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Job Title :CT Radiographer Banding:Band 7 Locat io n:Worthing , West Sussex Start date:ASAP Duration:Ongoing Rate :£ 3 0 - £3 1 per hour Working hours:3 long days per week An excellent opportunity is available for a Band 7 CT Radiographer to join a dedicated imaging team in Worthing. This position is ideal for a radiographer with strong CT experience who is confident working independently and committed to delivering high-quality diagnostic services. The successful candidate will play a key role in supporting the care and diagnosis of the client’s patients in a busy and well-equipped department. The CT Radiographer will be responsible for performing a variety of CT examinations with precision and care, ensuring optimal image quality and patient safety. Duties include preparing and positioning patients, operating CT equipment in line with clinical protocols, and maintaining accurate records. The role requires effective communication with patients and colleagues, a commitment to high standards of care, and adherence to all safety and quality assurance procedures. Flexibility to work long shifts is essential to meet service demands. • HCPC registration as a Diagnostic Radiographer, • Significant experience in CT imaging, ideally at Band 7 level, • Strong understanding of CT protocols and radiation safety, • Excellent patient care and communication skills, • Ability to work independently and collaboratively within a team, • Flexible approach to working long shifts If you consider yourself to have a disability or require any reasonable adjustment during the recruitment process or within the workplace, please highlight this at the earliest opportunity by contacting our team. With this information, we will provide appropriate support to you throughout the process and into your work placement. We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List. #J-18808-Ljbffr

Worthing Band 7 Locum MRI Radiographer Band: 7 Location: Worthing Start Date: ASAP Pay Rate: £30.00 - £231.00 Shift: 3x 12-hour shifts (08:00 - 20:00), Monday to Sunday About the role: An exciting opportunity has arisen for an experienced Band 7 Locum MRI Radiographer to join a leading healthcare team in Worthing. This role offers flexible shift patterns, working three 12-hour shifts per week, including weekdays and weekends. The ideal candidate will have strong MRI scanning experience, be confident in working independently, and uphold the highest patient care and imaging standards. Responsibilities: As an MRI Radiographer, you will be responsible for performing high-quality MRI scans, ensuring the safety and comfort of patients throughout the imaging process. You will work closely with radiologists and other healthcare professionals to support accurate diagnosis and patient care. Key duties include positioning patients correctly, adjusting scanning parameters as needed, operating MRI equipment efficiently, and maintaining accurate imaging records. You will also be responsible for ensuring compliance with safety protocols, troubleshooting technical issues, and contributing to the overall efficiency of the imaging department. Requirements: • BSc in Diagnostic Radiography or equivalent qualification., • HCPC registration (Health and Care Professions Council)., • Extensive MRI scanning experience, preferably at a senior level., • Proficiency in using Siemens, Philips, or GE MRI scanners (preferred but not essential)., • Strong knowledge of MRI safety protocols and best practices., • Excellent communication and patient care skills., • Ability to work independently and within a multidisciplinary team. Why work with Pulse? From the moment you register with us, our focus is entirely on you. During our first conversation, you'll quickly see that we understand your specialty inside and out. Our expert recruitment consultants are dedicated to finding you the best opportunities and supporting you every step of the way to secure the perfect placement. With our preferred or sole supplier status with many clients, you'll have access to exclusive opportunities that you won't find anywhere else. We always prioritize your best interests, engaging in meaningful conversations and truly listening to you. You are an individual, a professional-not just a resource. Reasonable Adjustments: If you consider yourself to have a disability or require any reasonable adjustment during the recruitment process or within the workplace, please highlight this at the earliest opportunity by contacting our team. With this information, we will provide appropriate support to you throughout the process and into your work placement. We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List. #J-18808-Ljbffr

Sussex Partnership NHS Foundation Trust in Worthing invites applications for a full-time Band 7 Professional Nurse Educator (PNE) in dementia inpatient care. The post collaborates with the Matron and Senior Nursing Leadership to advance governance, quality, standards, education and clinical practice. The PNE will develop and evaluate education programmes, ensure high-quality placements, support learners including student nurses and international nurses, and travel as required in discussion with #J-18808-Ljbffr

