAYE Immediate Start 12 Month Contract, possible extension to 18 months or to go permanent Field-role, 20 locations across Hampshire and surrounding areas Full driving license required, vehicle provided We are seeking a number of Data Centre Engineers to support a large installation project starting in February. The role will be hands-on and delivery-focused, covering pre-installation surveys, design validation, physical infrastructure deployment, structured cabling, fibre and copper connectivity, testing, documentation, and health & safety compliance in-line with industry standards and best practice. Responsibilities Pre-Installation Site Surveys The DC Engineer will be responsible for conducting detailed site surveys to validate design assumptions and capture accurate build information, including: Confirm Locations Identify and confirm room and rack locations for all equipment. Validate access routes and working areas. Measure Cable Routes Measure copper and fibre cable lengths from each device to DCN, CIN, and BCH racks. Measure power cable lengths from devices to PDUs. Check Device Interconnects Identify and measure direct links between devices (copper, fibre, DAC, hydra). Record Survey Outputs Produce a list of required cable lengths by type. Confirm final rack positions and room mappings. Provide clear survey documentation to support design and installation. Installation & Build Activities The DC Engineer will perform all physical installation activities on-site, including: Hardware Installation Rack and stack all new network and infrastructure devices. Cabling Between Racks Install structured cabling to BCH racks and UHD shelves/cassettes. Fibre Patching Patch fibre connections to CIN, Transmission platforms, ODFs, and BCH racks as required. Copper Connections Connect copper links to DCN racks and customer handoff/demarcation points. Patch Panel Installation Install ODF panels and hydra cassettes within WWT buildings. Testing & Validation Inspect and clean fibre. Complete power meter and light source testing. Record and evidence pass results. Labelling Label all cabling and hardware in accordance with WWT standards using the Brady BMP61 workflow. Build Documentation Produce as-built documentation including: Photographs Rack layouts Test results Labels & Diagrams Health & Safety Compliance Complete site inductions, RAMS, permits, and adhere to PPE requirements. Maintain controlled workspaces and good housekeeping. Issue Management Log any non-conformances. Remediate issues, re-test, and provide evidence of closure. Design Support The DC Engineer will support the design phase by validating survey data and producing accurate layout documentation, including: Survey Review Review and validate all survey information prior to design commencement. Rack & Space Planning Calculate rack space requirements, equipment footprint, and clearance needs. Equipment Validation Confirm device dimensions, power draw, and suitability for available rack space. Layout Documentation Produce detailed rack layouts showing device positions. Connectivity Definition Document cabling routes, fibre paths, and power connections. Design Drawings Produce final design drawings showing equipment placement and connectivity. Qualifications Proven cabling experience and/or working in data centre environments. Strong knowledge of structured cabling standards (copper & fibre). Experience with rack & stack, patching, ODFs, and hydra cassettes. Comfortable producing as-built documentation and design drawings. Strong understanding of data centre H&S procedures and compliance. Ability to work accurately in live environments.
