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This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board. Company Description Cellular Origins is developing the automated factory platforms that make this possible. As Head of Supply Chain, you'll play a central role in making sure everything behind those platforms works as it should, from specialist equipment and consumables to long-term supplier partnerships. Your work will directly support the delivery of therapies that can change lives. Head of Supply Chain Full time, on-site, Melbourn, Cambridgeshire Cell therapies are changing what is possible for patients with cancer, autoimmune disease and neurological conditions. They offer hope where treatments once ran out. But turning that promise into reality for thousands of patients depends on manufacturing systems that can scale without compromising quality, safety or control. At Cellular Origins, we are developing the automated factory platforms that make this possible. As Head of Supply Chain, you'll play a central role in making sure everything behind those platforms works as it should, from specialist equipment and consumables to long-term supplier partnerships. Your work will directly support the delivery of therapies that can change lives. This is an opportunity to build something meaningful from the ground up. You'll join us as we develop our first deployments, shaping a supply chain function that grows with the business and supports our mission for the long term. Job Description About the role As our first Head of Supply Chain, you'll define and lead the strategy, organisation and execution of supply across Cellular Origins. You'll be responsible for how we source, contract, manage and scale everything needed to design, build, deploy and support our Constellation systems. This is both a strategic and hands on leadership role. You'll work closely with Engineering, Manufacturing, Quality, Field Operations and PMO, ensuring supply decisions support GMP requirements, commercial realities and customer expectations. As the company grows, you'll grow the team, the capability and the operating model alongside it. What you'll do You'll design and embed a supply chain operating model that supports the full lifecycle of our systems, from development through to customer deployment and long term service. That includes equipment, consumables, software suppliers, sub contractors and service partners. A large part of your role will be building strong, pragmatic supplier relationships. You'll lead commercial and contractual negotiations, working closely with Legal to ensure agreements are robust, balanced and appropriate for a regulated life sciences environment. You'll take clear ownership of supplier risk, continuity planning, change control and long lead items, helping the business move quickly without taking unnecessary risk. You'll also build and lead a high performing supply chain and procurement team. You'll define roles, interfaces and priorities, creating simple structures that work now and can scale over time. As we move from early deployments into broader commercial delivery, you'll evolve governance, planning, inventory and supplier performance management in a way that supports predictability without slowing us down. In the first 6 to 12 months, you'll focus on stabilising critical supply paths for upcoming deployments, strengthening supplier contracts in high impact areas, introducing lightweight planning and inventory approaches, and ensuring we can consistently provide the evidence and traceability expected by regulated customers. Qualifications About you You enjoy building capability where none existed before, then helping it mature as complexity grows. You're comfortable working in environments where not everything is defined yet, and you bring sound judgement to balancing pace, quality and risk. You'll bring significant experience leading supply chain or procurement activity in complex, regulated environments such as cell and gene therapy, biopharma manufacturing, medical devices, automation, instrumentation or closely related life sciences fields. You've built or scaled supply chain functions before, and you're comfortable moving between hands on detail and longer term design. You understand what good looks like in GMP relevant supply, from equipment configuration and consumables control to documentation, traceability and change management. You work well with Quality and Regulatory colleagues, and you appreciate how supply chain decisions affect validation, compliance and customer confidence. You're also an experienced people leader. You've built and developed teams, created clarity around ownership and expectations, and fostered collaborative ways of working. You bring a pragmatic mindset, commercial awareness and a genuine interest in how your work supports patients at the end of the chain. Additional Information Benefits Cellular Origins is based on the TTP Campus, within purpose built sustainable offices, labs and green surroundings, 10 miles south of Cambridge. Our working culture encourages entrepreneurship, shared ideas and collaboration, while providing you the freedom to do your best work. Our employee benefits include: Annual bonus 25 days holiday Employer pension contribution of 10% of salary Free lunch and all day refreshments Private medical insurance for employees and dependants Enhanced family friendly leave Life insurance worth 6x salary Electric car leasing scheme Cycle to work scheme Season ticket loan Activities and community that supports healthy activities that bring colleagues together; whether it's lunchtime squash or football, Zumba or our own rock band. Colleagues initiate new clubs and outings whenever they feel there's something missing! Local sports facilities and theatre discounts and memberships. Ready to apply? If you'd like to build a supply chain that helps advanced cell therapies reach more patients, we'd love to hear from you. Apply now to join a team focused on turning scientific potential into reliable, scalable reality. Every application will be reviewed by the hiring team and will receive a response. Videos To Watch