The Executive Assistant is responsible for providing high-level administrative support to the Chief Marketing Officer, in achieving their objectives and responsibilities as well as supporting the marketing team. Reporting directly to the CMO, the Marketing EA supports the CMO and his wider senior management teams; organises and coordinates executive outreach and external relations efforts whilst also organizing special events for the company as required. • Provide high-level executive and administrative support to the CMO, ensuring commitments, priorities and responsibilities are delivered effectively and on time., • Manage complex diaries, emails, communications and forward planning across multiple time zones., • Coordinate internal and external meetings, and customer engagements; prepare agendas, presentations, • Arrange international travel, accommodation, visas, transfers and itineraries for the CMO, • Plan and coordinate special events, including budgeting, venue and supplier management., • Manage relationships with travel agent, transport providers and hotels, including account set-up and ongoing administration., • Provision of administrative services to the marketing team, • Coordination of marketing meetings, online and in person, • Procurement and management of print and promotional items, and prepare for shipment as required., • Support with the purchasing administration for the marketing department through raising of purchase orders and payment of invoices, liaison with suppliers and the finance team to reconcile payments., • Prepare and process expenses, ensuring compliance with company policy and timely submission/payment., • Support onboarding of news starters to the Marketing team, • Proactively identify priorities, anticipate requirements and maintain a high level of accuracy and confidentiality., • Work collaboratively with other EAs to provide effective cover during periods of absence., • Undertake other duties reasonably required of an Executive Assistant., • Demonstrable experience of supporting senior-level executives, preferably in an international environment, handling confidential and sensitive information with the utmost discretion, • Advanced Proficiency in Microsoft Office (Outlook, Word, Excel, and PowerPoint), • Ability to communicate effectively and professionally, • Demonstrates excellent time management capabilities and ability to manage multiple calendars, • Highly organised and a great communicator Must be confidential and a team player, • Able to work with Microsoft Word, Excel and PowerPoint, • Comfortable working within a MS Teams environment, • On-site Restaurant for affordable, convenient meals, • Private Healthcare (access to remote GP & Counselling) for peace of mind, • Monthly Massages to relax and recharge, • On-site Parking for convenience and cost efficiency, • Annual Wellbeing Reimbursement to care for your mind and body, • Pension Plan to secure your future, • Cycle-to-work Scheme to stay active and eco-friendly, • Enhanced Parental Pay to support new families, • Referral Bonus to benefit from recommending talent #J-18808-Ljbffr

Worthing Job Title:Orthopaedic Specialist Physiotherapist Banding:Band 6 Location:Worthing Start:ASAP Duration:Ongoing Rate:£25 - £26 per hour Working Hours:Full-time We are seeking an exceptionally skilled and motivated Orthopaedic Specialist Physiotherapist to join our esteemed client in Worthing. This role requires working in a fast-paced and dynamic healthcare environment, where you will be responsible for providing specialised physiotherapy care for orthopaedic patients. Your advanced expertise will be pivotal in ensuring the precision and reliability of patient care, which is critical for accurate diagnosis and treatment. Key Responsibilities: In this role, you will be responsible for assessing and managing orthopaedic patients, developing and implementing tailored physiotherapy plans, and monitoring patient progress. You will work closely with the multidisciplinary team (MDT) to ensure comprehensive patient care, provide education and support to patients and their families, and maintain meticulous records and documentation. Qualifications and Experience: • HCPC registration., • Bachelor’s degree in Physiotherapy or a related field., • Extensive experience in orthopaedic physiotherapy., • Exceptional analytical and problem-solving abilities., • Unwavering attention to detail and accuracy., • Proven ability to work both independently and collaboratively within a team. Why Work with Pulse? From the moment you register with us, our focus is entirely on you. During our first conversation, you’ll quickly see that we understand your specialty inside and out. Our expert recruitment consultants are dedicated to finding you the best opportunities and supporting you every step of the way to secure the perfect placement. With our preferred or sole supplier status with many clients, you’ll have access to exclusive opportunities that you won’t find anywhere else. We always prioritise your best interests, engaging in meaningful conversations and truly listening to you. You are an individual, a professional—not just a resource. Reasonable Adjustments: If you consider yourself to have a disability or require any reasonable adjustment during the recruitment process or within the workplace, please highlight this at the earliest opportunity by contacting our team. With this information, we will provide appropriate support to you throughout the process and into your work placement. We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of Practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List. #J-18808-Ljbffr

