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FM Project Manager - Oxford Your new company We’re seeking a proven Project Manager to lead site delivery at a scientific laboratory in Oxford. You’ll take full ownership of the programme, quality, cost, and safety—driving the plan from tender through to handover. This is a hands-on leadership role: managing site teams and subcontractors, liaising closely with the client and designers, and ensuring the project is delivered on time, on budget, and to exacting standards. Your new role KEY RESPONSIBILITIES • Lead and manage all site staff to achieve programme, quality, and safety objectives., • Drive project planning and sequencing; monitor and report against milestones., • Manage tenders and procurement from inception to completion., • Control and optimise labour, plant, and material resources., • Ensure full compliance with company procedures and site-specific protocols., • Champion Health, Safety, Environmental and Quality (HSEQ) requirements at all times., • Maintain high standards of workmanship and quality assurance on site., • Track progress, risks, and change; maintain robust project controls and records., • Deliver the programme and budget; implement corrective actions where required., • Manage and monitor subcontractor performance; chair regular subcontractor meetings., • Liaise proactively with the client, designers, and the wider project management team., • Chair and attend progress meetings; compile and present clear progress reports., • Produce and distribute accurate meeting minutes and action trackers., • Maintain contractual records and support commercial control, including cost management., • Identify and implement improvements and innovations to enhance delivery., • Positively represent and promote the company on site and with stakeholders., • Proven experience delivering complex construction projects as a Project Manager (live, technical, or regulated environments advantageous)., • Strong leadership of site teams and subcontractors with a collaborative, results-driven approach., • Excellent planning, programming, and progress control skills., • Solid commercial awareness with experience controlling costs, change, and risk., • Clear communicator | Confident chairing meetings and producing professional reports and minutes., • Thorough understanding of HSEQ management and compliance., • Strong client-facing skills with the ability to build trust and manage expectations., • SMSTS, • Black CSCS, • Relevant construction/engineering degree or equivalent experience., • First Aid at Work., • Competitive day rate dependent on experience., • Ongoing Training & Development., • Discounted Private Health Care Scheme. 4759084

Managing Quantity Surveyor, Oxford Location: Oxford Industry: Water / Wastewater Scope of Work: A key role within the commercial team delivering major wastewater infrastructure works on a landmark project in Oxford. Are you an experienced Quantity Surveying professional with experience in delivering across the commercial facets of projects? Have you ambitions to work on large-scale infrastructure projects? Turner Lovell is recruiting a Managing Quantity Surveyor to join a leading, highly innovative, multi-national engineering services company in the UK. This is a brilliant opportunity for the right individual to join a well established, highly regarded business that is experiencing growth through their success in the market. You will be working on site in Oxford, with commercial responsibility across multiple phases of this multi-year project. With the support or the wider team, your responsibilities will include: • Play an active part in culture of the team by encouraging and developing the commercial awareness of junior staff; motivation, performance oversight and delegation; ensuring the site team adheres to group procedures and governance., • Preparation of internal commercial reporting; valuations / application for payment with full supporting documentation in accordance with the contract; Cost Reports to the Client with contractually compliant supporting documentation; and management of subcontract and material procurement schedules., • Administration of subcontractor / supplier accounts from the preparation of detailed requisitions, monitoring and authorisation of subcontract payments through to agreement of final accounts., • Undertake the contract administration, including change management and maintain associated registers; identifying commercial risks, opportunities, value engineering and change; challenging & managing in cost control / cost mitigation., • Assisting with preparation of the Cost to Complete and Risk analysis Register for the projects(s); ensuring appropriate Client Management is initiated and maintained; and maintain / assist in the production of the margin improvement plan on the project. The ideal profile is someone with: • Degree Qualification in Quantity Surveying, • Chartered or on route to achieving chartership, • Strong communication skills including ability to present, to negotiate and to lead a team, • Computer literate with strong skills in Microsoft office applications, • Full driving license If you are considering what your next role could look like within Quantity Surveying, and have a passion for playing a part in delivering landmark projects, please apply and get in touch with Mark Canning via the link provided for more information.