Join Superdrug Head Office- Make a Real Difference Every Day! Location: East Croydon Hours: 37.5 9.00 am - 5.30 pm - Hybrid working available depending on role responsibilities with 2 days working from home and 3 days in our stylish, modern and collaborative office close to East Croydon Station. Salary: Competitive Why Superdrug? Passionate about Beauty and Health? Want to be part of an innovative, trend setting retailer? Our vibrant Head Office, based by East Croydon station is a fantastic environment filled with hundreds of brilliant personalities. We're a team that puts our customers and our teams at the heart of everything we do. At Superdrug, we aim to be the best in accessible health & beauty, loved by our customers for value, choice, friendly advice, service and fun. Our success comes from our people - they make the difference. We're all about personality, we have fun, and we work hard to deliver That Superdrug feeling. Here's the exciting bit A day includes Role Purpose The Pharmacy Buyer is critical to the delivery of the healthcare strategy with a focus on maximising pharmacy and clinic income and margin through the successful management and negotiation of commercial agreements with suppliers, new product launches and execution of joint business plans. This role reports into the Senior Pharmacy Buyer for Superdrug. Typical day Key stakeholders include: Suppliers, Wholesalers, Healthcare Operations, Supply Chain, Merchandising, Finance, Marketing and Legal Working closely with the Healthcare Services team developing and delivering the commercial strategy Maximising income and margin through supplier negotiations Identifying and implementing new product or service opportunities to drive innovation Working with suppliers, wholesalers and Supply Chain to ensure strong product availability Reviewing and negotiating contracts Collaborating with the Marketing team and suppliers to agree and implement strong marketing plans Collaborating with Healthcare Operations and suppliers to deliver training and improve in store processes Working on cross functional projects across the wider Healthcare team to exceed customer needs and help deliver the Healthcare strategy Developing, building and maintaining strong internal and external relationships to support and enhance the Superdrug proposition Providing exceptional service to customers both internal and external, working to proactively resolve issues and drive efficiencies A good fit for you You thrive in a fast paced, ever changing environment You want to add value through collaborative working, and ensuring people feel engaged and involved You take pride in your attention to detail and ability to effectively plan and prioritise your workload You have strong analytical skills and enjoy analysing data You are great at building business relationships and enjoy working collaboratively with your team and your stakeholders You get satisfaction through seeing your hard work and plans come together and have real business impact You are motivated by delivering results and can easily work to deadlines You enjoy learning new systems and finding more efficient ways of working You have a proactive mindset and can understand and interpret the bigger picture You're a strong communicator who can easily help others to understand your perspective Requirements Confidence in office 365 products, in particular Microsoft Excel Knowledge of Retek, Business Objects and Power Bi is an advantage Excellent numerical, organisational and time management skills Experience working in retail or for a pharmaceutical or healthcare company would be ideal but not essential Experience in the core principles of buying - negotiation, category management, supplier relationships Benefits 33 days holiday rising to 38 days with length of service (inclusive of bank holidays) 2 staff discount codes for yourself and a family member or friend 30% discount on Superdrug Own Brand Products both in store and online Hybrid working patterns available depending on role responsibilities with 2 days working from home and 3 days in our stylish, modern and collaborative office close to East Croydon Station Company pension matching and bonus We offer Stream - a money management app that gives you access to a percentage of your pay as you earn it Being part of more! We are part of a group who work closely with Savers, The Perfume Shop and Three UK We are part of A.S. Watson Group, the world's largest international health and beauty retailer with over 15,700 stores in 25 markets! Unrivalled Learning and Development programmes Enhanced maternity/shared parental/adoption leave, company sick pay and pregnancy loss and support Come and be part of something special! For information on how we manage and store your data please go to

Overview We are seeking a dedicated and compassionate Salaried GP to join our practice team at Dean Medical Practice. We are located in the Forest of Dean, close to the Wye Valley and the Welsh Borders with good road links to Gloucester, Cheltenham, South Wales and Bristol. Working over 3 sites: Coleford Health Centre, Coleford, GL16 8RH; Brunston Surgery, Coleford, GL16 8HJ; Lydbrook Health Centre, Lydbrook, GL17 9LG. A new build is approved with an expected new build in 2027. This is an excellent opportunity to develop your career in a practice that values high-quality patient care, teamwork, and a healthy worklife balance. What we offer Competitive salary: £13,200 per session Thursdays & Fridays, 4 sessions per week - 19 hours Generous annual leave and study leave Supportive multidisciplinary team including First Contact Clinicians (FCC), Practice Nurses, RNAs, HCAs, GPAs, Phlebotomist, Clinical Pharmacists, Pharmacy