Worthing Job Title:Respiratory Physiotherapist (Acute Medicine and Admissions) Banding:Band 6 Location: Worthing Start:ASAP Duration:Ongoing Rate:£25 - £26 per hour Working Hours:Full-time We are seeking an exceptionally skilled and motivated Respiratory Physiotherapist who specialises in acute medicine and admissions to join our esteemed client in Worthing. This role requires working in a fast-paced and dynamic healthcare environment, where you will be responsible for providing specialised respiratory care and managing patients in acute medicine and admissions. Your advanced expertise will be pivotal in ensuring the precision and reliability of patient care, which is critical for accurate diagnosis and treatment. In this role, you will be responsible for assessing and managing patients in acute medicine, admissions, and respiratory care. You will develop and implement tailored respiratory therapy plans, monitor patient progress, and work closely with the multidisciplinary team (MDT) to ensure comprehensive patient care. You will also provide education and support to patients and their families, and maintain meticulous records and documentation. • HCPC registration., • Bachelor’s degree in Physiotherapy or a related field., • Extensive experience in acute medicine, admissions, and respiratory care., • Exceptional analytical and problem-solving abilities., • Unwavering attention to detail and accuracy., • Proven ability to work both independently and collaboratively within a team. If you consider yourself to have a disability or require any reasonable adjustment during the recruitment process or within the workplace, please highlight this at the earliest opportunity by contacting our team. With this information, we will provide appropriate support to you throughout the process and into your work placement. We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of Practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List. #J-18808-Ljbffr

Job Title:Urology Sonographer Banding:Band 7 Location:Worthing, West Sussex Start:ASAP Duration:4 months Rate:£30 - £31 per hour Working Hours:08:30 - 16:30 We are seeking an exceptionally skilled and motivated Urology Sonographer to join our esteemed client in Worthing. This role requires working in a fast-paced and dynamic environment, where you will be responsible for providing high-quality urology sonography services to patients. Your advanced expertise will be pivotal in ensuring the precision and reliability of patient care and treatment. In this role, you will be responsible for conducting a broad spectrum of urology sonography tests, maintaining, calibrating, and troubleshooting sonography equipment, and ensuring strict adherence to all relevant health and safety regulations. You will analyse and interpret complex test results with a high degree of accuracy, maintain meticulous records and documentation, and collaborate effectively with multidisciplinary healthcare teams to deliver superior patient care. • HCPC registration., • Bachelor’s degree in Sonography or a related field., • Extensive experience in urology sonography., • Exceptional analytical and problem-solving abilities., • Unwavering attention to detail and accuracy., • Proven ability to work both independently and collaboratively within a team. If you consider yourself to have a disability or require any reasonable adjustment during the recruitment process or within the workplace, please highlight this at the earliest opportunity by contacting our team. With this information, we will provide appropriate support to you throughout the process and into your work placement. We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of Practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List. #J-18808-Ljbffr

Worthing, Sussex Job Title: CAMHS Psychiatry Grade: Consultant Location: Worthing, Sussex Working Hours:40 hours Rate: Competitive, to be discussed upon application As a Consultant in Child and Adolescent Psychiatry in the UK, your responsibilities are both broad and specialised. You are primarily responsible for providing expert clinical assessments and diagnoses for children and adolescents experiencing complex mental health issues. This involves leading and overseeing the development of comprehensive treatment plans and therapeutic interventions. You are expected to manage and support multidisciplinary teams, ensuring effective collaboration between various healthcare professionals, including psychologists, social workers, and nurses. In addition, you play a key role in supervising and mentoring junior staff and trainees, contributing to their professional development. You also engage in regular MDT (Multidisciplinary Team) meetings to discuss patient progress, share insights, and adjust treatment strategies as necessary. Furthermore, you may be involved in service development and quality improvement initiatives, aiming to enhance the overall effectiveness and efficiency of CAMHS services. • You must have a full GMC licence to practice, • Previous experience in CAMHS, • Section 12, • Approved clinician status is desired but not essential If you consider yourself to have a disability or require any reasonable adjustment during the recruitment process or within the workplace, please highlight this at the earliest opportunity by contacting our team. With this information, we will provide appropriate support to you throughout the process and into your work placement. We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List. #J-18808-Ljbffr