ROLE: Commercial Estimating Engineer/Manager LOCATION: Oxfordshire SALARY: £45,000 - £55,000 per annum JOB TYPE: Full-time Overview: We are seeking a Commercial Estimating Engineer to join a precision engineering and manufacturing business based in Oxford. This role is pivotal in evaluating customer enquiries, producing accurate and timely manufacturing cost estimates, and managing contracts from initial enquiry through to completion. The successful candidate will combine strong technical knowledge with commercial awareness, customer engagement, and a right-first-time mindset. Key Responsibilities: • Evaluate customer enquiries for machined components and assemblies, interpreting engineering drawings and digital data to define manufacturing requirements., • Produce accurate and competitive cost estimates and quotations within agreed timeframes, clearly documenting assumptions and methodologies., • Develop optimum manufacturing methods, capturing all relevant technical and commercial information to support quoting decisions., • Project manage new business opportunities, generating project plans and required documentation., • Prepare clear and concise quotations, submitting for internal review prior to customer issue., • Conduct quick-load activities for new orders, ensuring all material, specification, and process information is captured prior to release., • Carry out detailed contract reviews, adopting a critical approach to ensure clarity, compliance, and right-first-time delivery., • Negotiate raw material pricing and place purchase orders as required, liaising with suppliers and sourcing new vendors for outsourced processes., • Provide technical support relating to methods, tooling, and manufacturing strategy throughout the contract lifecycle., • Monitor contract profitability and review performance with production and supply chain teams, identifying opportunities for cost reduction and process improvement., • Actively contribute to continuous improvement initiatives focused on quality, delivery, and cost., • Maintain regular communication with customers, ensuring they are kept informed throughout the contract., • Ensure strict adherence to company safety, quality, and conduct procedures., • Maintain a clean, organised, and professional working environment., • Work collaboratively within the team, sharing best practice and supporting colleagues as required. Skills & Experience: • Apprentice-trained engineer or equivalent qualification in a mechanical or engineering discipline., • Strong background in mechanical engineering with the ability to interpret complex engineering drawings and technical information., • Previous experience within a subcontract machining environment is highly advantageous., • Commercial awareness with experience estimating, quoting, or managing engineering contracts., • Strong communication skills, both written and verbal, with the ability to engage effectively at all levels., • Good level of IT literacy, including familiarity with ERP or estimating systems., • Proactive, flexible, and positive “can-do” attitude with a strong work ethic., • Knowledge of Continuous Improvement and Lean Manufacturing principles is beneficial., • Experience in an account management or customer-facing engineering role is advantageous.

Are you immediately available and looking for a Project Management role with an innovative Biotech Company? Do you have prior experience in Project Management , operations or a similar role in life sciences? We are currently seeking a Project Manager to join a Biotech company in Oxford. You will partner with and support the COO to deliver key operational projects. This is an ideal role if you have prior experience in Project Management/ Operations within a Biotech Start up or the life science sector, and you are immediately available for a new challenge. Role Overview • £26-£31ph DOE., • Initially Temporary (3-6 months), Full Time (37.5 per week, Mon-Fri,). Start Date ASAP, • Work directly with the COO to provide project and operational support – planning , coordinating and executing key projects., • Work collaboratively with internal project teams and external suppliers to ensure effective communication and maintain project timelines., • Support the preparation of relevant documentation including reports, and executive communications. Including summary and preparation/presentation of material for the Senior Leadership Team. Requirements • BSc Degree or equivalent, ideally in a relevant scientific subject., • 1-3 years of experience in a similar Project Management or Operational role, ideally within a small biotech (or similar) organisation., • Excellent organisational, time management and analytical skills., • Excellent communication skills , both written and verbal. Prior experience of presenting to senior leadership/ c-suite is highly beneficial., • Must be Available to begin immediately in Oxford (OX4) In return This is an excellent opportunity to gain additional experience working with an innovative , high growth start up Biotech company. You will work closely with Senior Leadership during an exciting time of development and work on projects with a direct impact on achieving the company’s mission of improving patient’s lives. For more information or to apply, please contact Louis Williams. Due to the volume of applications received on a daily basis, we find it incredibly difficult to respond to each and every one. Should you not hear back from us within two weeks, please assume your application was unsuccessful on this occasion. Network Scientific is an award-winning science recruitment agency specialising in the provision of temporary, permanent and contract recruitment services to the scientific and related technical industries. We’re an ethical and knowledgeable consultancy passionate about our candidate care. If you feel this role is not right for you but are interested in other opportunities in the Scientific sector, please take a look at our company website. Please note that all applicants for this role should be able to prove that they are legally entitled to work in the UK. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency

! Location: Need to be located close to Oxfordshire Start date: ASAP Shift Pattern: 2-2-3 (Panama Schedule) | 7:00am – 7:00pm Work Arrangement: Site-based (no remote work) Type of position: Freelance. Minimum 6 month contract with the view to extend Job Description Planet Pharma are working with a biotechnology company known for pioneering work in messenger RNA (mRNA) science. Its focus is on developing medicines that use mRNA to instruct the body’s cells to produce proteins that can prevent or treat disease. The organisation operates across infectious diseases, oncology, rare conditions, and immune disorders, and it became widely recognised for creating one of the first mRNA‑based vaccines during the global pandemic. Beyond vaccines, it continues to expand its therapeutic pipeline, invest heavily in research platforms, and partner with global health and scientific institutions to advance next‑generation treatments. Description: Joining this organisation offers the chance to contribute to a pioneering environment advancing the use of mRNA technology in modern medicine. With a broad and growing pipeline across multiple therapeutic areas, you will collaborate with talented colleagues and global partners, playing a direct role in improving health outcomes worldwide. As part of a long‑term commitment to strengthening onshore mRNA vaccine manufacturing in the UK, a state‑of‑the‑art research, development, and production facility is being established in Oxfordshire. This initiative will support respiratory vaccine manufacturing, create highly skilled roles, and promote collaboration with academic institutions, the NHS, and government partners across the country. We are seeking motivated and detail‑oriented professionals to support 24/7 manufacturing operations, with a focus on end‑to‑end warehouse and logistics activities. This Fixed‑Term Contract position is essential to maintaining compliant, efficient material flow for real‑time mRNA production. You will gain hands‑on experience with SAP, Quality Management Systems (QMS), and digital workflows—building strong foundations for future automation and AI‑enabled operational environments. Key Responsibilities • Receive and process inbound deliveries, ensuring documentation is accurate and resolving any discrepancies., • Upload delivery and quality records into the organisation’s QMS to maintain full GMP compliance., • Pick, verify, and stage materials required for mRNA manufacturing in line with production schedules., • Apply internal standards for labelling, handling, storage, and inventory control within a GxP‑regulated setting., • Perform daily SAP transactions related to inventory movements and stock accuracy., • Support outbound logistics, including shipment preparation and documentation., • Conduct cycle counts and reconcile physical inventory with SAP data., • Identify, segregate, and manage expired or non‑conforming materials., • Work closely with logistics and operations teams to ensure seamless support across the facility., • Complete all required training to meet compliance, quality, and safety expectations. Requirements: • Good experience in warehouse operations ideally in life science or food industry, • Experience working in a GMP / GDP environment., • Knowledge of Quality Management Systems (QMS)., • Ability to lift and move products safely., • Flexibility to meet operational demands., • Strong attention to detail with a collaborative, customer-focused approach. If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help! About Planet Pharma Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