MSAT Scientist Location: Edinburgh BioQuarter, Little France Who are we? We are RoslinCT, a world-leading cell and gene therapy contract development and manufacturing organisation creating cutting-edge therapies that change people's lives. Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilising ground-breaking science. Find out more about what we do here! Why join us? The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career. A generous salary package - we reward our people at the level they deserve. 31 days of annual leave, plus 4 public holidays which increases with tenure. A competitive company pension scheme to help you save for the future. Group Life Cover - you are automatically covered for three times your basic salary to give you and your family peace of mind. Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us. Flexible benefits such as retail discounts and access to the Cycle2Work scheme. Your new role An exciting opportunity for a MSAT Scientist to join our team. You will be responsible for providing technical support to cell and gene therapy manufacturing processes including: Introduction of new process changes Identifying process improvements and their implementation Implementation of required process documentations to support manufacturing. Support with process monitoring and review process performance Identification, technical/quality assessment and introduction of new materials to manufacturing bill of materials. Providing support for on-floor process trouble shooting, escalation and resolution Quality investigations/out of specification investigations. Provisions of on the floor technical mentoring and guidance to Manufacturing personnel within the cleanroom Manufacturing suite. You will work directly with an MSAT Principal Scientist and collaborate with both internal teams and clients to deliver assigned technical projects/tasks ensuring project timelines are met according to internal and/or customer expectations. You will be an integral part of cross functional project teams including Process Development, Manufacturing, QC, QA, Supply Chain and Project Management to support on-going manufacturing. Write process change controls, validation protocols, risk assessments, batch records and other relevant documentation for both ongoing and new manufacturing processes. Develop new technical protocols, reports and any associated technical documentation to support process transfer and ongoing manufacturing projects. Provide specialist training to manufacturing staff supporting the introduction of new manufacturing processes, changes, and improvements. Support (as SME) technical investigations and out of specifications generating, reviewing, and approving technical reports to support timely close-out of QMS. Support critical process troubleshooting, manage any process escalation being on-call and on-site when required during out of hours and weekends for critical stages of manufacturing. About you Experience within GMP manufacturing and/or process technology transfer roles preferably in the Cell and Gene therapy industry. Hands on cGMP experience with cell culture (2D or 3D system) and other manufacturing process activities. Experience working to EU, MHRA and FDA regulations. Experience in writing technical documents such as process change controls, validation protocols, batch records and standard operating procedures. Excellent attention to detail, proven problem solver, self motivated and positive with a desire to develop technically in your area of expertise. Can do attitude with a determination to succeed and provide solution to complex problems. Contributes to identifying and completing continuous improvement activities to reduce costs, increase yield and productivity for the area. Good organisational and planning skills with the ability to plan whilst delivering results to deadline. Excellent oral and written communication skills; able to explain technical or complex concepts in a clear format to both technical and non technical audiences. Proven ability to learn and share knowledge with the rest of the manufacturing team and enable them to successfully perform new manufacturing processes. Qualifications A degree in a Life Science discipline or relevant equivalent experience.
Jan 09, 2026
Full time
MSAT Scientist Location: Edinburgh BioQuarter, Little France Who are we? We are RoslinCT, a world-leading cell and gene therapy contract development and manufacturing organisation creating cutting-edge therapies that change people's lives. Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilising ground-breaking science. Find out more about what we do here! Why join us? The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career. A generous salary package - we reward our people at the level they deserve. 31 days of annual leave, plus 4 public holidays which increases with tenure. A competitive company pension scheme to help you save for the future. Group Life Cover - you are automatically covered for three times your basic salary to give you and your family peace of mind. Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us. Flexible benefits such as retail discounts and access to the Cycle2Work scheme. Your new role An exciting opportunity for a MSAT Scientist to join our team. You will be responsible for providing technical support to cell and gene therapy manufacturing processes including: Introduction of new process changes Identifying process improvements and their implementation Implementation of required process documentations to support manufacturing. Support with process monitoring and review process performance Identification, technical/quality assessment and introduction of new materials to manufacturing bill of materials. Providing support for on-floor process trouble shooting, escalation and resolution Quality investigations/out of specification investigations. Provisions of on the floor technical mentoring and guidance to Manufacturing personnel within the cleanroom Manufacturing suite. You will work directly with an MSAT Principal Scientist and collaborate with both internal teams and clients to deliver assigned technical projects/tasks ensuring project timelines are met according to internal and/or customer expectations. You will be an integral part of cross functional project teams including Process Development, Manufacturing, QC, QA, Supply Chain and Project Management to support on-going manufacturing. Write process change controls, validation protocols, risk assessments, batch records and other relevant documentation for both ongoing and new manufacturing processes. Develop new technical protocols, reports and any associated technical documentation to support process transfer and ongoing manufacturing projects. Provide specialist training to manufacturing staff supporting the introduction of new manufacturing processes, changes, and improvements. Support (as SME) technical investigations and out of specifications generating, reviewing, and approving technical reports to support timely close-out of QMS. Support critical process troubleshooting, manage any process escalation being on-call and on-site when required during out of hours and weekends for critical stages of manufacturing. About you Experience within GMP manufacturing and/or process technology transfer roles preferably in the Cell and Gene therapy industry. Hands on cGMP experience with cell culture (2D or 3D system) and other manufacturing process activities. Experience working to EU, MHRA and FDA regulations. Experience in writing technical documents such as process change controls, validation protocols, batch records and standard operating procedures. Excellent attention to detail, proven problem solver, self motivated and positive with a desire to develop technically in your area of expertise. Can do attitude with a determination to succeed and provide solution to complex problems. Contributes to identifying and completing continuous improvement activities to reduce costs, increase yield and productivity for the area. Good organisational and planning skills with the ability to plan whilst delivering results to deadline. Excellent oral and written communication skills; able to explain technical or complex concepts in a clear format to both technical and non technical audiences. Proven ability to learn and share knowledge with the rest of the manufacturing team and enable them to successfully perform new manufacturing processes. Qualifications A degree in a Life Science discipline or relevant equivalent experience.