We are looking for an analytical and detail-oriented engineer or technical specialist who enjoys understanding how products can fail, identifying risks, and working with multidisciplinary teams to develop practical solutions. Whilst experience with medical device risk management is advantageous, we are equally interested in candidates who can demonstrate strong problem-solving skills, technical curiosity, systems thinking and the ability to work with complex information. We recognise that excellent risk management professionals can come from a variety of technical backgrounds. Full training and mentoring will be provided on Rayner's Risk Management processes, tools and the practical application of ISO 14971. Please note that this role is based on-site at Global HQ in Worthing, West Sussex. • Lead the development and maintenance of Product Risk Management documentation for new and existing medical devices, working within established company procedures and international standards. Training will be provided on the specific application of ISO 14971 where required., • Facilitate cross-functional risk reviews, ensuring appropriate input is obtained from engineering, manufacturing, quality, clinical and regulatory stakeholders., • Capture and document risk assessments relating to product design, manufacturing processes and product use, ensuring information is accurate, traceable and maintained in accordance with company procedures, • As part of the R&D Product Risk Management team, represent the R&D Product Risk Management function on multi-disciplinary teams working on research, NPD, process improvement, regulatory and clinical projects, providing information, guidance and support on all product risk management aspects., • Work closely with R&D, Vigilance, Quality, Validation, Process Engineering, Production and external suppliers (factored products only) to effectively and efficiently maintain Product Risk Management files in accordance with company SOPs and international standards., • Ensure that Risk Control Measures (e.g. Manufacturing SOPs, Design Verification and Biological Evaluation activities) are appropriate and up to date as company processes and practices continuously improve., • Maintain a high standard of professional and technical knowledge by attending educational training/workshops, reviewing professional publications, establishing networks, and participating in professional societies., • Broad technical awareness and the ability to understand engineering concepts across product design, manufacturing and software-controlled systems., • Competence in key Microsoft Office packages (including Outlook, Word, Excel, Teams, SharePoint), • Strong analytical and problem-solving skills, including the ability to identify trends, draw logical conclusions and challenge assumptions., • Demonstrable experience of effectively processing large amounts of data and Information In a methodical manner within a highly structured environment, • Proven ability to generate high-quality Technical Documentation, • Knowledge of medical device regulations and standards., • Familiarity with ISO 14971, ISO 13485 or Design Control processes., • Experience with risk assessment methodologies such as FMEA, Fault Tree Analysis (FTA), Hazard Analysis or similar techniques., • Experience working in a regulated or highly controlled environment (e.g. medical devices, pharmaceuticals, aerospace, automotive, defence or other safety-critical industries)., • Qualification in Engineering or relevant technical discipline, • On-site Restaurant for affordable, convenient meals, • Private Healthcare (access to remote GP & Counselling) for peace of mind, • Monthly Massages to relax and recharge, • On-site Parking for convenience and cost efficiency, • Annual Wellbeing Reimbursement to care for your mind and body, • Pension Plan to secure your future, • Cycle-to-work Scheme to stay active and eco-friendly, • Enhanced Parental Pay to support new families, • Referral Bonus to benefit from recommending talent #J-18808-Ljbffr

We are looking for an analytical and detail-oriented engineer or technical specialist who enjoys understanding how products can fail, identifying risks, and working with multidisciplinary teams to develop practical solutions. Whilst experience with medical device risk management is advantageous, we are equally interested in candidates who can demonstrate strong problem-solving skills, technical curiosity, systems thinking and the ability to work with complex information. We recognise that excellent risk management professionals can come from a variety of technical backgrounds. Full training and mentoring will be provided on Rayner's Risk Management processes, tools and the practical application of ISO 14971. Please note that this role is based on-site at Global HQ in Worthing, West Sussex. • Lead the development and maintenance of Product Risk Management documentation for new and existing medical devices, working within established company procedures and international standards. Training will be provided on the specific application of ISO 14971 where required., • Facilitate cross-functional risk reviews, ensuring appropriate input is obtained from engineering, manufacturing, quality, clinical and regulatory stakeholders., • Capture and document risk assessments relating to product design, manufacturing processes and product use, ensuring information is accurate, traceable and maintained in accordance with company procedures, • As part of the R&D Product Risk Management team, represent the R&D Product Risk Management function on multi-disciplinary teams working on research, NPD, process improvement, regulatory and clinical projects, providing information, guidance and support on all product risk management aspects., • Work closely with R&D, Vigilance, Quality, Validation, Process Engineering, Production and external suppliers (factored products only) to effectively and efficiently maintain Product Risk Management files in accordance with company SOPs and international standards., • Ensure that Risk Control Measures (e.g. Manufacturing SOPs, Design Verification and Biological Evaluation activities) are appropriate and up to date as company processes and practices continuously improve., • Maintain a high standard of professional and technical knowledge by attending educational training/workshops, reviewing professional publications, establishing networks, and participating in professional societies., • Broad technical awareness and the ability to understand engineering concepts across product design, manufacturing and software-controlled systems., • Competence in key Microsoft Office packages (including Outlook, Word, Excel, Teams, SharePoint), • Strong analytical and problem-solving skills, including the ability to identify trends, draw logical conclusions and challenge assumptions., • Demonstrable experience of effectively processing large amounts of data and Information In a methodical manner within a highly structured environment, • Proven ability to generate high-quality Technical Documentation, • Knowledge of medical device regulations and standards., • Familiarity with ISO 14971, ISO 13485 or Design Control processes., • Experience with risk assessment methodologies such as FMEA, Fault Tree Analysis (FTA), Hazard Analysis or similar techniques., • Experience working in a regulated or highly controlled environment (e.g. medical devices, pharmaceuticals, aerospace, automotive, defence or other safety-critical industries)., • Qualification in Engineering or relevant technical discipline, • On-site Restaurant for affordable, convenient meals, • Private Healthcare (access to remote GP & Counselling) for peace of mind, • Monthly Massages to relax and recharge, • On-site Parking for convenience and cost efficiency, • Annual Wellbeing Reimbursement to care for your mind and body, • Pension Plan to secure your future, • Cycle-to-work Scheme to stay active and eco-friendly, • Enhanced Parental Pay to support new families, • Referral Bonus to benefit from recommending talent #J-18808-Ljbffr

