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We are currently recruiting for a Shift Microbiologist to join a leading pharmaceutical company in the Macclesfield area on a temporary contract. \n This is an excellent opportunity for an experienced microbiologist to work within a regulated pharmaceutical environment, supporting cleaning verification and validation activities and ensuring equipment meets the required microbiological and chemical cleanliness standards prior to release. \n The Role \n As a Shift Microbiologist, you will be responsible for carrying out and supporting routine microbiological activities associated with cleaning verification and validation activities. You will work closely with laboratory, manufacturing and quality teams to ensure sampling, testing and documentation are completed accurately and in accordance with GMP requirements. \n Key Responsibilities \n\n • Carry out visual inspections of equipment and manufacturing areas following cleaning activities.\n, • Perform swab sampling from predefined equipment and product-contact locations.\n, • Undertake rinse sampling where required as part of cleaning verification and validation activities.\n, • Support chemical residue testing, including checks for API, excipients, detergents and other relevant residues.\n, • Perform microbiological testing, including assessment of bioburden and, where applicable, endotoxin testing.\n, • Assess analytical and microbiological results against predefined acceptance criteria to determine whether equipment is suitable for release.\n, • Ensure sampling locations and methods are correctly documented and traceable.\n, • Complete and maintain cleaning records, sampling documentation and analytical results accurately and in a timely manner.\n, • Record, investigate and escalate deviations, atypical results and out-of-specification results in accordance with site procedures.\n, • Support the review and approval of cleaning verification and validation documentation.\n, • Ensure all activities are performed in accordance with GMP, SOPs, health and safety requirements and site quality standards.\n, • Work effectively as part of a shift-based team to support manufacturing operations.\n\n About You \n The successful candidate will ideally have: \n\n • A degree or equivalent qualification in Microbiology, Biological Sciences or a related discipline.\n, • Previous experience working within a pharmaceutical, biotechnology, healthcare or other GMP-regulated environment.\n, • Practical experience of microbiological sampling and testing.\n, • Experience with cleaning verification/validation would be highly advantageous.\n, • Knowledge of bioburden and/or endotoxin testing.\n, • An understanding of GMP requirements and good documentation practices.\n, • Strong attention to detail and a methodical approach to laboratory and sampling activities.\n, • The ability to accurately interpret results against defined acceptance criteria.\n, • Good communication and organisational skills.\n, • The flexibility to work within a shift-based environment.\n\n What's on Offer \n\n • Temporary contract with a leading pharmaceutical organisation.\n, • Opportunity to gain valuable experience within a highly regulated GMP environment.\n, • Exposure to cleaning verification and validation, microbiological testing and pharmaceutical manufacturing operations.\n, • Competitive hourly rate.\n, • Macclesfield-based position.\n\n If you are an experienced Microbiologist looking for your next opportunity within the pharmaceutical sector, we would be keen to hear from you.

Unfortunately, we are unable to offer visa sponsorship for this role. This is a full time, permanent position, working a flexible 36.5 hour week, Monday - Friday. We are recruiting for an enthusiastic and innovative Analytical Scientist for Eurofins at a client facility, a world-class pharmaceutical company based in Macclesfield. We have an opportunity for experienced Analytical Scientists with experience in drug substance development in the pharmaceutical industry. • You will act as the key point of contact for Eurofins clients, providing analytical testing expertise and subject matter knowledge across designated product areas., • You will use your analytical chemistry expertise to support global laboratories and external partners, ensuring the robustness, performance and compliance of analytical methods for drug substances., • You will coordinate analytical activities and support major change programmes and market access projects, working closely with cross-functional teams including Quality, Regulatory Affairs, Manufacturing and External Sourcing., • You will lead the transfer of commercial analytical methods to multiple laboratory locations, ensuring successful implementation and consistent operational standards., • You will collaborate with internal and external stakeholders to resolve technical challenges, drive continuous improvement and maintain regulatory compliance across analytical operations., • You will lead and develop a small team of analytical scientists, providing technical guidance, mentoring and support while contributing to international projects that may involve travel., • You will hold a degree, Master's degree or PhD in Chemistry, Pharmacy, Pharmaceutical Sciences or a related scientific discipline, with relevant post-graduate industry experience., • You will have proven experience in pharmaceutical analysis within a development laboratory environment, including leadership experience and the ability to guide technical teams., • You will have a strong understanding of chemical substance lifecycle management, from late-stage development through to commercial manufacture and ongoing product support., • You will have excellent project management, stakeholder engagement and influencing skills, with the ability to communicate effectively and collaborate across multiple functions., • You will have experience in data analysis and statistical interpretation, alongside extensive knowledge of analytical method development, optimisation, validation and transfer for release and stability testing., • You will have a thorough understanding of analytical techniques, root cause investigation, change assessment, SHE and cGMP requirements, with exposure to wider CMC disciplines, Quality, Regulatory Affairs and Manufacturing considered advantageous., • At Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events, and we are committed to charitable causes through global fundraising activities., • Reward and Recognition Scheme recognizing great work across our teams., • Holiday entitlement increases with service., • Option to opt into Health Cash Plan to help look after everyday health and wellbeing (claims for routine healthcare expenses)., • Life Assurance from day one (four times annual salary)., • Automatic enrolment into Company Pension Plan after three months (flexible to opt out)., • Access to Employee Assistance Programme (24/7 confidential support)., • Volunteering days program to support community involvement during working hours., • Free on-site car parking., • Opportunity to explore worldwide opportunities and access to Perkbox for savings and benefits. Our people are the backbone of what we do, so it's important we find the right individuals to join us. As a potential new recruit you may be invited to meet the team in an assessment centre or staged interview process depending on the role and its requirements. This will give you the opportunity to see what working for Eurofins is like and to showcase your key skills and strengths. #J-18808-Ljbffr

