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ROLE REQUIREMENTSTo be successful in your application to this exciting role as the Applications Scientist we are looking to identify the following on your profile and past history:A Degree or higher level in Chemistry (e. Key Words: Applications Scientist / Membrane Development / Chemical Research /

ROLE OVERVIEWWe are currently looking for a Quality Assurance Specialist to join a leading organisation within the life sciences sector. This is an exciting opportunity for a dedicated professional to contribute to maintaining the highest standards of quality and compliance across manufacturing processes.This role offers the chance to work within a dynamic team, supporting continuous improvement initiatives and ensuring products meet stringent regulatory requirements. Our client values proactive individuals who are passionate about quality and can make a meaningful impact in a fast-paced environment.KEY DUTIES AND RESPONSIBILITIESYour duties as the Quality Assurance Specialist will be varied however the key duties and responsibilities are as follows: • To ensure that all products and processes adhere to internal quality standards and external regulatory requirements. • Conduct and support audits, reviews, and inspections to maintain compliance and identify areas for improvement. • Assist in the development, implementation, and maintenance of quality management systems. • Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. • As the Quality Assurance Specialist, you will play a pivotal role in ensuring continuous compliance and fostering a culture of quality excellence.ROLE REQUIREMENTSTo be successful in your application to this exciting role as the Quality Assurance Specialist we are looking to identify the following on your profile and past history: • A Degree or higher level in a relevant field (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management for QA roles). • Proven experience within quality assurance, ideally in a manufacturing environment, demonstrating knowledge of regulatory standards such as GMP or ISO. • Strong attention to detail, problem-solving skills, and the ability to work effectively within a team.WHAT’S IN IT FOR YOU?Joining our client offers the opportunity to develop your career in a leading organisation renowned for quality standards. You will be supported in your professional growth while working on impactful projects in a collaborative environment. Competitive benefits and a commitment to innovation are also key aspects of this role.Key Words: Quality Assurance / GMP / ISO / Regulatory Compliance / Continuous Improvement / Manufacturing / Life Sciences / Teamwork / Career Development"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career".

\n Job purpose\n \n Reporting to the President & Chief Executive Officer (CEO) and the Global Head of R&D, the Head of Research & Development (R&D) will play a lead role in delivering business critical R&D programmes. The Head of R&D is a member of the Molecular Imaging Senior Leadership Team and will have management responsibility for the following functions: Biometrics; Chemistry, Manufacturing & Control (CMC); Clinical Operations; Editorial (Medical Writing); Imaging; Non-Clinical; R&D Programme Management \n \n Main Responsibilities, Activities, Duties and Tasks\n \n \n \n • Biometrics (to include biostatistics, statistical programming, and data management), ensuring operational delivery and the provision of strategic advice concerning statistical methods and data management activities.\n \n • Chemistry, Manufacturing & Control (CMC) ensuring the robust manufacturing and supply of materials used in the manufacture of investigational and finished commercial radiopharmaceutical products.\n \n • Clinical operations, ensuring operational delivery and the provision of strategic advice concerning the design, feasibility and execution of all clinical studies.\n \n • Editorial (medical writing), ensuring the development and implementation of strategic publication plans and the dissemination of scientific and clinical data (e.g., via manuscripts and conference presentations).\n \n • Imaging, providing medical physics support, including radiation physics, medical imaging physics and imaging analytics expertise.\n \n • Non-clinical, to include evaluations of non-clinical toxicology, safety and efficacy.\n \n • R&D programme management, including: Delivery of the programme strategy (in accordance with the Long-Range Plan and in close collaboration with colleagues in Clinical Development, Commercial, Finance, Innovation & Strategy, Legal (incl. Intellectual Property), Medical Affairs, Pharmacovigilance & Quality and Regulatory Affairs). Operational oversight and project delivery, in compliance with applicable laws, industry codes and regulations Budget management (including Long-Range Planning, Annual Budget and Rolling Forecast 2 & 3 and related resource allocation & planning), Portfolio review, Risk management, Regular reporting to the Executive Committee and Board of Directors including progress in achieving strategic objectives; advising of any significant variance from the approved strategic plans and budget; and any significant programme issues.\n \n • Research and Development Collaborating with the New Asset Evaluation Team, specifically on the identification and technical assessment of new licensing, lifecycle and geographic expansion opportunities.\n \n • Collaborations with academia, pharma and imaging equipment providers.\n \n • All matters of significant organisational structure within R&D, including development of the capabilities of the internal workforce and the recruitment, promotion, retention, succession planning & dismissal of employees, in conjunction with Human Resources.\n \n • Establish or implement departmental policies, goals, objectives, or procedures in conjunction with the Leadership Team and Global R&D at Bracco.\n \n • Other duties as determined by business needs.\n \n \n \n Education/Qualifications\n \n \n \n • Educated to at least degree level, preferably with a PhD in science or life science (or equivalent research experience).\n \n • Professional Experience, Knowledge, & Technical Skills Significant experience in clinical drug development and particularly the development of medical imaging agents and radiopharmaceuticals is key, as is significant experience of staff & performance management. A strong scientific background in a relevant area in a relevant scientific discipline an advantage and awareness of relevant guidelines and regulations governing drug development activities, particularly imaging drugs, a pre-requisite. Knowledge of Regulatory Authority (i.e., EMA, FDA) and Good Clinical Practice (GCP) guidelines.\n \n • Proven leadership, organisational, facilitation, negotiation, collaboration, empowerment, and interpersonal skills with the ability to work effectively with others at all levels of the organisation.\n \n • Experience with cross-functional and highly matrixed organizations.\n \n • Ability to coach, mentor, develop and educate direct reports.\n \n • Excellent written and verbal communication.\n \n \n \n Soft Skills – Company Values & Behaviours\n \n \n \n • Excellent interpersonal skills, including communication verbally and in writing.\n \n • Ability to influence and build relationships in a global organisation.\n \n • Excellent organisational skills, including multitasking, efficiency, punctuality, and project management.\n \n • Excellent collaboration skills including experience in a cross-functional and highly matrixed organisation.\n \n \n \n Contract type: Permanent \n \n At Bracco, we believe in the values of diversity and inclusion. We respect and celebrate the diversity of our people and their experiences, ensuring a fair opportunity for all. \n \n We are #Bracco #JoinUs Improve people’s lives by shaping the future of prevention and precision imaging. This is our purpose. Our work impacts millions of people all over the world. Not least the more than 4,000 Bracco colleagues who work to improve lives every single day. That is quite a responsibility and something we proudly embrace. We are the Bracco Group! \n #J-18808-Ljbffr