Worthing Band 6 Locum General Radiographer Location: Worthing Start Date: ASAP Duration: Ongoing Working Hours: Monday to Friday 0900-1700 Pay Rate: £25.00 - £26.00 We are seeking a Band 6 Locum General Radiographer to join a well-established radiology department in Worthing. This is a fantastic opportunity for a skilled radiographer to contribute to a dynamic and supportive team, providing high-quality imaging services. The successful candidate will be responsible for delivering efficient and accurate diagnostic imaging, ensuring patient safety and comfort at all times. Key Responsibilities: As a General Radiographer, you will be responsible for performing a range of diagnostic radiographic procedures, including X-rays and general imaging in a hospital setting. You will work closely with radiologists, consultants, and other healthcare professionals to provide high-quality images that aid in patient diagnosis and treatment. The role requires a strong focus on patient care, quality assurance, and radiation safety protocols. Additionally, you will assist in maintaining imaging equipment and ensuring compliance with clinical governance and departmental policies. Requirements: • BSc in Diagnostic Radiography or equivalent., • Previous NHS or private sector experience as a General Radiographer., • Proficiency in general X-ray and trauma imaging., • Strong understanding of radiation protection guidelines and safety procedures., • Excellent communication and teamwork skills., • Ability to work efficiently in a fast-paced clinical environment. Why work with Pulse? From the moment you register with us, our focus is entirely on you. During our first conversation, you’ll quickly see that we understand your specialty inside and out. Our expert recruitment consultants are dedicated to finding you the best opportunities and supporting you every step of the way to secure the perfect placement. With our preferred or sole supplier status with many clients, you’ll have access to exclusive opportunities that you won’t find anywhere else. We always prioritize your best interests, engaging in meaningful conversations and truly listening to you. You are an individual, a professional—not just a resource. Reasonable Adjustments: If you consider yourself to have a disability or require any reasonable adjustment during the recruitment process or within the workplace, please highlight this at the earliest opportunity by contacting our team. With this information, we will provide appropriate support to you throughout the process and into your work placement. We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List. #J-18808-Ljbffr