Join our expert team at AstraZeneca to pioneer a new future to meet global healthcare challenges. Be part of shaping a better future for all, supporting healthy communities by addressing the global societal and economic burden of disease. We are committed to leading in sustainability. Backed by a belief in the connection between the health of our business, people and the planet. In Chemical Development we believe that nothing is impossible, and we are determined to push the boundaries of science to deliver medicines to our patients. We combine people’s technical knowledge and understanding with their talent and drive to design, develop and optimise synthetic routes and processes that deliver the active pharmaceutical ingredients of our medicines in a sustainable, commercially viable way. We believe in innovation and continuous improvement, working closely with colleagues in academia and across industry, to ensure that we apply the cutting‑edge technologies and principles in the processes we develop. We have an exciting opportunity for a Senior Scientist to join the Automation & Data Science unit as a Laboratory Automation Scientist. The role will develop, deliver and support new automation platforms, while maintaining our growing fleet of automated and semi‑automated experimental equipment. This role is key to advance our Lab of the Future programme by enabling effective data generation and seamless data flows across the digital laboratory ecosystem. As part of a team of automation specialists, you will take ownership of a diverse range of laboratory instruments, ensuring their availability, performance and suitability for experimental workflows. You will troubleshoot and optimise existing systems while developing and deploying new automated workflows for wider departmental use. You will support the day-to-day activities of the laboratory facilities management team, ensuring that troubleshooting and routine laboratory housekeeping are completed effectively and in line with departmental requirements. As a key and central part of the Lab of the Future program, you will work in close partnership with chemists, engineers, data scientists, and IT, enabling data‑rich experimentation and smart process development. Your role encompasses hands‑on interaction with automation hardware/software, programming and troubleshooting systems, collaborating on integration projects, and ensuring solutions are robust and compliant with quality requirements. Drive the design, implementation, and integration of automated platforms for synthetic and analytical chemistry, ensuring efficiency from reagent management to data capture and modelling. Program and operate laboratory robotics, troubleshoot and resolve technical issues, and work closely with vendors and internal teams to optimize system performance. Lead or support technology evaluation, platform upgrades, and new automation initiatives that advance laboratory digital maturity. Train and empower laboratory scientists on use, maintenance, and best practice for new and existing automation systems. Ensure compliance with laboratory and IT quality standards, including software validation, change management, and system security and safety protocols. Ensure safe laboratory operations and prepare the required safety documentation. Streamline laboratory operations through the implementation of lab governance activities such as lab mapping, automated inventory tracking and QR‑enabled service‑request management. Execute practical experimental work on our automated platforms. This includes the execution of instrument testing protocols when designing new workflows or assuring data quality on new instrument investments. It may extend to provision of project data which feeds the development activities delivering new drug substance targets. Provide expert hands‑on support to the facilities management team delivering the MettlerToledo fleet maintenance. A degree (at PhD or lower-level with equivalent professional experience) in chemistry, chemical robotics or mechanical engineering, or a related technical field with hands‑on experience in laboratory or process automation. Proficiency in programming and scripting for automation platforms, robotics, and laboratory informatics. Experience with CAD and prototyping new tools and equipment Operational experience with laboratory automation systems, including design/development, troubleshooting, and optimization of robotic platforms. Proven record of innovation through, for instance, authorship of papers, inventor status on patents, or presenting at external conferences. The ability to develop and analyse multiple solutions to problems. Synthetic organic chemistry laboratory experience Experience within a process or manufacturing environment Familiarity with data science methodologies and AI/ML implementations in laboratory automation. Knowledge of GLS requirements for instrument maintenance Experience working with ALRs and HTE automated platforms Ability to challenge, innovate, think critically and flexibly, bringing new solutions and opportunities for chemical development. Excellent communication skills, with the ability to communicate across interfaces of scientific disciplines, culture, and expertise both internally and externally. The ability to confidently participate in, and potentially lead, improvement projects. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life‑changing medicines. In‑person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Here, your science moves with purpose. You will work with cutting‑edge biotechnology, new drug modalities, and rich data to shape how serious diseases are treated, including opportunities at the earliest stages where impact is greatest. We bring diverse experts together to spark bold ideas, apply innovative methods like AI and novel selection strategies, and learn quickly from real evidence. We value kindness alongside ambition, empowering you to take smart risks, collaborate deeply, and see your discoveries turn into medicines that reach patients. Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form. #J-18808-Ljbffr