Job title: Rolling Stock Overhaul Electrical Technician Job Type: Temporary Contract IR35 Status: Inside IR35 Start date: Immediate Duration: 12 month contract Potential for extension Pay rate: Competitive Location: Longsight, Manchester, M12 4HR Hours of work: Full Time - 40.00 per week (48 hours per week once fully operational) Shift pattern: Days & Nights Mon-Fri on a 2-week rotating shift (once fully operational) The Opportunity Rullion are proud to be recruiting an Overhaul Electrical Technician to support a major rolling stock overhaul programme based in Manchester. You'll be joining a well-established, highly skilled team of over 80 rail professionals, working on the overhaul of Class 390 high-speed trains - one of the most iconic and technically advanced fleets operating in the UK today. This is an excellent long-term contract opportunity to work at a state-of-the-art Train Care Centre, contributing to the reliability, safety and performance of a globally recognised high-speed fleet. The Role As an Overhaul Electrical Technician, you will play a key role in the service, maintenance, repair and overhaul of modern rolling stock, working in line with detailed Vehicle Maintenance Instructions (VMIs). Safety, quality and continuous improvement will be at the heart of everything you do. Key Responsibilities Provide technical support and fault-finding expertise to the overhaul team Carry out electrical fault diagnosis, investigation and rectification Undertake component exchange, testing and re-commissioning activities Perform static testing and support dynamic test runs post-overhaul Download, analyse and record data from critical performance systems Functionally test train-borne systems using computer-based diagnostic tools Accurately record fault data and upload to shared systems Support validation of maintenance, repair and modification documentation Use depot systems including Alista, SAP and SES (or future IT systems) Carry out general depot duties, including Line of Route tasks Operate cranes and lifting equipment (where trained and competent) Mentor colleagues and support team development when required Always work in compliance with safety rules, H&S legislation, COSHH and lifesaving rules What We're Looking For Qualifications HNC in Electrical or Electronic Engineering (or higher), or NVQ Level 3 in Electrical Engineering Skills & Knowledge Strong practical knowledge of electrical, electronic and mechanical systems Experience working on modern EMUs or similar complex assets Confident using IT systems and computer-based diagnostics Experience Rolling Stock experience preferred Applicants from Aerospace, Heavy Transport, Electric Vehicles or Ex-Forces Engineering backgrounds are also encouraged to apply Additional Requirements Must live within a reasonable commuting distance of Manchester Right to work in the UK Ability to provide proof of technical qualifications Willingness to work days and nights on a rotating shift pattern What's On Offer Long-term contract with strong potential for extension PPE provided by Rullion Full tooling provided on site On-site mess room with kitchen facilities Coverall cleaning service Changing facilities, lockers and showers Safety This is a safety-critical environment. Successful candidates will be required to undergo Drugs & Alcohol testing and work in strict accordance with Health & Safety controls and procedures at all times. If you're an experienced Electrical Technician looking to work on a flagship high-speed rail project in Manchester, this is a standout opportunity to advance your rail career with the support of a specialist recruitment partner. Please note that applicants must have the right to work in the UK. We cannot provide VISA sponsorship. Interested in this position? please click "apply now" We try to respond to all applicants, but sometimes this is not possible due to high volumes of applications; if you have not heard from us within 14 days, regrettably it means you have been unsuccessful on this occasion. This vacancy is being advertised by Rullion Ltd acting as an employment business Since 1978, Rullion has been securing exceptional candidates for a range of clients; from large well-known brands, to SMEs and start-ups. As a family-owned business, Rullion's approach is credible and honest, focused on building long-lasting relationships with both clients and candidates. Rullion is a forward-thinking recruitment company that specialises in providing a wide range of talent consultancy services to a diverse client base; from small start-ups to large household names. We celebrate and support diversity and are committed to ensuring equal opportunities for both employees and applicants. Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants.