Technical Buyer – Metal Powders & Critical Materials Location: Oxford (up to 1 day from home/week) Salary: £50,000 to £60,000 per annum + Excellent Benefits Type: Full-Time, Permanent Overview A forward-thinking, technology-led manufacturer in the advanced materials sector is seeking a Technical Buyer to oversee the procurement of metal powders, critical production materials, and globally sourced components. This role plays a vital part in ensuring a secure, cost-effective and compliant supply chain, supporting both day-to-day operations and long-term production strategy. Ideal for someone with procurement experience in a manufacturing setting, particularly involving metals, powders or advanced components, the position requires strong commercial acumen, supplier management capability and the ability to coordinate international logistics within a fast-paced environment. Key Responsibilities Sourcing and Supplier Management • Source and onboard suppliers for powders and production-critical inputs, • Negotiate commercial terms and maintain supplier pricing and performance data, • Translate production schedules and MRP signals into timely purchase orders, • Maintain accurate ERP data on lead times, costs and inventory parameters, • Monitor material, freight and inventory costs and identify efficiencies, • Maintain supplier risk registers and ensure data accuracy across systems, • Oversee inbound shipments and international logistics, including customs compliance, • Supervise goods-in processes, ensuring accurate receipt, traceability and stock control, • Lead and support the Goods-In and Inventory function, • Develop SOPs across procurement, inventory and logistics operations, • Drive continuous improvement and cross-functional alignment with Engineering, Quality and Finance Candidate Profile Essential Experience and Skills • Procurement or supply chain experience within a manufacturing environment, • Background in powders, metals or technical materials (preferred), • ERP or MRP proficiency and strong data management discipline, • Understanding of incoterms, customs and international logistics, • Experience with traceability, batch control and quality systems, • Proactive with a strong ownership mindset, • Analytical and commercially aware, • Collaborative and process-focused, • Detail-oriented with a strong safety ethos This is a high-impact role within a cutting-edge manufacturing environment. If you're looking to apply your procurement expertise in a technical and fast-moving setting, we encourage you to apply.

Deliver high quality novel characterisation capability in the field of nuclear materials through own endeavour and creative input. Build and provide management to a small team of material scientists and engineers providing research direction and allocating them to projects as required. Lead in

Your responsibilities will include maintaining the Master Production Schedule and Material Requirements Planning, managing resource capacity, routing work orders, and collaborating closely with Manufacturing, Supply Chain and Project Management.

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 Validation Specialist to join our Validation Equipment team. In this role, you willhave theopportunity to participate in high value projects, working alongside cross-functional teams to deliver company goals, contribute to the delivery of major customer projects and the ensuring of regulatory compliance for GMP systems, playinga key part in advancing our mission and making a real difference. Your responsibilities in this role would be: Preparation and execution of validation deliverables for GMP systems. Providing SME support from Validation for project activities related to GMP systems. Active participation in cross-functional meetings and discussions to provide validation support to both internal and customer SMEs. Ownership of quality records (Deviations, Change Controls and CAPAs) on behalf of the Validation Department. Supporting Validation activities duringTechnology Transfer of new systems. Contributing to the maintenance of overall department KPIs relating to validation of equipment, facilities, utilities, processes and computerised systems. Profile description: We are looking for: A degree (or equivalent) in a Science / Engineering or related discipline. Experience in laboratory systems qualification, including automated systems. Strong background on validation of systems with CSV component. Proven experience withinthe generation/execution of equipment validation lifecycle documents (URS, DQ, IQ, OQ, PQ, RQ & RTM) A working knowledge of the current standards, GMP regulations and industry guidelines as they relate to qualification/validation of GMP systems. Experience of working within a GMP Quality Management System. Highly organised individual with aproven ability for problem-solving, thoroughness and good teamwork. Demonstratable effective oral, written & interpersonal skills. The ability to adapt to changes in priorities and meeting timelines. Highly motivated individual with ability to identify and implement continuous improvement activities We offer: 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

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 Sample Management Coordinator to join our Quality ControlTeam . In this role, you will receive, store, issue, pack, ship, organise and dispose of samples in a controlled manner , playing a key part in advancing our mission and making a real difference. *Please note this is not considered an undergraduate opportunity at OXB. Please see Scientist II, Production Biotechnologist QC Officer, or QC Microbiologist or other similar II level opportunities on our career site for these types of roles. Your responsibilities in this role would be: Receiving samples from manufacturing sites, checkingcondition, ensuring samples are logged inand stored appropriately Organising and preparing outgoing shipments of samples to external testing organisations / clients Navigating LIMS processes for sample management activities Ensuring any discrepancies are noted and dealt within a timely manner Ensuring a good standard of record keeping and documentation Authoring and reviewing of Standard Operating Procedures (SOPs) and other documentation Ownership and troubleshooting of processes to ensure procedural efficiencies Responsible for liaising and leading meetings with other teams / departments We are looking for: Educated to a minimum of?GCSE or equivalent qualification level orable todemonstraterequired skillsgained withinanotherworkplace Experience using LIMS (not essential) A genuine interest and drive to work in science Good interpersonal and communication skills (written and verbal) Highly organised and motivated with excellent attention to detail Knowledge and experience of MS Office, Word, Excel & Outlook 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 than30years of experience in viral vectors; the driving force behindthe majority ofgene therapies. OXB collaborates with some of the worlds most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturingexpertisein 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 regulatoryexpertise. 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