Do you want to contribute to a safer market while gaining an authentic international experience as a consultant? \n \n Obelis is currently looking for a Regulatory Affairs & Food Safety Consultant! \n \n Your role will be: \n As a Regulatory Affairs & Food Safety Consultant, you will play a key role in supporting the Regulatory Affairs Department (RA) by providing senior regulatory expertise, overseeing complex projects, and contributing to the team's performance, operational efficiency, and achievement of departmental KPIs. \n \n Your responsibilities will include: \n 1.Lead complex regulatory projects and provide expert regulatory guidance with a focus on food safety compliance. \n 1. Review and validate complex documentation and authority interactions. \n 1. Drive technical excellence and departmental expertise. \n 1. Act as a trusted advisor for strategic clients. \n 1. Coach colleagues and support managers in coordination activities. \n 1. Participate in Obelis events (in and outside the UK) \n 1. Support safe market access and work in an international consulting environment. The successful candidate will support clients on regulatory matters across the UK, EU, and US, with a primary focus on food safety, supporting appropriate regulatory oversight and accountability for food safety compliance activities. \n 1. Deliver professional, responsive, and high-quality service to external and internal clients. \n 1. Act as, or work towards becoming, the designated Food Supplement PRRC, ensuring appropriate oversight of food safety regulatory compliance activities in line with internal procedures and applicable requirements. \n 1. Provide regulatory support covering UK, EU, and US product requirements, with particular emphasis on food safety and related product categories. \n 1. Perform borderline assessments to support appropriate product classification, including food safety versus medicine, medical device, cosmetic, or other regulated product categories. \n 1. Assess product composition, ingredients, claims (e.g. nutrition and health claims, including permitted claims, on-hold botanical claims, disease-risk reduction claims, and the avoidance of prohibited medicinal claims), labelling, and supporting documentation for regulatory compliance. \n \n Requirements \n\n • Applicants must hold a valid UK work permit.\n, • Bachelor's/Master's degree in Food Science, Nutrition, Pharmacy, Chemistry, Toxicology, Biology or a related scientific discipline.\n, • 3+ years of relevant experience in the food safety consultancy sector.\n, • Fluency in English (written and oral). Knowledge of additional languages is a plus.\n, • Strong knowledge of regulatory applications and documentation review\n, • Solid understanding of regulatory environments and their impact on clients.\n, • Analytical mindset with the ability to translate issues into practical improvements.\n, • Ability to work cross-functionally across teams and stakeholders.\n\n \n Training & Development \n At Obelis, we believe in continuous learning and professional growth. In this role, you will further develop your expertise in: \n\n • Regulatory strategy and expert advisory\n, • Project and stakeholder management\n, • Client advisory and relationship management\n, • Regulatory risk assessment and decision-making\n\n \n Benefits & Conditions \n\n • Location: Oxford\n, • Full-time position\n, • Hybrid work setting\n\n \n Company Profile \n Obelis s.a is a quality-driven, service-oriented company, with over 30 years of experience in EU Regulations. Providing consultancies on medical devices, cosmetics, and other consumer goods, we believe in making manufacturers better through compliance and making safe products available on the market.