Jan 07, 2026
Contractor
Job title: Rolling Stock Overhaul Electrical Technician Job Type: Temporary Contract IR35 Status: Inside IR35 Start date: Immediate Duration: 12 month contract Potential for extension Pay rate: Competitive Location: Longsight, Manchester, M12 4HR Hours of work: Full Time - 40.00 per week (48 hours per week once fully operational) Shift pattern: Days & Nights Mon-Fri on a 2-week rotating shift (once fully operational) The Opportunity Rullion are proud to be recruiting an Overhaul Electrical Technician to support a major rolling stock overhaul programme based in Manchester. You'll be joining a well-established, highly skilled team of over 80 rail professionals, working on the overhaul of Class 390 high-speed trains - one of the most iconic and technically advanced fleets operating in the UK today. This is an excellent long-term contract opportunity to work at a state-of-the-art Train Care Centre, contributing to the reliability, safety and performance of a globally recognised high-speed fleet. The Role As an Overhaul Electrical Technician, you will play a key role in the service, maintenance, repair and overhaul of modern rolling stock, working in line with detailed Vehicle Maintenance Instructions (VMIs). Safety, quality and continuous improvement will be at the heart of everything you do. Key Responsibilities Provide technical support and fault-finding expertise to the overhaul team Carry out electrical fault diagnosis, investigation and rectification Undertake component exchange, testing and re-commissioning activities Perform static testing and support dynamic test runs post-overhaul Download, analyse and record data from critical performance systems Functionally test train-borne systems using computer-based diagnostic tools Accurately record fault data and upload to shared systems Support validation of maintenance, repair and modification documentation Use depot systems including Alista, SAP and SES (or future IT systems) Carry out general depot duties, including Line of Route tasks Operate cranes and lifting equipment (where trained and competent) Mentor colleagues and support team development when required Always work in compliance with safety rules, H&S legislation, COSHH and lifesaving rules What We're Looking For Qualifications HNC in Electrical or Electronic Engineering (or higher), or NVQ Level 3 in Electrical Engineering Skills & Knowledge Strong practical knowledge of electrical, electronic and mechanical systems Experience working on modern EMUs or similar complex assets Confident using IT systems and computer-based diagnostics Experience Rolling Stock experience preferred Applicants from Aerospace, Heavy Transport, Electric Vehicles or Ex-Forces Engineering backgrounds are also encouraged to apply Additional Requirements Must live within a reasonable commuting distance of Manchester Right to work in the UK Ability to provide proof of technical qualifications Willingness to work days and nights on a rotating shift pattern What's On Offer Long-term contract with strong potential for extension PPE provided by Rullion Full tooling provided on site On-site mess room with kitchen facilities Coverall cleaning service Changing facilities, lockers and showers Safety This is a safety-critical environment. Successful candidates will be required to undergo Drugs & Alcohol testing and work in strict accordance with Health & Safety controls and procedures at all times. If you're an experienced Electrical Technician looking to work on a flagship high-speed rail project in Manchester, this is a standout opportunity to advance your rail career with the support of a specialist recruitment partner. Please note that applicants must have the right to work in the UK. We cannot provide VISA sponsorship. Interested in this position? please click "apply now" We try to respond to all applicants, but sometimes this is not possible due to high volumes of applications; if you have not heard from us within 14 days, regrettably it means you have been unsuccessful on this occasion. This vacancy is being advertised by Rullion Ltd acting as an employment business Since 1978, Rullion has been securing exceptional candidates for a range of clients; from large well-known brands, to SMEs and start-ups. As a family-owned business, Rullion's approach is credible and honest, focused on building long-lasting relationships with both clients and candidates. Rullion is a forward-thinking recruitment company that specialises in providing a wide range of talent consultancy services to a diverse client base; from small start-ups to large household names. We celebrate and support diversity and are committed to ensuring equal opportunities for both employees and applicants. Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants.