Macclesfield At AstraZeneca, we are driven by our commitment to deliver accelerated growth and to make people's lives better. We thrive in our often intense and ambiguous environment, seeking out new challenges and working towards new solutions. We are part of an inclusive and giving community, supporting each other on our journeys. We are leading the way in delivering Lean processes that drive greater efficiency and speed. Sustainable practices are at the heart of what we do, ensuring we manage our environmental impact across all our activities and products. We are now looking for a Capital Project & High-Hazard Lead to join the team! To hold the single coordination point for capital projects, CDM duties, permit-to-work system integrity, and high-hazard work assurance across the Macclesfield Campus. The role carries the relationship, coordination, and assurance layer for Principal Contractor liaison, CDM duty-holder support, permit-system integrity, and high-risk operational work governance, operating the AI toolset that handles workflow administration and document register maintenance. • Hold the Campus permit-to-work system integrity assurance — system design, deviation governance, audit response and cultural engagement., • Lead the Campus CDM duty-holder coordination — Principal Designer and Principal Contractor liaison, HSE F10 notification governance, designer risk assessment integration., • Own the contractor competency framework — pre-qualification matrix, on-site induction governance, named-individual competency verification., • Coordinate the capital project Safety, Health and Environment (SHE) interface — project-stage SHE inputs, design risk assessment, pre-commissioning SHE assurance., • Provide assurance on high-risk operational work — energy isolation, lockout / tagout, confined space, working at height., • Operate the AI-supported permit lifecycle workflow, CDM document register, and contractor competency tracker as the named operating-user., • Cross-pillar collaboration with the Associate Director - Site Safety Operations & Resilience on high-hazard work and emergency response interfaces., • Lead permit-system audit response — internal audit findings, AstraZeneca Global audit visits, EA and HSE inspection close-out., • Own the CDM, permit-to-work, and high-hazard operational work training programme — curriculum for permit issuers and acceptors, contractor competency inductions, refresher cycles., • Provide SHE assurance on the Engineering-owned statutory inspection regimes — LOLER (lifting), PUWER (work equipment), electrical safety rules and Authorised Person regime., • Own the waste contractor audit programme on capital projects and decommissioning / demolition governance (with Associate Director - SHE Regulated Operations on waste routing)., • AstraZeneca Pharma capital project SHE peer-network participation., • External representation in CDM and permit-system industry forums to support the development of best practice and process optimisation., • Cross-departmental advice to operations teams on permit and high-hazard work., • Support to Director – SHE people, Workplace & Capital on capital project SHE governance., • Degree qualified in engineering, construction management, or related field (or equivalent relevant professional qualification and/or experience), • CDM Principal Designer / CDM Principal Contractor experience., • Significant experience in capital project SHE or high-hazard permit-to-work coordination., • Strong working knowledge of UK CDM 2015 and PUWER regulations., • Track record of contractor management at major industrial sites., • Pharmaceutical or specialty chemical industry experience., • NEBOSH Construction Certificate., • Experience of AI-enabled permit-system tools., • Project SHE assurance framework experience. Applications close midnight Wednesday 7th October Please note that interviews for this role are likely to commence 14th October 2026 At AstraZeneca, we are leading our Operations function at an exciting time of growth and evolution. We pioneer new approaches and processes across our sites, empowering our teams to foster a Lean mindset and sustainable practices. Every change we make is to deliver better outcomes for our patients. We are the champions of Lean, ensuring our teams understand and embody the benefits it can bring. There's improved quality and safety, as well as speed. Our manufacturing sites are environments of constant and rapid change. It's a place to expect the unexpected. There's rarely an obvious answer to the varied challenges we face, so it takes adaptability, flexibility and patience to thrive here. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. Ready to take the next step in your career? 25-Sept-2026 07-Oct-2026 Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form. #J-18808-Ljbffr

Capital Project & High-Hazard Lead Macclesfield At AstraZeneca, we are driven by our commitment to deliver accelerated growth and to make people's lives better. We thrive in our often intense and ambiguous environment, seeking out new challenges and working towards new solutions. We are part of an inclusive and giving community, supporting each other on our journeys. We are leading the way in delivering Lean processes that drive greater efficiency and speed. Sustainable practices are at the heart of what we do, ensuring we manage our environmental impact across all our activities and products. We are now looking for a Capital Project & High-Hazard Lead to join the team! Introduction to Role To hold the single coordination point for capital projects, CDM duties, permit-to-work system integrity, and high-hazard work assurance across the Macclesfield Campus. The role carries the relationship, coordination, and assurance layer for Principal Contractor liaison, CDM duty-holder support, permit-system integrity, and high-risk operational work governance, operating the AI toolset that handles workflow administration and document register maintenance. Accountabilities • Hold the Campus permit-to-work system integrity assurance — system design, deviation governance, audit response and cultural engagement., • Lead the Campus CDM duty-holder coordination — Principal Designer and Principal Contractor liaison, HSE F10 notification governance, designer risk assessment integration., • Own the contractor competency framework — pre-qualification matrix, on-site induction governance, named-individual competency verification., • Coordinate the capital project Safety, Health and Environment (SHE) interface — project-stage SHE inputs, design risk assessment, pre-commissioning SHE assurance., • Provide assurance on high-risk operational work — energy isolation, lockout / tagout, confined space, working at height., • Operate the AI-supported permit lifecycle workflow, CDM document register, and contractor competency tracker as the named operating-user., • Cross-pillar collaboration with the Associate Director - Site Safety Operations & Resilience on high-hazard work and emergency response interfaces., • Lead permit-system audit response — internal audit findings, AstraZeneca Global audit visits, EA and HSE inspection close-out., • Own the CDM, permit-to-work, and high-hazard operational work training programme — curriculum for permit issuers and acceptors, contractor competency inductions, refresher cycles., • Provide SHE assurance on the Engineering-owned statutory inspection regimes — LOLER (lifting), PUWER (work equipment), electrical safety rules and Authorised Person regime., • Own the waste contractor audit programme on capital projects and decommissioning / demolition governance (with Associate Director - SHE Regulated Operations on waste routing)., • AstraZeneca Pharma capital project SHE peer-network participation., • External representation in CDM and permit-system industry forums to support the development of best practice and process optimisation., • Cross-departmental advice to operations teams on permit and high-hazard work., • Support to Director – SHE people, Workplace & Capital on capital project SHE governance. Essential Skills & Experience • Degree qualified in engineering, construction management, or related field (or equivalent relevant professional qualification and/or experience), • CDM Principal Designer / CDM Principal Contractor experience., • Significant experience in capital project SHE or high-hazard permit-to-work coordination., • Strong working knowledge of UK CDM 2015 and PUWER regulations., • Track