Our client a well established and well known business within the Nuclear setor are currently looking to hire a Waste Engineer/Package Manager to be part of a busy project based in Culham, Oxforshire on a contractual basis. This is an exciting opportunity for an experienced Waste Engineer to play a key role in the Decommissioning & Repurposing Programme. Working within a highly regulated nuclear environment, you will lead waste engineering activities across major decommissioning projects, ensuring safe, compliant and cost-effective waste management solutions.Job Title: Waste Engineer/Package ManagerDuration: 12 MonthsLocation: Culham, OxfordshireWorking Week: 4 Days Per Week OnsiteRates: Competitive Hourly Rates - Inside IR35Key Responsibilities:Develop and deliver waste management strategies for decommissioning projects.Lead waste characterisation activities, including DQOs, WSAPs and sampling campaigns.Identify suitable treatment, recycling and disposal routes for radioactive and hazardous waste.Coordinate contractors, laboratories and specialist suppliers.Work closely with project teams, health physics, environmental specialists and regulators.Manage technical risks and provide guidance to junior engineers and graduates.Skills/Experience Required:Degree-qualified in Engineering, Environmental Science, Physics, Chemistry or a related discipline.Significant experience in waste management, decommissioning or another highly regulated industry.Strong understanding of radioactive waste characterisation, classification and disposal.Knowledge of UK nuclear and environmental regulations (IRR17, EPR, CDM).Excellent stakeholder engagement, problem-solving and technical report-writing skills.Chartered status or equivalent experience is advantageous.A Full Job Specification can be provided.TPBN1_UKTJ

Shift operations TechnicianC£58,000 + BonusArdleyMC Technical Recruitment is currently looking to recruit working on a 24-hour shift rotation, operating an Energy Recovery Facility safely and efficiently from the control room and in the field.This role will involve safely operating the Energy Recovery Facility from both the control room and on-site, monitoring plant performance, responding to faults, carrying out plant isolations, and ensuring safe, efficient and environmentally compliant operations.Working 40 hours per week, on a 5-week shift pattern, include nights.As a Shift Operations Technician, you will be responsible for:Operating the DCS and responding to alarms.Monitoring and optimising plant performance.Diagnosing and rectifying process/equipment faults.Carrying out plant isolations and safe systems of work.Monitoring boiler chemistry and environmental compliance.Completing accurate shift logs and handovers.Other duties as requiredTo be considered for this role you should have:Mechanical, electrical or process plant experienceUnderstanding of plant isolations and safe systems of work.Strong fault-finding and problem-solving skills.IOSH or NEBOSH (preferred).Ability to attain Authorised Person status (desirable).This is an exciting opportunity to join a leading business with huge growth potential.The offer:The package on offer for this role includesA salary up to £58,000 depending on experienceAnnual BonusPension schemeHolidaysOther benefitsTo apply:If you are interested in this role please apply via the link below or contact Machaela at MC Technical Recruitment on 01489533030 / for a confidential chat.TPBN1_UKTJ

ROLE REQUIREMENTSTo be successful in your application to this exciting role as the Head of R&D we are looking to identify the following on your profile and past history:A Degree or higher level in Chemistry, Materials Science or a closely related discipline. As the Head of R&D, you will support and

ROLE OVERVIEWWe are currently looking for a Research Scientist with expertise in Synthetic Organic Chemistry to join a leading innovator in chemistry materials based in the Oxfordshire area. This is an exciting opportunity for a motivated scientist to contribute to groundbreaking projects with vario