Microbiology Manager page is loaded Microbiology Managerlocations: UK - Stevenagetime type: Full timeposted on: Posted Todayjob requisition id: JR100071 Work with us Our team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working environment which actively promotes creativity, leadership and teamwork - together we are ONE Autolus. Job Description: Job Title: Manager, QC - MicrobiologyReports to: Senior Manager, QC MicrobiologyDepartment: Quality ControlHours: Full Time (Sunday - Wednesday, 0800AM - 545PM).Location: Stevenage About Autolus Autolus is a biopharmaceutical company, advancing innovative therapies at both clinical and commercial stages of development, focused on next-generation, programmed T cell therapies for the treatment of cancer. Using a broad suite of proprietary and modular T cell programming technologies, the company is engineering precisely targeted, controlled, and highly active T cell therapies designed to better recognize cancer cells, break down their defence mechanisms, and eliminate these cells. Autolus has a pipeline of product candidates in development for the treatment of haematological malignancies, solid tumours, and autoimmune diseases.Autolus is a biopharmaceutical company, advancing innovative therapies at both clinical and commercial stages of development, focused on next-generation, programmed T cell therapies for the treatment of cancer. Using a broad suite of proprietary and modular T cell programming technologies, the company is engineering precisely targeted, controlled, and highly active T cell therapies designed to better recognize cancer cells, break down their defence mechanisms, and eliminate these cells. Autolus has a pipeline of product candidates in development for the treatment of haematological malignancies, solid tumours, and autoimmune diseases. Why Autolus Our team is passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy to deliver life-changing treatments to patients. Whilst working at Autolus you will enjoy a flexible, diverse, and dynamic working environment which actively promotes creativity, leadership and teamwork. In addition to this Autolus is proud to offer a competitive salary, performance related bonus as well as private medical insurance, life assurance, pension and access to an employee share scheme. Our Promise Autolus is developing complex breakthrough therapies for a globally diverse market and equally recognises that diversity amongst our people is critical to our mission. As we draw on our differences, what we've experienced, and how we work, we celebrate diversity and are committed to creating an inclusive environment for all employees. Role Summary Quality Control Microbiology manages and executes routine safety testing using validated analytical methods and following prescribed testing plans. Function is responsible for execution and management of environmental monitoring programs in Autolus manufacturing facilities. In addition, microbiology function also manages the process of operator aseptic qualification and aseptic process simulation. QC Microbiology plays an important role in Autolus' Sterility Assurance and Contamination Control Strategy programme.QC Manager (Microbiology) leads a team of Microbiologists covering 7 days operation. Job holder is responsible for efficient provision of QC Microbiology services to production and other internal and external customers by overseeing testing schedules, schedule adherence to comply with internal and external deadlines, and establishing effective communication between all stakeholders. The QC Manager monitors, maintains and drives continuous improvement in compliance and an analytical programme within the team and across the department, and drives streamlining of processes with a focus of removing waste. The QC Microbiology Manager will also interact with multiple functions within the business to guarantee smooth and concise information exchange. Key Responsibilities Ensuring adherence to Health and Safety (HSE) policies and procedures within the team Managing a team of Pharmaceutical Microbiologists (performance assessments, improvement, and development plans) Establishing SMART objectives for team members in alignment with overall QC and business objectives, and continuous progress monitoring Managing QC schedule (creation, adherence) to ensure timely delivery of results to production and allow timely batch disposition/certifications Managing workload and capacity for the team and assigning adequate priorities (capacity plan) Maintaining the QC laboratory in inspection ready state Overviewing, assigning and ensuring adequate training level within the team Collation and presentation of team metrics and data Driving and contributing to ongoing optimisation of our existing processes and analytical methods incl. automatization Managing the batch certification process (e.g., data review, approval, quality events) Developing and implementing continuous improvement projects using LEAN Overseeing Deviations (QE's), Change requests, Laboratory