record of contractor management at major industrial sites. Desirable Skills & Experience • Pharmaceutical or specialty chemical industry experience., • NEBOSH Construction Certificate., • Experience of AI-enabled permit-system tools., • Project SHE assurance framework experience. Applications close midnight Wednesday 7th October Please note that interviews for this role are likely to commence 14th October 2026 At AstraZeneca, we are leading our Operations function at an exciting time of growth and evolution. We pioneer new approaches and processes across our sites, empowering our teams to foster a Lean mindset and sustainable practices. Every change we make is to deliver better outcomes for our patients. We are the champions of Lean, ensuring our teams understand and embody the benefits it can bring. There's improved quality and safety, as well as speed. Our manufacturing sites are environments of constant and rapid change. It's a place to expect the unexpected. There's rarely an obvious answer to the varied challenges we face, so it takes adaptability, flexibility and patience to thrive here. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. Ready to take the next step in your career? Date Posted 25-Sept-2026 Closing Date 07-Oct-2026Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form. #J-18808-Ljbffr

Are you experienced in instrumentation calibration and looking for a varied field and workshop-based role where you can work with process instrumentation across a wide range of customer sites? If you’ve also worked in the following roles, we’d also like to hear from you: Calibration Technician, Field Service Engineer, Calibration Engineer, Instrumentation Technician, Service Engineer, Field Technician, Instrument Technician, Process Instrumentation Technician SALARY: £32,000 - £40,000 per annum (depending on experience) + Car + Fuel Card + Benefits (see below) LOCATION: North West Region / Field Based with occasional trips covering the whole of England and the Continent JOB TYPE: Full-Time, Permanent WORKING HOURS: Full-Time, Permanent This is an excellent opportunity for a Field Calibration Technician to join a growing organisation providing calibration, service and repair support for sophisticated process instrumentation. As the Field Calibration Technician you will work across customer sites and workshop environments, carrying out field and workshop calibrations, preparing service reports and test certificates, and supporting clients across a range of industrial sectors. The Field Calibration Technician will need strong instrumentation calibration experience, excellent communication skills and the ability to build positive working relationships with customers while managing a varied workload. Your duties as the Field Calibration Technician include: • Carry Out Calibration Work: Complete field and workshop calibrations on process instrumentation, • Service and Repair Equipment: Provide calibration service and repair support for process instrumentation, • Support Customer Sites: Work in the field across customer locations, with occasional travel across Great Britain and the Continent, • Prepare Documentation: Raise accurate service reports and test certificates following completed work, • Build Client Relationships: Develop positive working relationships with customers while representing the organisation professionally on site, • Balance Field and Workshop Work: Work across both field-based assignments and workshop or office-based activity, • Instrumentation calibration experience in one or more relevant sectors, such as chemical, life sciences, power, food, steel, water, wastewater, paper, oil and gas, or petrochemical, • Full driving licence, • Highly self-motivated with the ability to work on your own initiative and as part of a team, • Flexible approach to working activities, • Excellent verbal and written communication skills, • Confident, assertive and professional approach, • Ability to develop good working relationships with customers, • Good organisational skills, • Excellent punctuality and timekeeping, • Ideally qualified to ONC / HNC level, preferably in Electronics or Instrumentation and Control, • Field-based or customer-facing experience, • CCNSG Card, • CompEx 1-4 / 1-6, • Experience within process and/or petrochemical environments, • Electrical and controls knowledge, • Profibus knowledge, • UKAS knowledge, • Salary package of £32,000 - £40,000 per annum, depending on experience, • Fully funded car and tech, • Fuel card, including allowances for breakfast, lunch and dinner when working away, • Paid overnight allowance for every night spent working away, • Employee training and development opportunities, • Company events, • Free gym membership close to the HQ office, • Company pension package, • Total holiday package of 31 days, • Employer-sponsored office attire, • Employer-funded cash plan covering costs such as opticians, dentist, physiotherapy and more, • Free on-site parking with electric / plug-in charging points, • Christmas shutdown JOB REF: AWDO-P15055 #J-18808-Ljbffr

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Eurofins PSS Insourcing Solutions® is a global, award-winning insourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client’ site, utilising their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility. If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions® is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries! We’re proud to be an armed forces-friendly place to work and welcome applications from reservists, armed forces veterans (including the wounded, injured and sick), as well as cadet instructors, and military spouses and partners. Unfortunately, we are unable to offer visa sponsorship for this role. This is a full time, permanent position, working a flexible 36.5 hour week, Monday – Friday. We are currently recruiting for an experienced, enthusiastic and innovative PAT Scientist. This is an exciting opportunity based at our client’s facility, a world class Pharmaceutical company based in Macclesfield. You will have a proven track record of delivering in-line and at-line analytical technology to pharmaceutical development projects and collaborating with project scientists to help support key Client projects. Job Responsibilities that you be covering: • You will provide real-time laboratory data analytics to support process chemistry activities, delivering high-density insights that enable accelerated process understanding and decision-making., • You can expect to collaborate closely with chemists and engineers to develop and implement Process Analytical Technology (PAT) solutions for complex drug substance projects, ensuring delivery against project milestones across early to late-stage development with reaction monitoring as well as continuous manufacturing., • You will utilise reaction monitoring and continuous manufacturing strategies to generate meaningful scientific insights that support client project requirements and drive successful outcomes., • The successful applicant will provide scientific and technical leadership within PAT, solving complex challenges, identifying key learnings, and sharing best practices across the wider department., • You canexpecttodemonstrate ownership of PAT strategy and development on drug substance projects, representing Chemical Development as required and providing expert