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Procurement Manager Flexible location (Selby, North Yorkshire or Glasgow preferred) Full time, permanent Hybrid working Closing date: Monday 2nd March 2026 Who we are: We’re not just talking about making a difference, we’re making it happen. We generate dispatchable, renewable power and create stable energy in an uncertain world. Building on our proud heritage, we have ambition to become the global leader in sustainable biomass and carbon removals. About the role: As an experienced procurement professional, you’ll thrive in a busy commercial environment. You'll build meaningful and strong relationships with internal and external stakeholders to drive procurement excellence at every stage of the process. This is a fast-paced role, which requires attention to detail and working to tight deadlines. Ensuring compliance to policies and processes will enable you to drive improved commercial outcomes and to deliver results that support the overall procurement strategy here at Drax. As a senior member of a transformative team you’ll help drive the successful delivery of the overall procurement team goals. Day-to-day you'll be responsible for all aspects of the Source to Contract cycle while considering risk and cost. You’ll play a key role in the development and implementation of sourcing strategies to maximise value whilst ensuring the right level of governance is applied. You’ll also provide day to day procurement guidance and advice to other team members. Building new relationships and working with a wide range of internal customers will be the key to success in this role. You’ll work closely with the wider procurement team, to ensure continuous improvement and best practice is shared throughout the team to optimise performance. Drax is committed to developing its colleagues and investing in your continuing professional development we are happy to support World Contracting & Commerce training and certification (previously IACCM) and CIPS membership. Who we’re looking for: You’ll have strong technical procurement skills, ideally with Mechanical, Electrical and Civils works category experience and understanding of best practice. Procurement skills must include sourcing, close familiarity with commercial pricing models, contract terms and conditions, and negotiations. You’ll be comfortable in proactively challenging stakeholders and demand, while providing a prompt, efficient and personalised service at all levels. This is imperative, to ensure that customer needs are met, and productive relationships are built and maintained. You should also be effective in ensuring departmental policies and processes are communicated and followed. It is key that you are a self-starter with a ‘can do/will do’ attitude who has the energy, drive and commitment to make things happen and the ability to work collaboratively across teams and geographies to form alignment. The ability to identify key opportunities for Procurement support and prioritise workload effectively is essential. If you have CIPS/Project Management qualification that's great, however if you have demonstrable experience and strong performance in a similar role, we'd love to hear from you! Rewards and benefits: As you help us to shape the future, we’ve shaped our rewards and benefits to help you thrive and support your lifestyle. If successful in this role you’ll get: • A discretionary bonus based on company performance, • Private Healthcare, • SAYE (Sharesave): discretionary scheme from time to time, • Personal accident cover, • Group personal pension plan where we’ll pay up to 10%, • Holiday 25 days plus bank holidays, • Reimbursement of the cost of your annual membership of one relevant and appropriate professional body We’re committed to making a tangible impact on the climate challenge we all face. Drax is where your individual purpose can work alongside your career drive. We work as part of a team that shares a passion for doing what’s right for the future. With Drax you can shape your career and a future for generations to come. Together, we make it happen. At Drax, we’re committed to fostering an environment where everyone feels valued and respected, regardless of their role. To make this a reality, we actively work to better represent the communities we operate in, foster inclusion, and establish fair processes. Through these actions, we build the trust needed for all colleagues at Drax to contribute their perspectives and talents, no matter their background. Find out more about our approach ___. Talk to us about flexible working! How to apply: Think this role’s for you? Click the ‘Apply Now’ button to begin your Drax journey. If you want to find out more about Drax, check out our LinkedIn page to see our latest news. We understand that you may have some additional questions about the role. If you’d like to have a confidential chat to discuss the role in more detail, please email . We reserve the right to close roles early when the particular role and / or location has had sufficient applications.