Join Us in Changing LivesAt OXB, our people are at the heart of everything we do. We’re on a mission to enable life-changing therapies to reach patients around the world—and we’re looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.We’re currently recruiting for a VP, Global External Quality to join our Global Quality team. In this role, you will lead the development and execution of the Global External Quality strategy, providing oversight across data integrity, external manufacturing partners, suppliers, and client-facing quality activities, playing a key part in advancing our mission and making a real difference.This role can be located close by one of our global locations in Oxford, UK, or Strasbourg or Lyon in France.Your responsibilities in this role would be to:Develop and lead the global External Quality and Data Integrity strategy, ensuring alignment with corporate objectives, regulatory requirements, customer expectations, and the long-term needs of the external manufacturing and supplier network.Embed a proactive quality culture across external partners by driving accountability, risk identification, compliance, and quality-focused decision making.Lead quality transformation and continuous improvement programmes that enhance compliance, operational excellence, digital quality capabilities, risk management, and overall business performance.Provide strategic leadership and governance as a member of the Global Quality Leadership Team, contributing to enterprise-wide quality strategy, decision making, and cross-functional alignment.Establish and oversee a comprehensive Data Integrity programme, ensuring compliance with ALCOA+ principles, risk management, training, monitoring, investigations, and remediation across internal and external networks.Lead Supplier Quality Management, including supplier qualification, risk assessment, quality agreements, performance monitoring, audits, governance, and supplier development programmes to drive compliance, reliability, and performance.Provide quality oversight for external manufacturing partners, ensuring effective governance, quality reviews, performance management, and risk mitigation.Act as the senior quality representative for clients and customers, leading quality governance, supporting audits and due diligence, resolving quality issues, and building trusted relationships that support commercial and business development objectives.We are looking for:Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline; advanced degree preferred.Extensive experience within the biotechnology and/or pharmaceutical industry, including senior Quality leadership roles in regulated manufacturing environments.Strong knowledge of global regulatory authorities including FDA, GMP, GCP and GLP requirements.Proven expertise in Quality Management Systems (QMS), with a particular focus on GMP compliance and data integrity.Demonstrated experience with regulatory inspections, audits, and quality assurance activities, including supplier quality management.In-depth understanding of risk management, validation and qualification principles, and quality performance metrics.About Us:OXB (LSE: OXB) is a global quality and innovation-led contract development and manufacturing organisation (CDMO) in cell and gene therapy 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, OXB has 30 years of experience in viral vectors; the driving force behind the majority of cell and gene therapies. 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), adenovirus and other viral vector types. OXB’s world-class capabilities range from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise.OXB offers a vast number of technologies for viral vector manufacturing, including a 4th generation lentiviral vector system (the TetraVecta system), a dual-plasmid system for AAV production, suspension and perfusion process using process enhancers and stable producer and packaging cell lines.OXB, a FTSE250 and FTSE4Good constituent, is headquartered in Oxford, UK. It has development and manufacturing facilities across Oxfordshire, UK, Lyon and Strasbourg, France, Bedford MA, and Durham NC, US.Why Join Us?ð Competitive total reward packagesð§ Wellbeing programs that support your mental and physical healthð Career development opportunities to help you grow and thriveð Supportive, inclusive, and collaborative culture𧪠State-of-the-art labs and manufacturing facilitiesð A company that lives its values: Responsible, Responsive, Resilient, RespectWe want you to feel inspired every day. At OXB, we’re future-focused and growing fast. We succeed together—through passion, commitment, and teamwork.#LI-RB1 #LI-HYBRID Ready to Make a Difference?

Chemistry Laboratory Technician (Operator) 24-25k South East ABJ6515 TEMP - 6 months – on site An excellent opportunity for an early-career Chemistry Laboratory Technician / Lab Operator to join a dynamic and supportive team within a modern laboratory environment. This role is ideal for someon