challenge to enhance project delivery and innovation., • You will contribute to the ongoing development of Chemical Development capabilities by supporting current and future client portfolios, driving continuous improvement initiatives, and promoting new ways of working and scientific advancement. What skills, qualifications and experiences you will hold as an Medical Device Development Specialist: • You will hold a BSc, MSc or PhD in a relevant scientific discipline, with experience gained within Research & Development, manufacturing, academia, or the chemical and pharmaceutical industries., • You will have significant experience working within chemical or analytical laboratory environments, supporting analytical development for Active Pharmaceutical Ingredients (APIs) using techniques such as UPLC, GC and Karl Fischer analysis., • You will be expected to have practical expertise in Process Analytical Technology (PAT) and one or more key spectroscopic or analytical techniques, including NIR, Raman, IR, UV or LC, enabling you to provide specialist guidance to project teams., • You will have experience working with PAT applications in drug substance development, with exposure to quantitative model development, real-time process monitoring, and ideally scale-up activities within clinical or commercial manufacturing environments., • You will hold coding experience in Matlab, Python or similar programming languages, alongside a strong data-centric mindset and a willingness to further develop expertise in chemometrics and advanced data analysis., • You will have experience operating within GMP-regulated environments and a sound understanding of Safety, Health and Environmental (SHE) principles, demonstrating a commitment to maintaining the highest standards of compliance and safety. At Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events, and we are committed to charitable causes through global fundraising activities. As a Eurofins employee you will benefit from: • Being part of a Reward and Recognition Scheme, recognising great work across our teams., • Holiday entitlement increases with service., • The option to opt into our Health Cash Plan, designed to help look after your everyday health and wellbeing. This allows you to claim back the cost of routine healthcare expenses such as dental check-ups, eye tests, glasses or contact lenses and other everyday medical treatments., • Life Assurance from day one, providing cover of four times your annual salary., • Automatic enrolment into our Company Pension Plan after three months (with the flexibility to opt out if you choose), • Access to our Employee Assistance Programme, offering 24/7 confidential support for both personal and work-related matters., • Being able to register your interest in volunteering days, which are designed to support employees who wish to do voluntary work during working hours as part of a wider strategy to contribute positively to the local community., • Free on-site car parking., • The opportunity to explore worldwide opportunities., • Everyone who joins our team also gets access to Perkbox, allowing you to save money all year round. Whether its supermarket savings or days out, the daily coffee or a summer holiday – there’s something to suit everyone’s lifestyle. What Happens Next Our people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths. As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. #J-18808-Ljbffr

Macclesfield, UK The Macclesfield Campus is an essential part of AstraZeneca’s UK Operation and the 2nd largest operational site within the company’s global network. It is approx. 100 acres with around 4500 people working on site. The site is unique in the AstraZeneca network having Operations, R&D, G&A, IT and others on its site. £28,000 Base Salary, Bonus & Flexible Benefit AstraZeneca is a global, science-led, patient-centred biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious disease. But we’re more than a global leading pharmaceutical company. At AstraZeneca, we are dedicated to being a Great Place to Work where you are empowered to push the boundaries of science and fuel your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. Join a Truly Inclusive and Supportive International Team. As an AstraZeneca placement student, there is a huge network of support available to you. You’ll have a dedicated supervisor, a supportive early talent peer network, and a variety of Employee Resource Groups you can join. We help and empower each other, and our supervisors are committed to providing you with all the guidance and support you need to build your skills, confidence and capabilities. Whatever your background and experience, you will be welcomed and encouraged to speak up, ask questions and share knowledge. You will be a valued part of an international team of truly supportive, collaborative and inclusive individuals. The successful role holder will work in Global Product Development, working in a Process Engineering groups and alongside multidisciplinary teams, responsible for the application of new technologies, process development and safe manufacturing scale up, leading to right first-time campaigns. Global Product Development is responsible for the formulation design, manufacturing process development, and optimisation of drug products. This includes a variety of dosage forms such as tablets and capsules as well injectable and inhalation-based products. The one-year industrial student placement will offer a mixture of drug development project work and/or a new technology project with support from an experienced engineer. In Global Product Development, experiences will involve laboratory work and simulation of unit operations such as feeding, blending, filling and tablet compression, primarily centred on the ongoing development of our continuous manufacturing capability. • Currently undertaking an undergraduate or integrated master’s degree with the opportunity to spend 1 year in industry starting in September 2027., • Degree subject within a Chemical, or Process Engineering discipline., • Strong planning and organisation skills., • Ability to see opportunities, learn, and apply that learning to drive innovation with good collaboration and teamworking skills., • Confident communicating with a wide range of stakeholders., • Competent in the use of coding and modelling packages such as Python, MATLAB, Aspen, gProms, Ansys CFD. Applications Open: 4th September 2026 Applications Close: 2nd October 2026 Assessment Day: 6th November 2026 Start Date: 7th September 2027 This position is a 12-month fixed term contract. AstraZeneca is proud to be ranked as a Top 100 ‘Best Student Employer’ in the UK by RateMyPlacement. Browse our reviews here (link) AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. Date Posted: 08-Sept-2026 Closing Date: 02-Oct-2026 Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form. #J-18808-Ljbffr