Technician Practice Paramedic, FCC, undertakes the majority of home visits Forward-thinking, well-established practice SystmOne clinical system CQC-rated Good Strong links with local PCN and community services Located in the heart of the Forest of Dean offering affordable housing, excellent schools, and outstanding countryside on your doorstep Important notes The Care Quality Commission requires us to have a complete employment history from the age of 16, including explanations for any gaps in employment. Closing Date: 17th March 2026. Interview Date: 1st April 2026. Main duties of the job Primary care clinician duties, including face-to-face consultations, video consultations, telephone consultations, e-consultations and queries. Also, home visits, duty doctor/on-call responsibilities, clinical administration, prescribing, and dealing with queries, paperwork and correspondence in a timely fashion. Acting as Named GP for a share of registered patients proportionate to contracted hours. Complying with the General Medical Council's Good Medical Practice and other standards for doctors. About us G DOC LTD is a GP-owned organisation; all GP surgeries in Gloucestershire are our shareholders. We operate with a not-for-profit ethos, ensuring every decision and service focuses on improving patient outcomes and reinvesting in local Primary Care across the county. We directly manage several GP surgeries in Gloucester and the Forest of Dean, providing patient-centred care to more than 45,000 patients. We value continuity of care and pride our practice teams. In addition to our surgeries, we deliver a range of countywide commissioned services designed to improve access, increase capacity, or provide specialist support. Our teams are committed to delivering sustainable, high-quality primary care while fostering innovation and collaboration across the local health system. By joining us, you'll be part of an organisation that puts people first, supporting staff wellbeing, professional development, and a collaborative culture. You'll benefit from the stability, support, and career opportunities of a larger organisation, while still working in close-knit, community-focused teams. Job responsibilities What we're looking for A motivated and compassionate GP Committed to providing high-quality, patient-centred care Willing to work collaboratively as part of a supportive team Duties Specific to Role Surgery consultations and emergencies, telephone consultations and queries, triaging, visiting patients at home, checking and signing repeat prescriptions and dealing with queries, patient test results, patient medical reports and examinations (e.g. for insurance) on behalf of the Practice, referral letters, and NHS/private paperwork and correspondence Undertaking a share of the clinical and administrative work of the Practice, including pooled clinical admin, QOF, audits, prescribing reviews Making professional, autonomous decisions in relation to presenting problems, whether self-referred or referred from other health care workers within the organisation Recording clear and contemporaneous consultation notes to agreed standards Collecting data for audit purposes as per Practice protocols Reviewing patients for quality improvement and safety (e.g., MRHA safety alerts and long-term condition reviews) Prescribing in accordance with locally agreed or national guidelines Cover for other doctors by reciprocal sharing of correspondence, results and prescriptions for absent doctors Working conditions Frequent, prolonged VDU use Time-pressured environment High levels of accuracy and attention to detail essential at all times Exposure to distressing situations and written material Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Person Specification Experience Excellent communication skills (written and oral). Willing to become competent in use of SystmOne if not already. Ability to follow policy and procedure. Able to identify and resolve risk management issues according to policy or protocol. Effective time management. Ability to work as a team member and autonomously. Good interpersonal skills. Competent in use of SystmOne. Competent in the use of Office and Outlook. Qualifications Undergraduate degree in Medicine or GMC-recognised equivalent Current registration with General Medical Council and on GMC GP register On National Performers List MRCGP or equivalent Level 3 safeguarding training up to date or, if lapsed, willing to ensure training up to date before commencing post Other Disclosure Barring Service (DBS) enhanced check satisfactory. Evidence of continuing professional development Personal Qualities Clear, polite telephone manner. Polite and confident. Flexible and cooperative. Motivated. High levels of integrity and loyalty. Sensitive and empathetic in distressing situations. Ability to work under pressure Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

Team Secretary/Administrator (MH&LD - Psychological Therapies, SCAMHS) An exciting chance to make a real impact has opened up for a proactive, experienced, and people-focused professional to join our Administration Team as a Team Secretary/Administrator for the Specialist Child & Adolescent Mental Health Services at Ty Llewelyn, Glangwili Hospital. Experience of a range of IT systems including Microsoft Word, Excel Management, Data Collection, Power Point, and E-Mail, coupled with proven secretarial skills and previous experience is essential. Main duties of the job The post holder will be required to undertake a wide range of duties including receipt and distribution of mail, first point of contact for the service, and operate our patient administration systems, (WPAS) and Care Partner. The successful candidate will also be required to process referrals and maintain an accurate database. They will be expected to demonstrate excellent organisation skills and be flexible and adaptable in their approach to work. They