Biology Lead, Plant Science, Discovery Research, R&D Mentorship A Biology Lead opportunity has opened up at an innovative agricultural biotech company operating at the forefront of sustainable crop protection science. This is a rare chance to step into a senior scientific leadership position where your expertise will directly shape the direction of a growing discovery biology function. Could this be the role where your scientific thinking makes a genuine difference to how the next generation of herbicides are developed? The Role The Biology Lead will serve as the senior scientific authority within the discovery function, providing expert guidance across biological platforms, assay development, experimental design and data-driven decision-making. You will work closely with chemistry, project management and technical operations colleagues to ensure that biological insight is fully embedded in candidate progression and portfolio decisions. A key part of this role is being present and visible within the laboratory, not to oversee every experiment, but to troubleshoot, advise on protocols and help scientists think through challenges in real time. Beyond day-to-day scientific guidance, the Biology Lead will champion rigorous experimental standards and reproducible data practices across the function, lead the uptake of new methodologies and tools, and represent the company professionally in external collaborations and partnerships. You will also coach and develop scientists at all levels, raising the quality of scientific thinking across the team rather than managing headcount. The Company This is an opportunity to join an ambitious and growing biotech company based in South East England, focused on discovering novel crop protection solutions. The organisation brings together a multidisciplinary team of scientists working across discovery, chemistry and technical operations to develop sustainable agricultural products. It is a science-first culture that values collaborative working, evidence-based decision-making and the kind of creative rigour that accelerates genuine discovery. The company works with a range of external scientific partners, including academic collaborators, CROs and commercial partners. What experience does the Biology Lead need? PhD-qualified scientist with a strong research background and the ability to apply deep biological expertise to complex discovery challenges. Established scientific leader with experience mentoring and influencing multidisciplinary teams, driving technical excellence without necessarily having extensive line management responsibilities. Commercial R&D experience, ideally working across collaborative research programmes, external partnerships and cross-functional project teams. Hands-on and scientifically curious, with a passion for staying close to the science and supporting experimental problem-solving. Experience in plant science, crop protection or related life sciences is advantageous, but exceptional candidates from biotech or pharmaceutical discovery who are keen to transition into the sector will also be considered. Excellent communicator who can translate complex scientific concepts into clear recommendations and influence stakeholders across technical and leadership teams. So What's Next? If you are a Biology Lead and would like to learn more, please apply below and I will be in touch with you shortly to discuss the role further. Biology Lead Corriculo Ltd acts as an employment agency and an employment business. #CL #indhigh TPBN1_UKTJ

Delivering engaging Chemistry lessons at IGCSE and A-Level. Proven experience teaching Chemistry.

Develop students' conceptual understanding of physical, organic, and inorganic chemistry. Integrate technology, simulations, and digital resources to enhance Chemistry learning. Master's degree in Chemistry or a relevant subject from a recognised university.

Degree or background in Chemistry, Analytical Chemistry, Biochemistry, Industrial/Process Chemistry or similar. Temporary Chemist – Pilot Plant, on-site for 6 months.

Helio Display Materials Limited is seeking a highly motivated synthetic/process development chemist to advance perovskite nanocrystal technology. You will bridge R&D and scale-up, developing robust synthetic methods and understanding chemistry to inform early manufacturing decisions.

As part of our Product Development team, you will be working with senior chemists to support the company pilot line. HNC/HND, Bachelor's degree, or equivalent qualification in Chemistry or a related scientific discipline. Experience working in an industrial or research chemistry laboratory.

HydRegen, an innovative biotechnology company, seeks a Chemist for its Chemistry R&D team in Oxford.You will develop, optimise and scale catalytic hydrogenation processes in a hands-on lab environment, delivering high-quality data to support product development and customer projects.The role require

Astrophoria Foundation Year Teaching Associates for Chemistry, Engineering, Materials Science (CEMS) Course. The Astrophoria Foundation Year Programme seeks to appoint Teaching Associates (TAs) for the Chemistry, Engineering and Materials Science (CEMS) course. To make informal enquiries about the p

The University of Oxford is seeking applications for a Research Associate in Mass Spectrometry. Ideal candidates will have an undergraduate degree in Chemistry and relevant experience in mass spectrometry and analytical chemistry.

Join an innovative chemistry company based in Oxfordshire, specialising in advanced materials technologies as a Research Scientist. To apply for this Research Scientist position, please submit your CV and a cover letter detailing your relevant experience and why you are interested in this role. Rese

The Postdoctoral Research Associate will join the Department of Chemistry at the University of Oxford to work on functional polymer and synthetic host-guest chemistry. Applicants should have a PhD in Chemistry (or near completion), with experience in molecular synthesis, functional polymer synthesis

Advanced Science, Advanced Materials, and other Advanced journals, Angewandte Chemie, Chemistry Europe titles, and Small is expanding and therefore looking for an additional Assistant Editor. Job Responsibilities:· Be responsible for the organization of the peer-review process and editorial