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Eurofins PSS Insourcing Solutions® is a global, award-winning insourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client’ site, utilising their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility. If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions® is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries! We’re proud to be an armed forces-friendly place to work and welcome applications from reservists, armed forces veterans (including the wounded, injured and sick), as well as cadet instructors, and military spouses and partners. If you want to continue to help make our world a safer and healthier place, then apply for the role below and become a part of the extraordinary Eurofins network Unfortunately, we are unable to offer visa sponsorship for this role. This is a full time, permanent position, working a flexible 36.5 hour week, Monday – Friday. We are currently recruiting for an experienced, enthusiastic and innovative PAT Scientist. This is an exciting opportunity based at our client’s facility, a world class Pharmaceutical company based in Macclesfield. You will have a proven track record of delivering in-line and at-line analytical technology to pharmaceutical development projects and collaborating with project scientists to help support key Client projects. • You will provide real-time laboratory data analytics to support process chemistry activities, delivering high-density insights that enable accelerated process understanding and decision-making., • You can expect to collaborate closely with chemists and engineers to develop and implement Process Analytical Technology (PAT) solutions for complex drug substance projects, ensuring delivery against project milestones across early to late-stage development with reaction monitoring as well as continuous manufacturing., • You will utilise reaction monitoring and continuous manufacturing strategies to generate meaningful scientific insights that support client project requirements and drive successful outcomes., • The successful applicant will provide scientific and technical leadership within PAT, solving complex challenges, identifying key learnings, and sharing best practices across the wider department., • You can expect to demonstrate ownership of PAT strategy and development on drug substance projects, representing Chemical Development as required and providing expert challenge to enhance project delivery and innovation., • You will contribute to the ongoing development of Chemical Development capabilities by supporting current and future client portfolios, driving continuous improvement initiatives, and promoting new ways of working and scientific advancement., • You will hold a BSc, MSc or PhD in a relevant scientific discipline, with experience gained within Research & Development, manufacturing, academia, or the chemical and pharmaceutical industries., • You will have significant experience working within chemical or analytical laboratory environments, supporting analytical development for Active Pharmaceutical Ingredients (APIs) using techniques such as UPLC, GC and Karl Fischer analysis., • You will be expected to have practical expertise in Process Analytical Technology (PAT) and one or more key spectroscopic or analytical techniques, including NIR, Raman, IR, UV or LC, enabling you to provide specialist guidance to project teams., • You will have experience working with PAT applications in drug substance development, with exposure to quantitative model development, real-time process monitoring, and ideally scale-up activities within clinical or commercial manufacturing environments., • You will hold coding experience in Matlab, Python or similar programming languages, alongside a strong data-centric mindset and a willingness to further develop expertise in chemometrics and advanced data analysis., • You will have experience operating within GMP-regulated environments and a sound understanding of Safety, Health and Environmental (SHE) principles, demonstrating a commitment to maintaining the highest standards of compliance and safety. At Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events, and we are committed to charitable causes through global fundraising activities. • Being part of a Reward and Recognition Scheme, recognising great work across our teams., • Holiday entitlement increases with service., • The option to opt into our Health Cash Plan, designed to help look after your everyday health and wellbeing. This allows you to claim back the cost of routine healthcare expenses such as dental check-ups, eye tests, glasses or contact lenses and other everyday medical treatments., • Life Assurance from day one, providing cover of four times your annual salary., • Automatic enrolment into our Company Pension Plan after three months (with the flexibility to opt out if you choose), • Access to our Employee Assistance Programme, offering 24/7 confidential support for both personal and work-related matters., • Being able to register your interest in volunteering days, which are designed to support employees who wish to do voluntary work during working hours as part of a wider strategy to contribute positively to the local community., • Free on-site car parking., • The opportunity to explore worldwide opportunities., • Everyone who joins our team also gets access to Perkbox, allowing you to save money all year round. Whether its supermarket savings or days out, the daily coffee or a summer holiday – there’s something to suit everyone’s lifestyle. Our people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths. As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations. Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. For more information about Eurofins PSS® please visit our website and watch a message below from our Global Head, Beth Di Paolo. #J-18808-Ljbffr

Join our expert team at AstraZeneca to pioneer a new future to meet global healthcare challenges. Be part of shaping a better future for all, supporting healthy communities by addressing the global societal and economic burden of disease. We are committed to leading in sustainability. Backed by a belief in the connection between the health of our business, people and the planet. In Chemical Development we believe that nothing is impossible, and we are determined to push the boundaries of science to deliver medicines to our patients. We combine people’s technical knowledge and understanding with their talent and drive to design, develop and optimise synthetic routes and processes that deliver the active pharmaceutical ingredients of our medicines in a sustainable, commercially viable way. We believe in innovation and continuous improvement, working closely with colleagues in academia and across industry, to ensure that we apply the cutting‑edge technologies and principles in the processes we develop. We have an exciting opportunity for a Senior Scientist to join the Automation & Data Science unit as a Laboratory Automation Scientist. The role will develop, deliver and support new automation platforms, while maintaining our growing fleet of automated and semi‑automated experimental equipment. This role is key to advance our Lab of the Future programme by enabling effective data generation and seamless data flows across the digital laboratory ecosystem. As part of a team of automation specialists, you will take ownership of a diverse range of laboratory instruments, ensuring their availability, performance and suitability for experimental workflows. You will troubleshoot and optimise existing systems while developing and deploying new automated workflows for wider departmental use. You will support the day‑to‑day activities of the laboratory facilities management team, ensuring that troubleshooting and routine laboratory housekeeping are completed effectively and