must be able to work on their own initiative, use tact and diplomacy where appropriate and possess excellent communication skills. The successful candidate will be required to support the delivery of a quality comprehensive service to the team and provide cover in the event of administrative staff absences. The role may also involve travelling to and working across other sites within the Directorate in support of service delivery. In line with the Transformation of Mental Health Services, the successful candidate may be required to provide administrative support for the delivery of a 7-day service in the future. The ability to speak Welsh is desirable for this post; English and/or Welsh speakers are equally welcome to apply. About us Hywel Dda University Health Board plans and provides NHShealthcare services for people living in Carmarthenshire, Ceredigion,Pembrokeshire, and bordering counties. We have over 13,000 staff and together we provide primary,community, in-hospital, mental health and learning disabilitiesservices. We work in partnership with the three local authorities, as well aspublic, private and third sector colleagues, including our valuedteam of volunteers. Our services are provided in: Bronglais Hospital in Aberystwyth; Glangwili Hospital in Carmarthen; Prince Philip Hospital inLlanelli; and Withybush Hospital in Haverfordwest Five community hospitals: Amman Valley and Llandoveryhospitals in Carmarthenshire; Tregaron Hospital inCeredigion; and Tenby and South Pembrokeshire hospitals inPembrokeshire Two integrated care centres: Aberaeron and Cardigan inCeredigion, and several other community settings 47 general practices (six of which are health board managedpractices); dental practices (including four orthodontic); 97community pharmacies; 43 general ophthalmic practices;and 8 ophthalmic domiciliary providers Numerous mental health and learning disabilities services Job responsibilities You will be able to find a full job description and person specification attached within the supporting documents. The Health Board is committed to supporting its staff to fully embrace the need for bilingualism thereby enhancing patient and service user experiences. In our commitment to increase the number of staff who are able to communicate in Welsh with patients and professionals, we welcome applications from Welsh speakers. The ability to communicate in Welsh is desirable for this post. If you do not meet the Welsh Language requirements specified, the Health Board offers a variety of learning options and staff support to help you meet these minimal desirable requirements during the course of your employment with us. Interviews will be held on 25.03.2026 Person Specification Qualifications and knowledge ECDL / GCSE or above qualification in ICT Knowledge of Clinical / Medical Terminology Experience Experience of using Microsoft Office packages Excel, Word, PowerPoint, Access, MS Teams, Desktop Publishing and E-mail Experience of working in an administrative role within a busy office environment Experience of producing and maintaining spreadsheets & databases Experience of taking and transcribing minutes of meetings Experience of working in a multidisciplinary team Experience of patient administration systems Experience with working with TPro. Familiar and confident using e-mail and searching the internet Understanding of/ or experience of working within Mental Health and/ or Learning Disabilities Language Skills Welsh Speaker (Level 1) Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. £25,313 to £26,999 a yearper annum pro rata

Manufacturing Administrator Location: Near Yeovil Perm role £ 26,000 - 30,000 DOE My client, a well-established and successful family-owned FMCG manufacturing business, is seeking to appoint a Manufacturing Administrator / Stock and Sales Administrator for their facility located on the outskirts of Yeovil, near Wincanton. Operating from contemporary premises, the appointed Administrator will play a pivotal role within the office team, providing technical and quality support, managing stock administration for production, and assisting the accounts department with sales administration. This position is particularly suited to candidates possessing prior experience in manufacturing administration who are keen to further develop their careers. Key Responsibilities Complete, process, and file documentation related to Goods In, Goods Out, and stock control. Support comprehensive stock traceability throughout the manufacturing process. Maintain accurate records using an ERP/MRP system. Assist with client sales, technical, and quality enquiries. Manage internal stock and facilitate physical stock checks. Provide general sales and office administrative support. Skills & Experience Required Proficient in computer usage, preferably with experience in modern MRP systems, specifically Bills of Material. Previous background in manufacturing, food, beverage, pharmaceutical, or packaging industries is preferred. Strong analytical, numerical, and communication abilities. Exceptional attention to detail. Effective communication skills for regular interaction with factory personnel and customers. Excellent organisational skills, both written and verbal, essential due to the high volume of products managed. Collaborative team player, adept at multitasking and willing to be hands on. Benefits Competitive base salary (dependent on experience) 28 days holiday including bank holidays Pension scheme Modern kitchen facilities On-site parking Career development opportunities Open plan office environment Christmas shutdown Working hours Monday to Friday, 08:30-16:30 This role is commutable from Yeovil, Wincanton, Shepton mallet, Castle Cary, Martock, Somerton and may suit a candidate that has previously worked in stock control as a junior administrator, stock controller, QA Quality auditor, Technical administrator, ERP administrator, Technical assistant.