The Executive Assistant is responsible for providing high-level administrative support to the Chief Commercial Officer, Vice President Europe, and Vice President International in achieving their objectives and responsibilities as well as ad-hoc support to their respective teams. Reporting directly to the CCO, the EA supports the CCO and his wider senior management teams; organises and coordinates executive outreach and external relations efforts whilst also organizing special events for the company as required. • Provide high-level executive and administrative support to the CCO, VP Europe and VP International, ensuring commitments, priorities and responsibilities are delivered effectively and on time., • Manage complex diaries, emails, communications and forward planning across multiple time zones and international markets., • Coordinate internal and external meetings, and customer engagements; prepare agendas, presentations, minutes and action points., • Arrange international travel, accommodation, visas, transfers and itineraries for executives, team members and visitors., • Plan and coordinate special events, including budgeting, venue and supplier management., • Manage relationships with travel agents, transport providers and hotels, including account set-up and ongoing administration., • Prepare and process expenses, invoices and purchase orders, ensuring compliance with company policy and timely submission/payment., • Provide general administrative support, including drafting correspondence, reports, presentations, proposals and internal communications., • Work collaboratively with other EAs to provide effective cover during periods of absence., • Proactively identify priorities, anticipate requirements and maintain a high level of accuracy and confidentiality., • Analyse the Salesforce opportunity pipeline, using Tableau where appropriate, to identify stalled or at-risk deals, pipeline gaps and potential revenue risks., • Assess forecast performance and pipeline-to-quota coverage, providing the CCO with data-driven recommendations, remediation plans and resource reallocation opportunities., • Support with the purchasing administration for the commercial department through raising of purchase orders and payment of invoices, liaison with suppliers and the finance team to reconcile payments., • Welcome customers when visiting HQ and provide site tours and information, organise welcome packs and merchandise to ensure a professional and friendly experience when visiting Rayner., • Undertake other duties reasonably required of a senior Executive Assistant., • Demonstrable experience of supporting senior-level executives, preferably in an international environment, handling confidential and sensitive information with the utmost discretion, • Advanced Proficiency in Microsoft Office (Outlook, Word, Excel, and PowerPoint), • Ability to communicate effectively and professionally, • Demonstrates excellent time management capabilities and ability to manage multiple calendars, • Highly organised and a great communicator, • Must be confidential and a team player, • Bachelor's degree, • Experience of working in PE, Banking, Medical/Pharma, professional services, • Competitive Salary, • On-site Restaurant for affordable, convenient meals, • Private Healthcare (access to remote GP & Counselling) for peace of mind, • Monthly Massages to relax and recharge, • On-site Parking for convenience and cost efficiency, • Annual Wellbeing Reimbursement to care for your mind and body, • Pension Plan to secure your future, • Cycle-to-work Scheme to stay active and eco-friendly, • Enhanced Parental Pay to support new families, • Referral Bonus to benefit from recommending talent #J-18808-Ljbffr

The Executive Assistant is responsible for providing high-level administrative support to the Chief Commercial Officer, Vice President Europe, and Vice President International in achieving their objectives and responsibilities as well as ad-hoc support to their respective teams. Reporting directly to the CCO, the EA supports the CCO and his wider senior management teams; organises and coordinates executive outreach and external relations efforts whilst also organizing special events for the company as required. • Provide high-level executive and administrative support to the CCO, VP Europe and VP International, ensuring commitments, priorities and responsibilities are delivered effectively and on time., • Manage complex diaries, emails, communications and forward planning across multiple time zones and international markets., • Coordinate internal and external meetings, and customer engagements; prepare agendas, presentations, minutes and action points., • Arrange international travel, accommodation, visas, transfers and itineraries for executives, team members and visitors., • Plan and coordinate special events, including budgeting, venue and supplier management., • Manage relationships with travel agents, transport providers and hotels, including account set-up and ongoing administration., • Prepare and process expenses, invoices and purchase orders, ensuring compliance with company policy and timely submission/payment., • Provide general administrative support, including drafting correspondence, reports, presentations, proposals and internal communications., • Work collaboratively with other EAs to provide effective cover during periods of absence., • Proactively identify priorities, anticipate requirements and maintain a high level of accuracy and confidentiality., • Analyse the Salesforce opportunity pipeline, using Tableau where appropriate, to identify stalled or at-risk deals, pipeline gaps and potential revenue risks., • Assess forecast performance and pipeline-to-quota coverage, providing the CCO with data-driven recommendations, remediation plans and resource reallocation opportunities., • Support with the purchasing administration for the commercial department through raising of purchase orders and payment of invoices, liaison with suppliers and the finance team to reconcile payments., • Welcome customers when visiting HQ and provide site tours and information, organise welcome packs and merchandise to ensure a professional and friendly experience when visiting Rayner., • Undertake other duties reasonably required of a senior Executive Assistant., • Demonstrable experience of supporting senior-level executives, preferably in an international environment, handling confidential and sensitive information with the utmost discretion, • Advanced Proficiency in Microsoft Office (Outlook, Word, Excel, and PowerPoint), • Ability to communicate effectively and professionally, • Demonstrates excellent time management capabilities and ability to manage multiple calendars, • Highly organised and a great communicator, • Must be confidential and a team player, • Bachelor's degree, • Experience of working in PE, Banking, Medical/Pharma, professional services, • Competitive Salary, • On-site Restaurant for affordable, convenient meals, • Private Healthcare (access to remote GP & Counselling) for peace of mind, • Monthly Massages to relax and recharge, • On-site Parking for convenience and cost efficiency, • Annual Wellbeing Reimbursement to care for your mind and body, • Pension Plan to secure your future, • Cycle-to-work Scheme to stay active and eco-friendly, • Enhanced Parental Pay to support new families, • Referral Bonus to benefit from recommending talent #J-18808-Ljbffr