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 aTechnical Writer to join our Process Development team. The purpose of this role is to collaborate with Scientists in the effective reporting of experimental data from work carried out within the PD department, playing a key part in advancing our mission and making a real difference. Your responsibilities in this role would be: Preparation and authoring of clear and concise documentation including protocols and scientific reports to support Upstream and Downstream process development activities. Standardisation of PD documentation to ensure technical presentations, protocols and reports meet OXB and client needs and are delivered within project timelines. Support digitisation programmes aimed to reduce report turnaround times and ensure consistent, compliant reports. Maintain a high standard of record keeping so that information is clearly captured, disseminated, and reported. Disseminate critical findings which may have a business impact to other departments within the company. Function as a department Technical Writing Subject Matter Expert, this includes the delivery of technical writing training to the department. Ensure all scientific or proprietary data is submitted or recorded in appropriate official documentation. Maintain a high ethical standard and a commitment to producing high quality work. We are Looking For: A graduate or postgraduate degree (or equivalent level qualification) in a relevant science Previous operational experience within a Process development or GMP Manufacturing environment. A sound understanding of basic biopharmaceutical process development activities. Industry experience in authoring biopharma process development reports would be advantageous. A high standard or of written and verbal communication skills in English. The ability to collaborate cross departmentally to achieve PD departmental goals. Highly organised and the ability to manage multiple tasks & projects. Excellent organisational and time management skills 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 programsthat 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? Profile description: ,, 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 Maintenance Engineer with the ability to work across both Mechanical & Electrical maintenance disciplines to join the Engineering team . In this role, you will determine and execute routine preventative maintenance activities and procedures and assess and implement major fault repairs, playing a key part in advancing our mission and making a real difference. Your responsibilities in this role would be: Accountable for completion of assigned routine preventative maintenance activities Identification and mitigation of equipment faults. Responding to breakdowns of equipment, assessment, diagnosis, repair of faults or escalation Co-ordinating of OXBs external engineering resource in relationship to specialist repairs and maintenance of assets Completing regulatory routine monitoring Evaluating asset performance against determined criteria Completing quality documentation for critical failures Escalating events impacting engineering assets. Identification and management of critical engineering stock inventory. Maintain a safety-first approach to assets and engineering procedures. Profile description: We are looking for: A minimum of 5 GCSEs (or equivalent) including Maths and English An apprenticeship to NVQ 3 Level 3, City & Guilds or equivalent in mechanical and/or electrical engineering. Experience within a GxP Pharmaceutical/Biotech industry is preferred or alternatively a similar regulated environment. Good working knowledge of Health and Safety within an engineering environment is needed. We offer: 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 TPBN1_UKTJ