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 VP, Global External Quality to join our Global Quality team. In this role, you will lead the development and execution of the Global External Quality strategy, providing oversight across data integrity, external manufacturing partners, suppliers, and client-facing quality activities, playing a key part in advancing our mission and making a real difference. This role can be located close by one of our global locations in Oxford, UK, or Strasbourg or Lyon in France. Your responsibilities in this role would be to: Develop and lead the global External Quality and Data Integrity strategy, ensuring alignment with corporate objectives, regulatory requirements, customer expectations, and the long-term needs of the external manufacturing and supplier network. Embed a proactive quality culture across external partners by driving accountability, risk identification, compliance, and quality-focused decision making. Lead quality transformation and continuous improvement programmes that enhance compliance, operational excellence, digital quality capabilities, risk management, and overall business performance. Provide strategic leadership and governance as a member of the Global Quality Leadership Team, contributing to enterprise-wide quality strategy, decision making, and cross-functional alignment. Establish and oversee a comprehensive Data Integrity programme, ensuring compliance with ALCOA+ principles, risk management, training, monitoring, investigations, and remediation across internal and external networks. Lead Supplier Quality Management, including supplier qualification, risk assessment, quality agreements, performance monitoring, audits, governance, and supplier development programmes to drive compliance, reliability, and performance. Provide quality oversight for external manufacturing partners, ensuring effective governance, quality reviews, performance management, and risk mitigation. Act as the senior quality representative for clients and customers, leading quality governance, supporting audits and due diligence, resolving quality issues, and building trusted relationships that support commercial and business development objectives. We are looking for: Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline; advanced degree preferred. Extensive experience within the biotechnology and/or pharmaceutical industry, including senior Quality leadership roles in regulated manufacturing environments. Strong knowledge of global regulatory authorities including FDA, GMP, GCP and GLP requirements. Proven expertise in Quality Management Systems (QMS), with a particular focus on GMP compliance and data integrity. Demonstrated experience with regulatory inspections, audits, and quality assurance activities, including supplier quality management. In-depth understanding of risk management, validation and qualification principles, and quality performance metrics. About Us: OXB (LSE: OXB) is a global quality and innovation-led contract development and manufacturing organisation (CDMO) in cell and gene therapy 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, OXB has 30 years of experience in viral vectors; the driving force behind the majority of cell and 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), adenovirus and other viral vector types. OXBs world-class capabilities range from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods and depth of regulatory expertise. OXB offers a vast number of technologies for viral vector manufacturing, including a 4th generation lentiviral vector system (the TetraVecta system), a dual-plasmid system for AAV production, suspension and perfusion process using process enhancers and stable producer and packaging cell lines. OXB, a FTSE250 and FTSE4Good constituent, is headquartered in Oxford, UK. It has development and manufacturing facilities across Oxfordshire, UK, Lyon and Strasbourg, France, Bedford MA, and Durham NC, US. 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. #LI-RB1 #LI-HYBRID Ready to Make a Difference? TPBN1_UKTJ

Medicinal Chemistry Research Scientist, 18-month contract. Vertex are seeking a motivated and enthusiastic organic chemist to join their growing Medicinal Chemistry team as a Research Scientist at their Milton Park R&D site in Oxford. As a member of the medicinal chemistry team, you will have the op

Biology, Chemistry, Biochemistry, or related field) OR relevant laboratory experience.

HydRegen in Oxford is seeking a Chemist to join our Chemistry R&D team.

If you are an ambitious scientist eager to apply your skills to one of the fastest-growing areas of sustainable materials innovation, we want to hear from you. We are seeking a Junior Research Scientist with a strong foundation in polymer or materials chemistry to join our growing R&D team. A&B Smar

A global biotechnology company is seeking a Medicinal Chemistry Research Scientist for an 18-month contract in Oxford.

The role supports a 5-year ERC Advanced Grant project focused on functional bilayers and nanoparticle systems, with a start in January 2027. Applicants must have a PhD in Chemistry (or near completion) and experience in functional bilayers, nanomaterials and extensive characterisation.

University of Oxford seeks a Postdoctoral Research Associate in functional polymer and synthetic host-guest chemistry for up to 4 years under Professors Davis and Langton.Based in the Department of Chemistry, Oxford, you will contribute to an ERC Advanced Grant project on hybrid nanoparticulate syst

The University of Oxford’s Department of Chemistry invites applications for a Postdoctoral Research Associate in functional polymer and synthetic host–guest chemistry, under the supervision of Professors Jason Davis and Matthew Langton, for up to four years.Experience in molecular synthesis, fun

Location: South Parks Road, Oxford, OX1 3QZ.Applications are invited for a Postdoctoral Research Associate in functional polymer and synthetic host-guest chemistry to work under the supervision of Professors Jason Davis and Matthew Langton for a period of up to 4 years.This exciting opportunity is p

Adecco is seeking a Registered Composition Data Support to join their EMEA Regulatory & Stewardship team in Milton, England.