The Senior Mechanical Development Engineer is responsible for the technical leadership, development, and lifecycle management of a portfolio of ophthalmic surgical products, including phacoemulsification (Phaco) accessories and vitreoretinal (VR) instruments. Leads on technical engagement with new and existing suppliers, establishing robust design history documentation, and drives verification activities through to successful product release within a regulated medical device environment. Works in multidisciplinary project teams from across the company as well as collaborating externally with surgeons, inventors, research groups and universities. Please note that this role is based on-site at Global HQ in Worthing, West Sussex. • Acts as the technical lead and subject matter expert for the Phaco accessory and VR instrument portfolio, providing ownership throughout the product lifecycle from new product development to sustaining engineering., • Leads the mechanical design and development of new products, technologies, and product enhancements from concept through design transfer and commercial release., • Takes ownership of product performance, manufacturability, reliability, and ongoing design improvements., • Supports product lifecycle management activities, including design changes, obsolescence management, supplier changes, and continuous improvement projects., • Provides technical leadership for cross-functional project teams., • Delivers and reports on work packages within the scope of established Design Control procedures., • Creates and maintains Design History Files (DHFs) in accordance with company procedures and applicable medical device regulations., • Defines verification strategies and acceptance criteria. Develops verification protocols and test methods for Phaco accessories and VR instruments. Analyses test results and determines compliance against design requirements., • Maintains a high standard of professional and technical knowledge by attending educational training/workshops, reviewing professional publications, establishing networks, and participating in professional societies., • Degree in Mechanical Engineering, Product Design Engineering, Biomedical Engineering, or a related discipline., • Strong understanding of design control and medical device development processes., • Experience creating and maintaining Design History Files (DHFs)., • Experience leading engineering projects involving supplier qualification or manufacturing transfer., • Demonstrated experience planning and executing product verification testing., • Strong experience producing engineering documentation and technical reports., • Proficiency in CAD and engineering drawing standards., • Hands-on approach to problem-solving, root cause analysis, and technical decision-making., • Excellent stakeholder management and communication abilities., • Experienced in design and development of ophthalmic surgical devices, phacoemulsification systems, surgical instruments or disposable medical devices, sterile barrier packaging., • Experienced in high precision metal component design, CNC machining, and testing., • Experienced in small plastic component design, injection moulding, vacuum form moulding and testing., • Experience of working with international suppliers and contract manufacturers., • Understanding of process validation, and process qualification activities., • Familiarity with relevant medical device standards including ISO 13485 (Design Control section), ISO60601-1 and -2, ISO 80601-2-58, ISO 62366, and applicable packaging and transport standards., • On-site Restaurant for affordable, convenient meals, • Private Healthcare (access to remote GP & Counselling) for peace of mind, • Monthly Massages to relax and recharge, • On-site Parking for convenience and cost efficiency, • Annual Wellbeing Reimbursement to care for your mind and body, • Pension Plan to secure your future, • Cycle-to-work Scheme to stay active and eco-friendly, • Enhanced Parental Pay to support new families, • Referral Bonus to benefit from recommending talent #J-18808-Ljbffr