in line with departmental requirements. In your role you will identify and compare existing capabilities, develop or configure prototypes, and pilot the preferred approach with selected teams. Following a successful pilot, the role holder will support the handover to the chemistry/analytical teams. As a key and central part of the Lab of the Future program, you will work in close partnership with chemists, engineers, data scientists, and IT, enabling data‑rich experimentation and smart process development. Your role encompasses hands‑on interaction with automation hardware/software, programming and troubleshooting systems, collaborating on integration projects, and ensuring solutions are robust and compliant with quality requirements. • Drive the design, implementation, and integration of automated platforms for synthetic and analytical chemistry, ensuring efficiency from reagent management to data capture and modelling., • Translating analytical workflows into practical, user‑centred automation solutions, supporting a wide range of technical areas from sample preparation to various analytical techniques, such as chromatography and spectroscopies/spectrometries., • Program and operate laboratory robotics, troubleshoot and resolve technical issues, and work closely with vendors and internal teams to optimize system performance., • Lead or support technology evaluation, platform upgrades, and new automation initiatives that advance laboratory digital maturity., • Train and empower laboratory scientists on use, maintenance, and best practice for new and existing automation systems., • Ensure compliance with laboratory and IT quality standards, including software validation, change management, and system security and safety protocols., • Ensure safe laboratory operations and prepare the required safety documentation., • Streamline laboratory operations through the implementation of lab governance activities such as lab mapping, automated inventory tracking and QR‑enabled service‑request management., • Execute practical experimental work on our automated platforms. This includes the execution of instrument testing protocols when designing new workflows or assuring data quality on new instrument investments. It may extend to provision of project data which feeds the development activities delivering new drug substance targets., • Provide expert hands‑on support to the facilities management team delivering the MettlerToledo fleet maintenance., • A degree (at PhD or lower-level with equivalent professional experience) in chemistry, chemical robotics or mechanical engineering, or a related technical field with hands‑on experience in laboratory or process automation., • Proficiency in programming and scripting for automation platforms, robotics, and laboratory informatics., • Experience with CAD and prototyping new tools and equipment, • Operational experience with laboratory automation systems, including design/development, troubleshooting, and optimization of robotic platforms., • Proven record of innovation through, for instance, authorship of papers, inventor status on patents, or presenting at external conferences., • The ability to develop and analyse multiple solutions to problems., • Synthetic organic chemistry laboratory experienceand/or experience working in analytical laboratories and experience of chromatography or spectroscopic characterisation techniques e.g. UHPLC, NMR, MS, • Experience within a process or manufacturing environment, • Experience from working with automated analytical procedures, • Experience of the analytical area such as method development and method validation., • Familiarity with data science methodologies and AI/ML implementations in laboratory automation., • Knowledge of GLS requirements for instrument maintenance, • Experience working with ALRs and HTE automated platforms, • Ability to challenge, innovate, think critically and flexibly, bringing new solutions and opportunities for chemical development., • Excellent communication skills, with the ability to communicate across interfaces of scientific disciplines, culture, and expertise both internally and externally., • The ability to confidently participate in, and potentially lead, improvement projects. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life‑changing medicines. In‑person working gives us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Here, your science moves with purpose. You will work with cutting‑edge biotechnology, new drug modalities, and rich data to shape how serious diseases are treated, including opportunities at the earliest stages where impact is greatest. We bring diverse experts together to spark bold ideas, apply innovative methods like AI and novel selection strategies, and learn quickly from real evidence. We value kindness alongside ambition, empowering you to take smart risks, collaborate deeply, and see your discoveries turn into medicines that reach patients. Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form. #J-18808-Ljbffr

We are currently recruiting for a Shift Microbiologist to join a leading pharmaceutical company in the Macclesfield area on a temporary contract. This is an excellent opportunity for an experienced microbiologist to work within a regulated pharmaceutical environment, supporting cleaning verification and validation activities and ensuring equipment meets the required microbiological and chemical cleanliness standards prior to release. As a Shift Microbiologist, you will be responsible for carrying out and supporting routine microbiological activities associated with cleaning verification and validation activities. You will work closely with laboratory, manufacturing and quality teams to ensure sampling, testing and documentation are completed accurately and in accordance with GMP requirements. • Carry out visual inspections of equipment and manufacturing areas following cleaning activities., • Perform swab sampling from predefined equipment and product-contact locations., • Undertake rinse sampling where required as part of cleaning verification and validation activities., • Support chemical residue testing, including checks for API, excipients, detergents and other relevant residues., • Perform microbiological testing, including assessment of bioburden and, where applicable, endotoxin testing., • Assess analytical and microbiological results against predefined acceptance criteria to determine whether equipment is suitable for release., • Ensure sampling locations and methods are correctly documented and traceable., • Complete and maintain cleaning records, sampling documentation and analytical results accurately and in a timely manner., • Record, investigate and expand deviations, atypical results and out-of-specification results in accordance with site procedures., • Support the review and approval of cleaning verification and validation documentation., • Ensure all activities are performed in accordance with GMP, SOPs, health and safety requirements and site quality standards., • Work effectively as part of a shift-based team to support manufacturing operations. The successful candidate will ideally have: • A degree or equivalent qualification in Microbiology, Biological Sciences or a related discipline., • Previous experience working within a pharmaceutical, biotechnology, healthcare or other GMP-regulated environment., • Practical experience of microbiological sampling and testing., • Experience with cleaning verification/validation would be highly advantageous., • Knowledge of bioburden and/or endotoxin testing., • An understanding of GMP requirements and good documentation practices., • Strong attention to detail and a methodical approach to laboratory and sampling activities., • The ability to accurately interpret results against defined acceptance criteria., • Good communication and organisational skills., • The flexibility to work within a shift-based environment., • Temporary contract with a leading pharmaceutical organisation., • Opportunity to gain valuable experience within a highly regulated GMP environment., • Exposure to cleaning verification and validation, microbiological testing and pharmaceutical manufacturing operations., • Competitive hourly rate., • Macclesfield-based position. If you are an experienced Microbiologist looking for your next opportunity within the pharmaceutical sector, we would be keen to hear from you. #J-18808-Ljbffr