Helio Display Materials Limited is seeking a laboratory technician or recent chemistry graduate to join our small-scale production team. You will work with senior chemists to support the pilot line, gain hands-on experience in materials synthesis, quality control, and scale-up of perovskite nanocrys

Working in a hands‑on laboratory environment, you'll be responsible for designing experiments, operating pressure reactors and delivering high-quality scientific data that supports product development and customer projects. A degree in Chemistry, Industrial Biotechnology, Engineering or a related

PhD, or equivalent industry experience, in Biochemistry, Chemistry, Chemical Biology, Bioengineering, Biotechnology or a related discipline.

At EIT, we are seeking a motivated, detail-focused Scientist, Biotechnology, to contribute to the early-stage development of a device-based metagenomic pathogen detection platform within EIT Oxford's Pathogen Programme. PhD, or equivalent industry experience, in Biochemistry, Chemistry, Chemical Bio

Location: South Parks Road, Oxford, OX1 3QZ.Applications are invited for a Postdoctoral Research Associate in functional polymer and synthetic host-guest chemistry to work under the supervision of Professors Jason Davis and Matthew Langton for a period of up to 4 years.This exciting opportunity is p

Biology Lead in Oxfordshire to steer discovery biology and plant science programmes. You will guide assay development, experimental design, and data-driven decisions while partnering with chemistry, project management and operations to ensure biology insights influence progression and portfolio deci

Job ID: 31155744Posted: Posted 29 Days AgoStart Date: 2026-07-16Location: United Kingdom - AbingdonTime Type: Full timeJOB DESCRIPTION:About AbbottAbbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.Abbott Toxicology is part of Abbott’s Rapid Diagnostics family of businesses. This role offers an opportunity to work for the UKs leading drug and alcohol testing provider.The Opportunity The position of Laboratory Project and Change Manager is a full-time, permanent position within our busy Laboratory Operations Department providing analytical toxicology services to numerous sectors, including law enforcement, maritime, drug treatment, and workplace drug testing.What you’ll do You will be responsible for delivering critical scientific and operational projects within the toxicology laboratory and an ongoing program of change. This is a vital role in delivering business transformation through in-depth understanding of our analytical processes and successful project management. You will bridge scientific expertise with structured project management and will require liaison with quality and commercial colleagues. This role is based on site at Abingdon Responsibilities Maintain a strategic view on all live / pipeline laboratory projects and change initiatives, ensuring alignment with business objectives and operational priorities. Maintain an up-to-date technical knowledge of toxicology and current analytical techniques and processes within screening, confirmation, data and result reporting Take ownership of laboratory change initiatives and drive end-to-end delivery via internal governance and change controls within the Quality Management System and Process Improvement Logs. Identify opportunities to improve laboratory workflows and operational efficiency through innovative thinking and the employment of Continuous Improvement methodologies and supportive frameworks (Lean, Six Sigma, automation, digitisation) to deliver an ongoing program of change.Lead, plan, execute and deliver laboratory scientific and operational projects:Produce project documentation in line with Toxicology portfolio requirementsDefine business case, scope and expected benefitsDevelop detailed project plans, timelines, schedules and tolerances, ensure adherence and be accountable for delivering within deadlinesIdentify and proactively manage risks, issues and dependenciesManage resource allocations and budget where appropriateTrack progress against milestones. Provide regular, transparent updates on progress, risks, and outcomes to the Laboratory Operations Director.Ensure engagement with teams across the business to manage stakeholder expectations, identify and understand dependencies, and ensure joined up commercial and operational delivery.Develop and deliver clear communication plans to support change adoption across the laboratory and business.Ensure changes deliver measurable improvements in performance, quality, or cost efficiencies. Quantify, track and report on benefits realised.Ensure effective implementation of change and transition from project into business-as-usual operations.Complete post implementation reviews of projects and change initiatives to ensure successful delivery has been achieved. Identify and capture lessons learned best practices for future change initiatives.Work closely with the Laboratory Operations Manager and Head of Scientific Services with change requirements required to meet departmental business objectives.What you will haveBSc Science degree in Analytical Chemistry, Toxicology, Pharmacology or related discipline, or equivalent laboratory experienceProven experience in project management, leading and implementing change initiatives to completionExperience working in a highly regulated environment, in accordance with documented Standard Operating Procedures and ISO 9001 and 17025 accreditations.IT literate with strong experience in Project, Word, Excel & Outlook.Preferred: -Lean practitioner or Six Sigma BeltAdvanced degrees or certifications (e.g., PMP, PRINCE2)Laboratory experience in analysis of drugs in biological samples using immunoassay screening and LCMS/MS Experience with LIMS or digital transformationExperience and Competencies Proven experience in change management, project management, or operational transformation within a highly regulated environmentStrong analytical and problem-solving abilities and the ability to interpret complex business needs and translate into operational requirements, Excellent understanding of continuous improvement concepts including Lean, Six Sigma, value stream mapping, 5S, Gemba and KaizenA ‘completer-finisher’ taking accountability for ideas from inception to delivery, in a highly regulated environment that requires robust metrics to confirm success.Excellent verbal and written communication skills and the ability to interact professionally with a diverse group of partners, senior managers, and subject matter experts.Ability to manage multiple complex projects and priorities simultaneously in line with business needs.The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted.JOB FAMILY:Operations QualityDIVISION:TOX ARDx ToxicologyLOCATION:United Kingdom > Abingdon : 21 Blacklands WayADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:NoMEDICAL SURVEILLANCE:Not ApplicableSIGNIFICANT WORK ACTIVITIES:Not Applicable