Consensus is not just a care provider – we're a community of amazing people dedicated to inspiring and empowering people with learning disabilities, autism, and complex needs. If you're as passionate as we are about making a meaningful difference in the lives of others, then this may be the job for you as we seek a new service manager to lead our amazing team in Selby, North Yorkshire. We believe ... ZIPC1_UKTJ

Building a sustainable tomorrow Are you ready to be part of a groundbreaking infrastructure project that will shape the future of energy in the UK? Eastern Green Link 2 (EGL2) is a transformative 5-year initiative delivering a 525kV, 2GW high-voltage direct current (HVDC) subsea transmission cable connecting Peterhead, Scotland to Drax, England. This will be the longest HVDC cable in the UK and the ... ZIPC1_UKTJ

We’re Hiring: Regulatory Affairs Manager Location: Woodland House, North Duffield, Selby, North Yorkshire Company: GBUK Group | Medical Devices Contract: Full-time | Hybrid Are you looking for an opportunity to join a thriving, successful business whose continued growth and passion for enhancing patient care, means you can truly make a difference? Are you confident executing a regulatory strategy to the highest standard and ensuring the successful roll-out of new innovations and product changes? If you enjoy a fast-paced role in which your work directly contributes to patient safety and you are passionate about regulatory affairs, read on… an exciting opportunity awaits! About the role: • As Regulatory Affairs Manager, you will be responsible for managing the Regulatory Affairs department under the leadership of the Head of Regulatory Affairs., • Responsible for all company regulatory product registrations, certification and maintenance., • Responsible for regulatory procedures and processes, regulatory systems and departmental ways of working., • Responsible for the overall effective planning and scheduling of workload, tasks and priorities for the senior regulatory affairs associates (direct reports), regulatory affairs associates (indirect reports) and labelling coordinators (indirect reports). Key Responsibilities: • Lead the senior regulatory affairs associates (direct reports), regulatory affairs associates (indirect reports) and labelling coordinators (indirect reports), overseeing all team responsibilities and workload, effectively planning, scheduling and assigning work/projects in line with deadlines, • Perform and support with market research and regulatory strategies to achieve market registrations of current and new devices, • Ensuring compliance with all applicable regulations, standards and guidance’s, and adhering to GBUK SOPs, • Raise, review and complete actions as part of change control process., • Work cross functionally with other departments such as but not limited to R&D, Quality affairs, Clinical Affairs, Marketing, Sales, • Review and provide input as necessary into R&D, marketing and clinical documentation and processes, • Review and completion of post market surveillance documentation and activities, lead by clinical affairs, • Communication with regulatory authorities and regulatory bodies, • Change notification tracking, writing and submission to regulatory bodies, and management of such through to approvals, • Communications with regulatory bodies and involvement in RTQ writing, review and submission, to achieve conformity assessment approval, and/or maintenance of CA mark, • Overall responsibility for maintaining the regulatory team tracker and ensuring all regulatory projects are planned and scheduled appropriately. Ensuring business critical projects (MDR, IVDR) and changes (CCRs) are implemented in a timely manner and achieved on time, • Ensuring compliance of product and product packaging, labelling, including instructions for use, product literature and any associated product claims, along with UDI compliance, • Oversee regulatory project leads for new product development and compliance projects What you can bring to the role: • Degree or equivalent certification in science related, medical, or engineering discipline., • Project management and use of various databases and computer software tools, • The ability to assess all necessary and specific regulatory obligations as appropriate for the device, to ensure regulatory compliance, • Experience of regulatory body change notification and RTQ for regulatory dossiers, • Regulatory experience within the medical devices sector, • Working knowledge of the MDD, MDR, IVDD, IVDR, UK MDR, ISO 13485 and related ISO standards, • Experience in the Compilation, review, maintenance and regulatory body submission of Class I, IIa, IIb and III EU technical documentation for CE and/or UKCA marking, • Experience in the compilation, review, maintenance and submission of 510ks and of regulatory body communication, • Experience with Clinical Evaluation compilation and Risk Management implementation to applicable standards, • Experience of people management, having set departmental objectives and performed appraisals Why Join GBUK Group? You will be part of a growing, purpose-led organisation where your work directly impacts patient care and device safety. The role offers opportunities for professional development, cross-functional collaboration, and meaningful contribution to the future of GBUK’s medical device portfolio. Equality: All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.

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If you're as passionate as we are about making a meaningful difference in the lives of others, then this may be the job for you as we seek a new service manager to lead our amazing team in Selby, North Yorkshire.

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