Are you ready to lead a team at a state-of-the-art automotive facility where precision, quality, and innovation drive every vehicle we help create? We are seeking a Production Team Leader to join our dedicated quality management team onsite at a state-of-the-art automotive production facility, where advanced engineering and precision manufacturing combine with British heritage to deliver iconic, high-quality premium cars. Benefits include: £13.50 per hour Shift allowance of 25% after 22:00pm Weekend overtime available in peak times starting from 25%+ 28 days holiday - Inclusive of Bank Holidays Free on-site parking Employer pension contribution Excellent training and development opportunities Reporting to the Shift Manager, the Production Team Leader, will be responsible for leading and coaching a team of between 5 - 10 quality inspectors, which can increase during peak times. You will work alongside management to successfully organise and lead the hour-to-hour function of designated projects within associated G&P areas. Working hours are as follows: AM Shift - 05:45am - 16:15pm PM Shift - 16:15pm - 02:00am Monday - Friday /Overtime available on weekends Responsibilities include but are not limited to: Leading and coaching a team of quality professionals Reviewing handover from previous shift and assigning tasks to the Quality Inspectors and Storemen in accordance. Ensuring all quality inspectors have the relevant tooling, material flow, PPE and understanding to work to the required Test Plan / WES. Controlling all NOK parts found during the project, ensuring the packaging and stacking of parts are correct. Working alongside the area supervisor to identify and promptly resolve issues, with minimal or no effect to production. Leading from the front by carrying out inspection duties alongside the team as and when required. The ideal production team leader will have the following experience: Proven leadership skills ideally gained within a similar environment such as production, manufacturing, logistics, engineering or quality inspection. Computer literate, including Microsoft Word, Excel and Outlook. Excellent communication skills Ability to resolve issues promptly, within a professional manner. Organised, resilient, with the ability to think outside the box. Nice to have experience, but not essential: Previous experience using SAP Knowledge of writing work instructions This is a permanent position with progression opportunities available - Candidates must have the independent right to work in the UK; sponsorship is not available. If this role sounds like it could be of interest, then please apply today for a confidential chat. G&P is a world-leading quality management services provider, supporting manufacturers in the automotive, defence, aerospace and industrial sectors, and their associated supply chains, to transform quality and efficiency levels. With over 30 years of experience, we provide tailored solutions through senior management support and expert personnel from our dedicated talent division. Through our award-winning engineering, technical, inspection and talent services, we help businesses minimise risk, maximise performance and achieve operational excellence. Operating from strategic hubs in six countries, we continue to grow across new sectors, always focused on eliminating disruptions and supporting our clients drive to zero defects. G&P is an equal opportunities employer and do not discriminate on the grounds of gender, sexual orientation, marital or civil partner status, pregnancy or maternity, gender reassignment, race, colour, nationality, ethnic or national origin, religion or belief, disability or age. TPBN1_UKTJ

Our prestigious client is seeking an Employment Tax Manager for their busy team based in Reading, but they would consider their Oxford office too. In this role you will be responsible for managing a portfolio of clients, providing expert advice on employment tax matters, and supporting clients with compliance, risk management, and planning opportunities. You will oversee client relationships, lead projects, manage junior staff, and contribute to the development of the firm's employment tax service line. Key Responsibilities as Employment Tax Manager Advisory & Compliance Advise clients on all aspects of employment tax, including PAYE, NIC, benefits-in-kind, expenses, termination payments, off-payroll working (IR35), and employment status. Manage employer compliance processes, including PAYE Settlement Agreements (PSAs), P11Ds, and HMRC disclosures. Support clients with HMRC enquiries, audits, and settlements. Provide strategic advice on workforce planning, reward structures, expatriate tax issues, and employee share schemes (where applicable). Client Management & Business Development Act as the main point of contact for a portfolio of clients, ensuring excellent service delivery. Identify new advisory opportunities and support business development initiatives. Assist in preparing and presenting proposals, thought leadership, and marketing material. Practice Contribution Support the senior leadership team in growing the employment tax practice. Ensure compliance with risk management and quality control procedures. Stay up to date with legislative changes, case law, and HMRC guidance to maintain technical excellence. The person: ATT/CTA or equivalent qualification essential. Strong knowledge of UK employment tax legislation and HMRC practices. Previous experience in an employment tax role within a professional services firm or HMRC. Proven ability to manage client relationships and deliver high-quality advice. Experience in managing HMRC enquiries and negotiations. Strong analytical, problem-solving, and report-writing skills. Excellent communication skills, with the ability to explain complex tax issues clearly. Experience of supervising or mentoring junior team members. Proactive, with the ability to manage multiple projects and deadlines. Strong team player with leadership potential. Enthusiastic about contributing to the growth of the practice. 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 Manufacturing Equipment & Systems Specialist to join our Manufacturing team . In this role youll ensure that all equipment and computerised systems are compliant, safe, and maintained to support efficient batch delivery, playing a key part in advancing our mission and making a real difference. If you enjoy problem-solving, working with high-tech equipment, and being the go-to person for technical queries, this is a great opportunity to make a real impact. Please note this role is an onsite opportunity which doesnt require shift work. Your responsibilities in this role would be: Managing equipment documentation (audit trails, asset folders, user access). Controlling access to manufacturing systems and supporting trained personnel. Supporting equipment moves, installations, and validation lifecycle activities (URS, DQ, RQ, VRR, CST). Maintaining and updating asset materials such as logbooks and SOPs. Acting as a technical contact for Quality, Validation, Engineering, audits, and client queries. Working with equipment vendors to resolve technical issues and support purchasing/spares. Supporting equipment-related NPI activities, pre-batch readiness, and shutdown periods. Participating in HAZOP reviews and acting as SME for equipment-related QMS records. We are looking for: Ability to travel across all Oxfordshire sites. STEM degree desirable or relevant industry experience. Knowledge of GMP and cleanroom environments. Experience with manufacturing equipment such as bioreactors or chromatography systems. Understanding of Quality Management Systems (CAPA, CC, DEV). Ability to follow SOPs and complete cleanroom gowning qualification. 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. TPBN1_UKTJ