The Senior Mechanical Development Engineer is responsible for the technical leadership, development, and lifecycle management of a portfolio of ophthalmic surgical products, including phacoemulsification (Phaco) accessories and vitreoretinal (VR) instruments. Leads on technical engagement with new and existing suppliers, establishing robust design history documentation, and drives verification activities through to successful product release within a regulated medical device environment. Works in multidisciplinary project teams from across the company as well as collaborating externally with surgeons, inventors, research groups and universities. Please note that this role is based on-site at Global HQ in Worthing, West Sussex. • Acts as the technical lead and subject matter expert for the Phaco accessory and VR instrument portfolio, providing ownership throughout the product lifecycle from new product development to sustaining engineering., • Leads the mechanical design and development of new products, technologies, and product enhancements from concept through design transfer and commercial release., • Takes ownership of product performance, manufacturability, reliability, and ongoing design improvements., • Supports product lifecycle management activities, including design changes, obsolescence management, supplier changes, and continuous improvement projects., • Provides technical leadership for cross-functional project teams., • Delivers and reports on work packages within the scope of established Design Control procedures., • Creates and maintains Design History Files (DHFs) in accordance with company procedures and applicable medical device regulations., • Defines verification strategies and acceptance criteria. Develops verification protocols and test methods for Phaco accessories and VR instruments. Analyses test results and determines compliance against design requirements., • Maintains a high standard of professional and technical knowledge by attending educational training/workshops, reviewing professional publications, establishing networks, and participating in professional societies., • Degree in Mechanical Engineering, Product Design Engineering, Biomedical Engineering, or a related discipline., • Significant experience developing or sustaining regulated medical devices., • Strong understanding of design control and medical device development processes., • Experience creating and maintaining Design History Files (DHFs)., • Experience leading engineering projects involving supplier qualification or manufacturing transfer., • Demonstrated experience planning and executing product verification testing., • Strong experience producing engineering documentation and technical reports., • Proficiency in CAD and engineering drawing standards., • Hands‑on approach to problem‑solving, root cause analysis, and technical decision‑making., • Excellent stakeholder management and communication abilities., • Experienced in design and development of ophthalmic surgical devices, phacoemulsification systems, surgical instruments or disposable medical devices, sterile barrier packaging., • Experienced in high precision metal component design, CNC machining, and testing., • Experienced in small plastic component design, injection moulding, vacuum form moulding and testing., • Experience of working with international suppliers and contract manufacturers., • Understanding of process validation, and process qualification activities., • Familiarity with relevant medical device standards including ISO 13485 (Design Control section), ISO60601-1 and -2, ISO 80601-2-58, ISO 62366, and applicable packaging and transport standards., • On‑site Restaurant for affordable, convenient meals, • Private Healthcare (access to remote GP & Counselling) for peace of mind, • Monthly Massages to relax and recharge, • On‑site Parking for convenience and cost efficiency, • Annual Wellbeing Reimbursement to care for your mind and body, • Pension Plan to secure your future, • Cycle‑to‑work Scheme to stay active and eco‑friendly, • Enhanced Parental Pay to support new families, • Referral Bonus to benefit from recommending talent #J-18808-Ljbffr

The Executive Assistant is responsible for providing high-level administrative support to the Chief Marketing Officer, in achieving their objectives and responsibilities as well as supporting the marketing team. Reporting directly to the CMO, the Marketing EA supports the CMO and his wider senior management teams; organises and coordinates executive outreach and external relations efforts whilst also organizing special events for the company as required. What You'll Be Doing: Provide high-level executive and administrative support to the CMO, ensuring commitments, priorities and responsibilities are delivered effectively and on time. Manage complex diaries, emails, communications and forward planning across multiple time zones. Coordinate internal and external meetings, and customer engagements; prepare agendas, presentations Arrange international travel, accommodation, visas, transfers and itineraries for the CMO Plan and coordinate special events, including budgeting, venue and supplier management. Manage relationships with travel agent, transport providers and hotels, including account set-up and ongoing administration. Provision of administrative services to the marketing team Coordination of marketing meetings, online and in person Procurement and management of print and promotional items, and prepare for shipment as required. Support with the purchasing administration for the marketing department through raising of purchase orders and payment of invoices, liaison with suppliers and the finance team to reconcile payments. Prepare and process expenses, ensuring compliance with company policy and timely submission/payment. Support onboarding of news starters to the Marketing team Proactively identify priorities, anticipate requirements and maintain a high level of accuracy and confidentiality. Work collaboratively with other EAs to provide effective cover during periods of absence. Undertake other duties reasonably required of an Executive Assistant. What Experience & Skills You Will Need: Essential • Demonstrable experience of supporting senior-level executives, preferably in an international environment, handling confidential and sensitive information with the utmost discretion, • Advanced Proficiency in Microsoft Office (Outlook, Word, Excel, and PowerPoint), • Ability to communicate effectively and professionally, • Demonstrates excellent time management capabilities and ability to manage multiple calendars, • Highly organised and a great communicator Must be confidential and a team player Desirable • Able to work with Microsoft Word, Excel and PowerPoint, • Comfortable working within a MS Teams environment What We Can Offer You: • On-site Restaurant for affordable, convenient meals, • Private Healthcare (access to remote GP & Counselling) for peace of mind, • Monthly Massages to relax and recharge, • On-site Parking for convenience and cost efficiency, • Annual Wellbeing Reimbursement to care for your mind and body, • Pension Plan to secure your future, • Cycle-to-work Scheme to stay active and eco-friendly, • Enhanced Parental Pay to support new families, • Referral Bonus to benefit from recommending talent #J-18808-Ljbffr

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