We are a Primary Care Network of 3 practices with a friendly team includingpharmacists, a First Contact Physio, social prescribing link worker, mentalhealth worker as well as our nurse, HCA, GP and reception teams. The role of the eHub Administrator is to undertake a wide range ofadministrative duties to aid in the management of all incoming onlineconsultations using eConsult, for our 3 practices. The successful candidate will have excellent IT skills along with good communication andthe ability to work under pressure. You will be able to work in a systemised, process-driven way, handling andmanaging high volumes of tasks and information. Main duties of the job The following are the core responsibilities of the eHub Administrator.On occasion there may be a requirement to carry out other tasks; this will bedependent upon factors such as workload and staffing levels. To sift, triage and manage each online consultationthrough the correct pathway to the most appropriate outcome to supportpatients effective and safe care Ensure all eConsults are reviewed and processedwithin the specified timeframe Actively call patients and where appropriatetheir family and/or carer to resolve relevant admin request and queries Redirect eConsults to relevant teams Contact patients by SMS, phone & email toupdate them on their eConsult Maintain records of all activities carried out,i.e. eConsults received, coding of outcomes and other relevant fields in theEMIS Web template Maintain and develop effective communicationacross the team Proactively engage in the development of theeHub Carry out system searches as required Other administrative tasks as required Always maintain full patient confidentiality,adhering to Information Governance guidelines Undertake and complete any relevant training asassigned and ensure all training is in date About us We are a large, diverse team and Brocklebank Practice is the largest of our three practices, with a list size of 18000 patients. We are a friendly and welcoming team. Our 3 practices serve a combined list of 30,000 patients under a single partnership. Each has its own list, dynamics, and character. We team up for peer support and education, with common back-office systems. In this way, we achieve more together than we could separately. Job responsibilities JOB PURPOSE The role of the eHub Administrator is to undertake a wide range ofadministrative duties to aid in the management of all incoming onlineconsultations using eConsult. MAIN DUTIES OF THE JOB Excellent IT skills are essential along with good communication andthe ability to work under pressure. Ability to work in a systemised, process-driven way, handling andmanaging high volumes of tasks and information. JOB DESCRIPTION The following are the core responsibilities of the eHub Administrator.On occasion there may be a requirement to carry out other tasks; this will bedependent upon factors such as workload and staffing levels. To sift, triage and manage each online consultationthrough the correct pathway to the most appropriate outcome to supportpatients effective and safe care Ensure all eConsults are reviewed and processedwithin the specified timeframe Actively call patients and where appropriatetheir family and/or carer to resolve relevant admin request and queries Redirect eConsults to relevant teams Contact patients by SMS, phone & email toupdate them on their eConsult Maintain records of all activities carried out,i.e. eConsults received, coding of outcomes and other relevant fields in theEMIS Web template Maintain and develop effective communicationacross the team Proactively engage in the development of theeHub Carry out system searches as required Other administrative tasks as required Always maintain full patient confidentiality,adhering to Information Governance guidelines Undertake and complete any relevant training asassigned and ensure all training is in date The list ofduties and responsibilities is not exhaustive and will develop based on theneeds and requirements of the PCN and its patients. Person Specification References We require details for two professional referees. At least one of these should be from your last employer. We require details of: Their name Job title A company email address, or postal address, to contact them on. We do not accept professional references under a personal email account. If you can only provide one professional reference, we will accept the second one as a personal reference. You should state this when providing your referee details. Qualifications Essential: Educated to GCSE level or equivalent Essential: At least 1 years experience working in a customer service orientated environment Excellent communication skills (written and oral) Strong IT skills including Microsoft Office Numerate and literate, able to supply reports as required Clear, polite telephone manner Multi-tasking using IT (EMIS Web), email, telephone systems whilst maintaining an excellent eye for detail Effective time-management (planning and organising) Ability to work as a team member and autonomously Good interpersonal skills Problem solving and analytical skills Ability to follow policy and procedure This requires someone with a mature outlook, with a willingness to learn Polite and confident Flexible and cooperative Motivated Forward thinker High levels of integrity Sensitive and empathetic in situations involving distressed patients Ability to work in a systemised, process driven way, handling a high volume of tasks and information Desirable: Experience working in primary care Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