Role: Enterprise Process Lead – Asset Management & Compliance Role Type: Temporary – 12 Months Location: Macclesfield – x3 Days working on-site / x2 remote Your New Company The Axial Programme will be powered by S/4HANA a new ERP (Enterprise Resource Planning) system which will be implemented right across the organisation and will provide our business with standardised processes, enhanced financial management, common data and real time reporting, transforming the way we work through our entire supply chain - from bench to patient. Our current technology is used by more than 20,000 employees daily, is foundational to all AZ entities and is central to most core business processes. This programme provides the opportunity for real transformation and to shape the way of working globally for many years to come. We now have an opportunity for an Enterprise Process Lead – Asset Management & Product Compliance to join the programme, working within the Production to Dispatch Door process area. Your New Role As EPL, you will be accountable for transforming the Asset Management approach to ensure effective deployment of our SAP (S4/HANA) solution across our Internal Sites. You will lead a team of SMEs in the definition, design and ongoing improvement of the processes and tools to ensure efficient, effective and transparent ways of working. This will include all forms of Asset Management within the Global Operations Network, collaborating with existing Process Areas (such as Total Productive Maintenance) and partnering with External Providers where appropriate. The role will also provide leadership to the Product Compliance Team ensuring we deliver our SHE (safety, health and environment) requirements for to comply with Dangerous Goods Shipping and creation/maintenance of our Product Safety Data Sheets. You will be aligned to the ‘Production To Dispatch Door’ Enterprise Process, with a strong focus on the optimisation of Assets throughout their lifecycle but support other process areas as appropriate. Underpinned by a culture of continuous improvement, the defined Asset Management processes will drive improvements in efficiency and effectiveness to support the Internal Manufacturing Capability. You will contribute to setting the strategic direction for the process with the Executive Process Owner (EPO) and drive the process towards that strategic direction. You will ensure you are not just defining the Asset Management Capabilities to support our Business today, but enabling our future needs as part of Ambition 2030 and aligned to our acceleration towards Smart Factories. Main Responsibilities: • Lead the SAP S/4HANA Programme activities for the Asset Management Business Processes including defining the next phase of the “Global Template” and collaborating with the next sites as we educate and develop their capabilities in readiness for deployment., • Lead a team of Experts to define Globally standardised and repeatable processes (in collaboration with the BAU BPO) adopting standard use of S/4 HANA within the Asset Management area, minimising the need for Local Technical and/or Process Customisation, • Network with colleagues across the Business to identify improvement opportunities, with a focus on driving forward the Lean journey through supporting the Total Productive Maintenance Framework, • Ensure Future State Processes enable AstraZeneca to meet all applicable Regulatory Standards, e.g. SHE, GxP, SOX, Accounting GAAP etc, • Champion new strategies to improve Business Processes with the BAU BPO and ensure Business Continuity, meeting current and future Business requirements, • Collaborate with the Programme and Business Data Teams to define the Data requirements for the Processes, Analytics and Reporting, • Create and sustain key artefacts required to develop a successful transition to the next generation SAP ERP including the End-to-End Process Maps, Roles Descriptors and Process Controls, • Ensure that Non-SAP System requirements are understood and considered in the Process and Data Designs, • Establish and actively manage relationships with diverse pools of key partners throughout AstraZeneca to ensure commitment and understanding to Programme Objectives, • Establish and implement Key Performance Indicators to drive forward Asset efficiency and effectiveness, • Similarly, provide leadership to the Product Compliance Team ensuring we deliver our SHE (safety, health and environment) requirements for to comply with Dangerous Goods Shipping and creation/maintenance of our Product Safety Data Sheets., • Extensive experience of Asset Lifecycle Management processes and specifically SAP Plant Maintenance processes., • Detailed understanding of Asset Management Master Data requirements, • Demonstrated ability to influence key Partner Groups across Multiple Locations and/or External Parties, • Demonstrated ability to successfully deliver Engineering and/or IT Change across Multiple Locations and/or Business Functions, • Strong Communication and Relationship Building skills with an ability to Influence others to achieve Objectives, • Ability to interpret and communicate Technical information into Business language, • Similarly, the leadership capability/leadership acumen to provide leadership to the Product Compliance Team ensuring we deliver our SHE (safety, health and environment) requirements., • Bachelor of Engineering/Science in an appropriate field Desirable for the role • Knowledge of SHE (safety, health and environment) requirements for to comply with Dangerous goods shipping and creation/maintenance of our Product safety data sheets., • Experience of SHE Management processes including chemical regulatory controls/product safety processes; ideally experienced in SAP-EHS/Product Safety and Stewardship module or equivalent., • Understanding of SHE Management Master Data requirements WHY ASTRAZENECA? It's an exciting time to join AstraZeneca, a global business that's rapidly growing - there's a lot happening and even more to come. And we are a valued part of this journey. Respected partners across the business, we provide the platform that's going to power us to achieve more. So, what's next? Are you ready to bring new insights and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours. Please apply with a copy of your CV. #J-18808-Ljbffr

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