As a Chemist within HydRegen's Chemistry R&D team, you'll play a key role in developing, optimising and scaling catalytic hydrogenation processes. Chemist (Chemistry R&D) I Oxford I £40k - £50k. A degree in Chemistry, Industrial Biotechnology, Engineering or a related scientific discipline.

Applications are invited for a Postdoctoral Research Associate in functional bilayer chemistry to join the research group of Professor Jason Davis for a period of up to 3 years. Postdoctoral Research Associate in Chemistry. The research requires experience in functional bilayers, nanomaterials, thei

Postdoctoral Research Associate in functional polymer and synthetic host-guest chemistry. Applications are invited for a Postdoctoral Research Associate in functional polymer and synthetic host-guest chemistry to work under the supervision of Professors Jason Davis and Matthew Langton for a period o

PhD (pursuing or completed) in Chemistry, Chemical Engineering, Biochemistry, or related field. Remote contract for PhDs in Chemistry, Chemical Engineering, or related fields. Help fine-tune large language models (like ChatGPT) using your chemistry knowledge.

Location: 12 Mansfield Road, Oxford, OX1 3TA.Applications are invited for a Postdoctoral Research Associate in Artificial Molecular Machines to work under the supervision of Professor Matthew Langton for a period of up to 24 months.The project involves the synthesis of molecular machines capable of

University of Oxford Lifelong Learning is seeking Teaching Associates for the Astrophoria Foundation Year CEMS course in Oxford.The role is a part-time fixed-term contract, with hours varying by unit and term, ending on 31 July 2027 or 31 July 2028 depending on units taught.The post holder will prep

Applications are invited for the position of Postdoctoral Research Associate in Cyclocarbon Chemistry to work under the supervision of Professor Harry L. The project involves organic synthesis and is funded by the European Research Council. Find out more about the research group at:.

Exciting opportunity to join an innovative, industry leading laboratory equipment distributor to drive Sales in the South East. Our client is a leading provider of analytical instruments in the UK with products ranging from sample preparation systems to elemental analysis instrumentation. This opportunity calls for an ambitious scientist looking to drive sales whilst providing excellent service to customers. Within this role, you will support customers by identifying their key pain points and advising which products in your portfolio would best serve their requirements. Your position will focus on managing existing accounts and identifying new customers in academic, CRO, biotech and pharma laboratories. You will be based remotely and are expected to travel ~60% of your time to customer sites across the Southeast for instrument demonstrations, presentations and negotiation. To be considered for this position you will have: • BSc minimum in Chemistry or related subject, • Eligibility to work in the UK without sponsorship, • UK driver’s license and willingness to travel, • Proven experience within scientific sales and understanding of the sales process is highly desirable For your work you will be provided with a competitive basic salary, commission scheme, car and additional employee benefits. Please apply below to receive more details! Keywords: chemistry equipment, laboratory equipment, consumables sales, capital sales, business development, account management, sales, sales executive, technical sales, technical sales specialist, London, Cambridge, Oxford, Kent, Leicester, Northampton, Ipswich, St. Albans, Luton, Watford, VRS9389PC Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website