Material Bank is the fastest and most powerful way for design professionals to search, sample, and specify materials. As Director, Account Management - Europe, you will play a critical role in strengthening and scaling Material Bank’s brand partner ecosystem across the region. Material Bank is the

You’ll manage and maintain up-to-date Insight specifications for all raw materials, ensure supplier approval is rock solid, and risk assess each material to meet food safety, customer and legal requirements. If you’re ready to make your mark at the very start of the food production process – w

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Inventory Control,Procurement,SAP,Supply Chain Experience,SAP Supply Chain Management,Production Planning,Supplier Management,ERP Systems,Materials Management,Logistics,Manufacturing,MRP. If your next Supply Chain Manager job needs to be with a company that has the security and maturity of a large e

Inventory Control,Procurement,SAP,Supply Chain Experience,SAP Supply Chain Management,Production Planning,Supplier Management,ERP Systems,Materials Management,Logistics,Manufacturing,MRP. Budget management and cost control experience. Oversee inventory control cost management and revenue tracking.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Inventory Control,Procurement,SAP,Supply Chain Experience,SAP Supply Chain Management,Production Planning,Supplier Management,ERP Systems,Materials Management,Logistics,Manufacturing,MRP. Execution of Scripted activities to deliver optimum schedules (for Exceptions Inventory Management & Data Ma

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Inventory Control,Procurement,SAP,Supply Chain Experience,SAP Supply Chain Management,Production Planning,Supplier Management,ERP Systems,Materials Management,Logistics,Manufacturing,MRP. Engineering management experience ideally obtained from working in a highly-regulated manufacturing environment.

Storage of material in accordance with material control and product preservation procedures. Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety. Goods In - Visual inspection and acceptance of incoming material and packaging to ensure consignments

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

You will also be provided access to a free mobile phone app with a wealth of wellness material as well as free counselling sessions provided by qualified independent professionals. Ugo Foods Group has internally developed and promoted over 50% of its internal management team from entry-level positio

Utilise inventory management systems to maintain accurate records and uphold product quality during handling. Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

To receive and book in raw materials. Locate raw materials in both Gate 1 and Gate 2 Warehouse as required. Process and load Baxter goods and Raw Materials for dispatch.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Work from drawings bills of materials to estimate materials and labor pricing. Kanban,Inventory Control,Purchasing,Maximo,SAP,Supply Chain Experience,Production Planning,SAP ERP,ERP Systems,Materials Management,Manufacturing,MRP. Advise management of the status of work in progress by coordinating wi

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

The successful candidate will follow standard work for goods in material handling and perform all activities in accordance with safety and quality rules. Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Utilise inventory management systems to maintain accurate records and uphold product quality during handling. Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Abinitio,Electronic Security,Internship,Learning Management System,Airport,Environment Health And Safety.

Accountable for initial documentation generation to support change management and business realization. BA in supply chain management technical field (biotechnology biology chemistry pharmacy engineering or related disciplines) or data science; a Masters or MBA preferred.