Investigations, SOPs, together with leading systematic problem solving Looking after the wellbeing of the team Coordination of shift activities with Production counterparts (e.g. Environmental Monitoring in Production Cleanroom facility) Cooperation with other QC Managers to ensure testing and compliance continuity Execution of self-inspections within QC and implementation of CAPA Cross functional teamworking e.g. with Production, Validation and Engineering to ensure GMP status of analytical instruments and QC facilities Working closely with QA to efficiently manage all aspects of quality and compliance related to Quality Control On call for EMS system in QC laboratory Any other duties as required following consultation with the post holder Experience of Pharmaceutical Regulatory Agency GMP inspections (e.g., MHRA, FDA, EMA) is preferred. Demonstrated skills and competencies E - Essential P - Preferred Experience Min 3 years' experience as a Microbiology Manager in GxP regulated environment, preferably from within QC function within ATMPs, Biologicals or Biopharmaceuticals managing testing teams. Min 5 years' experience in Microbiology Laboratory facility Qualifications BSc/MSc degree in life sciences (P) or significant relevant industry experience Skills/Specialist knowledge Open to working shifts (E) Previously experience preferred working in a cleanroom, and/or aseptic environment (P) Conflict resolution skills (E) Experience and demonstrated knowledge of aseptic techniques and practices Experience in troubleshooting and relevant tools (5xWhy, Root Cause Analysis) Extensive knowledge of LEAN, GMP & Microbiology Experience within EM, ID and BI analysis including Mycoplasma and Endotoxin testing (P) Familiarity with Annex 1 and Contamination Control Strategies for (E) Familiarity with analytical procedure lifecycle (validation, tech transfer, verification) (P) Familiarity with regulations governing Stability testing and shelf-life management (P) Familiarity with analytical equipment qualification lifecycle (P) Experience with QMS quality events and Out of Specification (OOS) in Environmental Monitoring (application, conduct, timely closure) (E) Demonstrated experience of representing a function at high level cross-functional meetings with minimal support required (E) Highly Proficient in MS Word, Excel, Power Point, DOE and any other relevant applications (E) Demonstrated experience in mentorship, supervision, and management of experienced members of team (E) Great ability to identify and
Jan 01, 2026
Full time
Microbiology Manager page is loaded Microbiology Managerlocations: UK - Stevenagetime type: Full timeposted on: Posted Todayjob requisition id: JR100071 Work with us Our team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working environment which actively promotes creativity, leadership and teamwork - together we are ONE Autolus. Job Description: Job Title: Manager, QC - MicrobiologyReports to: Senior Manager, QC MicrobiologyDepartment: Quality ControlHours: Full Time (Sunday - Wednesday, 0800AM - 545PM).Location: Stevenage About Autolus Autolus is a biopharmaceutical company, advancing innovative therapies at both clinical and commercial stages of development, focused on next-generation, programmed T cell therapies for the treatment of cancer. Using a broad suite of proprietary and modular T cell programming technologies, the company is engineering precisely targeted, controlled, and highly active T cell therapies designed to better recognize cancer cells, break down their defence mechanisms, and eliminate these cells. Autolus has a pipeline of product candidates in development for the treatment of haematological malignancies, solid tumours, and autoimmune diseases.Autolus is a biopharmaceutical company, advancing innovative therapies at both clinical and commercial stages of development, focused on next-generation, programmed T cell therapies for the treatment of cancer. Using a broad suite of proprietary and modular T cell programming technologies, the company is engineering precisely targeted, controlled, and highly active T cell therapies designed to better recognize cancer cells, break down their defence mechanisms, and eliminate these cells. Autolus has a pipeline of product candidates in development for the treatment of haematological malignancies, solid tumours, and autoimmune diseases. Why Autolus Our team is passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy to deliver life-changing treatments to patients. Whilst working at Autolus you will enjoy a flexible, diverse, and dynamic working environment which actively promotes creativity, leadership and teamwork. In addition to this Autolus is proud to offer a competitive salary, performance related bonus as well as private medical insurance, life assurance, pension and access to an employee share scheme. Our Promise Autolus is developing complex breakthrough therapies for a globally diverse market and equally recognises that diversity amongst our people is critical to our mission. As we draw on our differences, what