Park View Group Practice is a large and innovative Practice. We have 6 GP Partners, supported by a large nursing team, pharmacy team, and non-clinical team to provide the best care possible for over 10000 patients. We are also a member of Tame Valley Primary Care Network, and the Practice is supported by care co-ordinators and health coaches. We are looking for a GP administrator to work 35 hours across Monday-Friday between the hours of 8am to 5pm. The shifts are to be confirmed with the candidate. These hours include a 20 minute paid lunch/break. Main duties of the job The successful candidate must have experience of working with the general public, have excellent communication skills, strong IT skills, have a clear, polite telephone manner. You will also need to be competent in the use of Office and Outlook and ideally our clinical system EMIS Web, however, this is not essential. You must be able to manage your time and workload effectively and have the ability to work as a team member and autonomously. You must be have the ability to follow policies and procedures. About us Park View Group Practice is based in Reddish, Stockport and our Practice boundary covers Stockport, Denton, and Tameside. Benefits to joining the Practice: Christmas and Summer party paid for by the Partners Monthly lunch 25 days annual leave + birthday off + bank holidays pro rata Annual leave increments based on length of service Job responsibilities The following are the core responsibilities of the Administrator. There may be on occasion, a requirement to carry out other tasks and this will be dependent upon factors such as workload and staffing levels. Administration Monitor and process the generic mailbox. Answer incoming phone calls, transferring calls or dealing with the callers request appropriately. Initiating contact with and responding to, requests from patients, team members, and external agencies. Photocopy documentation as required. Processing referrals/general letters including 2WW/dictations. Responding and maintaining group/personal task inboxes/email. Scanning of patient-related documentation and attaching scanned documents to patients healthcare records. Input data into the patients health records as necessary. Direct requests for information i.e SAR, insurance/solicitor letters/ DVLA forms, this may included processing the request. Manage recalls for patients with long term conditions, QOF recalls and childhood immunisations. Ensure the in-house recall system is maintained within Practice policy. To have a thorough knowledge of all relevant Practice procedures. To work in accordance with written protocols including confidentiality and data handling To have a thorough knowledge of the Practice Complaints Procedure and advise patients of the same where needed. Maintain a clean, tidy and effective working area at all times. Support clinical staff with general tasks as requested. Process of registration links within emis i.e Deductions, FP22, GP2GP links. Process of incoming Lloyd George records and process of outgoing Lloyd George records. Management of Petty Cash. In addition to the primary responsibilities, the administrator may be requested to: Partake in audit as directed by the clinical team. Complete opening and closing procedures in accordance with the duty rota. Person Specification Experience -Emis web. -Docman. -Working with excel and word. -Emis web. -Docman. -Working with excel and word. -Experience of working in general practice. Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

Overview Head of Managed Access Program Delivery, Medical Communities - purpose driven, collaborative and forward thinking. Based in the UCB office in Brussels, Belgium, part of the Medical Affairs team. About the role: You will be responsible for ensuring that people living with severe or life threatening conditions who have no satisfactory treatment alternatives can gain access to UCB medicines outside of clinical studies or commercial channels. You will drive excellence in Managed Access Program operations and support the development of Managed Access Program strategies across multiple indications. You will play a central role in enabling timely access to medicines while ensuring quality, compliance and cross functional alignment. Who you'll work with You will be working in a team that partners closely with colleagues across Medical Affairs, Supply, Regulatory, Clinical Operations, Market Access, and other internal functions to deliver Managed Access Program strategies and operations. You will collaborate with senior leaders, global and regional stakeholders, and external partners to ensure consistent, high quality program execution and continuous improvement. What you'll do Provide internal guidance to teams to effectively design and execute Access Program operational plans that support medical and business objectives. Drive implementation of Managed Access Program strategies and ensure regular updates based on emerging risks, external changes or internal priorities. Deliver flawless operational execution of Managed Access Programs, including launch, maintenance and continuous oversight across the UCB portfolio. Manage program budgets, plans, timelines and vendor partnerships to secure high quality and timely delivery. Foster strong cross functional collaboration to enable aligned program decisions and monitoring of execution. Build organizational capability by identifying training needs, supporting continuous learning and contributing to long term Managed Access Program strategy. Education, experience and skills Master's degree plus a medical or healthcare related degree (such as pharmacist or medical doctor). At least ten years' experience in pharmaceutical medicine, including significant experience in Medical Affairs in an international setting. Proven experience delivering Managed Access Program strategy, planning and operational execution. Experience in clinical operations, operationalizing medicine supply, and working in complex or evolving environments. Demonstrated ability to work with cross functional teams, influence senior stakeholders and communicate complex topics clearly. Strong analytical skills, strategic thinking, adaptability and the ability to make decisions in high pressure or ambiguous situations. Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you! About us UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science. Why work with us? At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential. At UCB, we've embraced a hybrid first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office. UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA . Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . on X, Facebook, Instagram, YouTube, LinkedIn and TikTok. Job Description AbbVie is searching for an in-house Associate General Counsel for our Patent Prosecution group, part of AbbVie's Intellectual Property, Transactions, and Innovation legal team. This position will support AbbVie's pharmaceutical products and be based in our offices in North Chicago, IL, Waltham, MA, South San Francisco, CA, or Irvine, CA with a hybrid work model (onsite 3+ days/week). Acting individually and in cross-functional teams, the Associate General Counsel will develop and implement intellectual property strategies for AbbVie's products and product candidates. Responsibilities: Maximize AbbVie's competitive position through creation and implementation of intellectual property strategies Provide legal advice and counsel to cross-functional R&D and business teams on a variety of IP-related matters Draft, file, and prosecute strategically useful patent applications worldwide both directly and through management of outside counsel Challenge and defend patents in IPR, opposition, interference, and other post-grant proceedings Conduct prior art searches, analyze third-party patent positions, and conduct due diligence to support business development activities Qualifications Requirements: JD degree from an accredited law school, state bar admission enabling in-house practice (specific state not required), and registration to practice before the USPTO 8+ years of experience practicing patent law as an attorney or patent agent at a law firm and/or life sciences company, including substantial U.S. and foreign patent prosecution Experience with India, China, and emerging markets a plus Technical background relevant for pharmaceutical patent prosecution, such as: Experience with small molecule and/or biological pharmaceutical discovery & development, and/or Technical degree in relevant field, such as molecular biology, biotechnology, biochemistry, biology, chemistry, chemical engineering, or biomedical engineering Strong legal, analytical, communication, collaboration, and people skills Demonstrated ability to manage complex projects to meet deadlines Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: What AbbVie Has to Offer Our work can-and does-have a tangible, lasting impact on millions of people. But it's not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Overview Sun Chemical, a member of the DIC Group, is a leading producer of packaging and graphic solutions, color and display technologies, functional products, electronic materials, and products for the automotive and healthcare industries. Together with DIC, Sun Chemical is continuously working to promote and develop sustainable solutions to exceed customer expectations and better the world around us. With combined annual sales of more than $8.5 billion and 22,000+ employees worldwide, the DIC Group companies support a diverse collection of global customers. Sun Chemical Corporation is a subsidiary of Sun Chemical Group Coöperatief U.A., the Netherlands, and is headquartered in Parsippany, New Jersey, U.S.A. For more information, please visit our website at or connect with us on LinkedIn or Twitter. Position Summary/Overview The role manages Product Safety master data for Color Materials products and ensuring regulatory data compliance with global and regional legislations such as GHS, CLP, and EU REACH. The position carries responsibility for Safety Data Sheets of sales products and intermediates as well as supplier Safety Data Sheets and regulatory documents to be analyzed for raw material data maintenance. As an additional responsibility, the role includes specialized knowledge in sensitive applications like food contact, toys, etc. to assess and challenge information provided by suppliers when necessary. The individual will support various departments, including Product Management, Sales, Procurement, R&D, Quality Management, Trade Control, and IT regarding regulatory requests on a global level, while also providing support during official audits by authorities. Essential Job Functions Classification and labelling of Sun Chemical Color Materials products in accordance with global and country-specific chemical legislations and industry-specific regulations Analyses and documentation of information on external raw materials provided by suppliers regarding their impact on our sales products. Maintaining product safety master data for sales products, intermediates and raw materials. Creation and validation of safety data sheets within Atrion system (based on Intelligent Authoring software by Sphera) Assessment of supplier information on sensitive applications like food contact, toys, etc. Continuous review of products and raw materials in accordance with legal requirements, voluntary commitments or business needs to identify regulatory threats that could affect marketing of products Required Education and Experience Required Qualifications Minimum of 1-3+ years of experience in a regulatory affairs role within manufacturing industry (chemistry, pharmaceutical, etc.) Bachelor's Degree in natural sciences (preferably in chemistry) Extensive specialist knowledge in the areas of chemicals legislation (REACH, GHS, CLP) and product safety Minimum of 1-3+ years of experience with SAP R/3 business software and/or Sphera Intelligent Authoring and used to work with MS Office applications (Excel, Word, etc.) Preferred Qualifications Knowledge in pigment chemistry and printing inks Benefits We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, medical, dental, vision, short and long term disability benefits, 401(k) + match and life insurance. Eligibility of benefit timing may vary. Equal Employment Opportunity It is Sun's policy that applicants for employment are recruited, selected, and hired on the basis of individual merit and ability with respect to the position being filled. Sun prohibits discrimination on the basis of race, color, religion, creed, national origin, age, gender, sexual orientation, gender identity, marital or veteran status, disability, or any other status protected by applicable law. Employment agencies are an important component of our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Sun Chemical or directly to hiring managers in any form without a signed contract on file, and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means. Additionally, any resume submitted without a contract in place will be considered property of Sun Chemical and no fees will be paid to the agency if the candidate is hired.