we've experienced, and how we work, we celebrate diversity and are committed to creating an inclusive environment for all employees. Role Summary Quality Control Microbiology manages and executes routine safety testing using validated analytical methods and following prescribed testing plans. Function is responsible for execution and management of environmental monitoring programs in Autolus manufacturing facilities. In addition, microbiology function also manages the process of operator aseptic qualification and aseptic process simulation. QC Microbiology plays an important role in Autolus' Sterility Assurance and Contamination Control Strategy programme.QC Manager (Microbiology) leads a team of Microbiologists covering 7 days operation. Job holder is responsible for efficient provision of QC Microbiology services to production and other internal and external customers by overseeing testing schedules, schedule adherence to comply with internal and external deadlines, and establishing effective communication between all stakeholders. The QC Manager monitors, maintains and drives continuous improvement in compliance and an analytical programme within the team and across the department, and drives streamlining of processes with a focus of removing waste. The QC Microbiology Manager will also interact with multiple functions within the business to guarantee smooth and concise information exchange. Key Responsibilities Ensuring adherence to Health and Safety (HSE) policies and procedures within the team Managing a team of Pharmaceutical Microbiologists (performance assessments, improvement, and development plans) Establishing SMART objectives for team members in alignment with overall QC and business objectives, and continuous progress monitoring Managing QC schedule (creation, adherence) to ensure timely delivery of results to production and allow timely batch disposition/certifications Managing workload and capacity for the team and assigning adequate priorities (capacity plan) Maintaining the QC laboratory in inspection ready state Overviewing, assigning and ensuring adequate training level within the team Collation and presentation of team metrics and data Driving and contributing to ongoing optimisation of our existing processes and analytical methods incl. automatization Managing the batch certification process (e.g., data review, approval, quality events) Developing and implementing continuous improvement projects using LEAN Overseeing Deviations (QE's), Change requests, Laboratory Investigations, SOPs, together with leading systematic problem solving Looking after the wellbeing of the team Coordination of shift activities with Production counterparts (e.g. Environmental Monitoring in Production Cleanroom facility) Cooperation with other QC Managers to ensure testing and compliance continuity Execution of self-inspections within QC and implementation of CAPA Cross functional teamworking e.g. with Production, Validation and Engineering to ensure GMP status of analytical instruments and QC facilities Working closely with QA to efficiently manage all aspects of quality and compliance related to Quality Control On call for EMS system in QC laboratory Any other duties as required following consultation with the post holder Experience of Pharmaceutical Regulatory Agency GMP inspections (e.g., MHRA, FDA, EMA) is preferred. Demonstrated skills and competencies E - Essential P - Preferred Experience Min 3 years' experience as a Microbiology Manager in GxP regulated environment, preferably from within QC function within ATMPs, Biologicals or Biopharmaceuticals managing testing teams. Min 5 years' experience in Microbiology Laboratory facility Qualifications BSc/MSc degree in life sciences (P) or significant relevant industry experience Skills/Specialist knowledge Open to working shifts (E) Previously experience preferred working in a cleanroom, and/or aseptic environment (P) Conflict resolution skills (E) Experience and demonstrated knowledge of aseptic techniques and practices Experience in troubleshooting and relevant tools (5xWhy, Root Cause Analysis) Extensive knowledge of LEAN, GMP & Microbiology Experience within EM, ID and BI analysis including Mycoplasma and Endotoxin testing (P) Familiarity with Annex 1 and Contamination Control Strategies for (E) Familiarity with analytical procedure lifecycle (validation, tech transfer, verification) (P) Familiarity with regulations governing Stability testing and shelf-life management (P) Familiarity with analytical equipment qualification lifecycle (P) Experience with QMS quality events and Out of Specification (OOS) in Environmental Monitoring (application, conduct, timely closure) (E) Demonstrated experience of representing a function at high level cross-functional meetings with minimal support required (E) Highly Proficient in MS Word, Excel, Power Point, DOE and any other relevant applications (E) Demonstrated experience in mentorship, supervision, and management of experienced members of team (E) Great ability to identify and