Oversee daily administrative functions across the business to ensure efficient operations. Maintain central records for contracts, licences, supplier documents, and company policies. Monitor and update building and HMO licences, ensuring renewals are actioned promptly. Support meeting administration - agendas, minutes, and action tracking. Coordinate office logistics and support IT and system access requirements for the team. Line manage the Coordinator - Administration & Operations and Vertus Graduate, providing direction, workload planning, and professional development support. Oversee onboarding of new starters - ensuring systems access, equipment, and induction plans are in place. Regularly review internal systems, ensuring user access levels and approval hierarchies are up to date. Support updates to organisation charts, cost centre allocations, and system permissions as staffing changes occur. Manage intern and work experience programmes, including recruitment coordination, placement logistics, and feedback collection. Proven experience in a business administration or operations management role, ideally within property, real estate, or a professional services environment. Demonstrable experience of leading and managing a team, with direct responsibility for line reports. Experience managing financial processes such as cross-charges, invoice coding, or cost centre allocations. Experience coordinating HR administration - onboarding, systems access, and staff lifecycle changes. Track record of improving or maintaining business systems and workflows (finance, HR, or compliance platforms). Experience monitoring and reporting on spend or budgets, including pre-paid or expense card management, with responsibility for budget management and forecasting. Exposure to utilities or property administration (e.g. council tax, licences, service contracts). Experience in the Build-to-Rent, residential property, or facilities management sectors. Experience supporting operational reviews (e.g. PO or portfolio reviews) and preparing management reports. Supervisory experience - managing interns, work placements, or junior administrative staff. Previous involvement in system audits, approval hierarchies, or data governance reviews. Strong administrative and organisational skills with the ability to manage multiple streams of work simultaneously. Excellent numerical and analytical skills with attention to financial accuracy and cost allocation. Confident using Excel and other data tools for reporting, reconciliation, and tracking. Working knowledge of business systems such as Yardi, Smartsheets etc. Understanding of basic HR processes (onboarding, user access, cost centre updates). Awareness of property-related administration such as HMO licences, building licences, and utility account management. Strong written and verbal communication skills, with the ability to draft clear correspondence and maintain accurate documentation. Process improvement mindset - able to spot inefficiencies and suggest practical solutions Highly organised, methodical, and reliable - able to keep on top of multiple administrative priorities. Commercially minded with a sense of accountability for cost control and value for money. Proactive and self-motivated - takes ownership of tasks and sees them through to completion. Strong interpersonal skills; confident working across different teams and levels of seniority. Discreet and professional when handling sensitive information (financial or HR-related). Flexible and adaptable, comfortable working in a fast-paced, evolving business environment. Collaborative and approachable - a natural team player who supports others and maintains positive working relationships. HEALTH SAFETY AND WELFARE RESPONSIBILITIES ENVIRONMENTAL, SOCIAL & GOVERNANCE (ESG) RESPONSIBILITIES QUALITY MANAGEMENT RESPONSIBILITIES Find opportunities to collaborate with others across the business to achieve shared goals Encourage inclusive networks and treat others with respect and fairness Use knowledge to work effectively with suppliers / contractors to meet shared goals Confident in making decisions appropriate to the role Learn from mistakes and listen to constructive feedback to improve performance Prioritise safety and actively support community, wellbeing and sustainability programmesWe recognise the importance of embracing diverse experience, skills and perspectives at all levels and operating in an inclusive working environment, in order for everyone to reach their full potential. We also recognise that it makes business sense, since being an inclusive employer leads to better business performance and higher levels of employee engagement and satisfaction. We welcome applicants with diverse backgrounds, perspectives and skills and are committed to fostering a culture whereby everyone can reach their full potential. Flexible Working At Canary Wharf Group, our employees receive a wide range of support to help improve their skills and achieve their career goals. We offer development opportunities through classroom and e-learning training, mentoring, cross department experience and on the job learning. We heavily invest in our staff attaining accreditations to develop existing and new skills, support chartered status, sponsorships and provide further educational opportunities which are job and business related. We never stand still and continually invest in developing skills and knowledge to ensure individual and company growth. Other Benefits Canary Wharf Group (CWG) is the developer of the largest urban regeneration project in Europe. CWG develops, manages and currently owns interests in approximately 9 million square feet of mixed-use space and over 1,100 Build to Rent apartments. CWG is the largest sustainable developer in the UK and also excels operationally as it purchases 100% electricity from renewable sources since 2012 and zero waste to landfill since 2009. CWG has created a 24/7 city where people can live, work and thrive on the Canary Wharf estate and enjoy all the benefits: great transport links, access to green spaces and waterside living; and a wide range of amenities including an award-winning arts and events programme. Canary Wharf's retail offering comprises over 300 shops, including grocery stores, pharmacies, health clubs, bars and restaurants, all within 15 minutes' walk. The Company's current £2bn construction activity and pipeline includes more than 500k sq ft NIA of commercial properties and over 2,300 new homes for sale and rent.