Uniting Holding

A leading hotel and spa in Newquay seeks a Food and Beverage Supervisor to lead the service team and ensure exceptional hospitality. The right candidate will have experience in food and beverage service and will support the recruitment, training, and financial performance of the department. This role offers a competitive salary of £21,626 per year and benefits like 28 days of holiday and live-in accommodation options. Join a dedicated team committed to quality service and a positive environment.

Company Description Bedruthan is a multi-award winning hotel and spa set into a cliff above Mawgan Porth beach on the North Cornwall coast. Our hotel has been cherished and nurtured by two generations of the same family for over 50 years to give our guests memorable holidays in this uniquely beautiful place. Bedruthan is set in a natural playground with the beach just below us and some amazing facilities at the hotel itself. You can stroll along the foreshore, get a surf lesson or two and walk the cliff path to Bedruthan Steps - one of the north coast's most dramatic beauty spots. Job Description We are looking for a Food and Beverage Supervisor to lead our fabulous team and support the 2 Assistant Food & Beverage Service Managers. Our F&B Supervisors ensure the cheerful and professional delivery of our food and beverage service to the required standards for the Wild Café and Herring restaurants on a daily basis by inspiring and enabling the team and leading by example. We are looking for someone who is experienced but also willing to learn, is self-motivated, works in a clean and tidy manner and is able to help lead our team. With potential for up to 800 covers throughout the day, including children, during busy seasons, this role is for the driven and not the faint hearted! You must be passionate about delivering consistent, impeccable service and hospitality to our guests whilst reflecting our relaxed approach. A personal licence would be an advantage. Key responsibilities Delivery of exceptional hospitality Support in the recruitment and selection of hosts Delivery of product knowledge and standards training to hosts Positive financial performance of Food and Beverage sales Guest data capture We offer £21,626 per year 45 hours per week 28 days holiday per year Temporary live-in accommodation available 50% discount on restaurant food during shift Free use of swimming pool and tennis court Access to gym Development and training Discounts on hotel services and products Many more perks Wish you were here? Please use the "apply" link to submit your CV and, in your covering letter, let us know why you would be the person for this role. You will need to confirm that you are eligible to live and work in the U.K. Direct applications only. As one team we take responsibility for reducing the negative impacts our actions and activities have on the environment and our local community; something we feel is right and is our way of life.

Field Service Engineer (North West) Reporting to - Service Manager Summary of role Healthcare 21 Group is a leading supplier of medical, diagnostic and critical care equipment across the UK and Ireland. Through its specialist divisions, including Xograph Healthcare and Aquilant Medical, the Group supports hospitals and clinics with life-support technologies, imaging systems and associated clinical solutions. This role combines responsibility for critical care equipment, including ventilators, respiratory and patient support systems; with imaging technologies such as C-arms, mobile X-ray and digital platforms. Working nationally, you will carry out installation, preventative maintenance, calibration and repair activities to ensure equipment performance, compliance and uptime in both critical care and radiology environments. The role requires a professional, proactive approach, strong technical capability and the ability to operate confidently in clinically sensitive settings. Full manufacturer and group training will be provided. Key responsibilities and activities Field Service & Repair Carry out on-site preventative maintenance, repair, calibration and installation across HC21 critical care and imaging systems Support life-support equipment including ventilators and respiratory systems Service imaging systems including mobile X-ray and C-arms Ensure compliance with manufacturer guidelines, IRR17 where applicable and company procedures Respond promptly to breakdowns to minimise clinical disruption Provide first-line remote diagnostics and technical support where required Technical Standards & Documentation Complete service reports, calibration records and regulatory documentation accurately and on time Record all activities using approved digital platforms Maintain controlled spare parts stock and specialist tools Ensure compliance with electrical safety, radiation regulations and infection control standards Support audit, quality and service KPI processes Customer Service Represent Healthcare 21 Group professionally at all times Build effective relationships with biomedical teams, radiology departments and critical care clinicians Communicate clearly, manage expectations and keep customers informed Work collaboratively with service support and operational teams to meet SLA commitments Flexible Working Support changing service demands, including occasional overnight stays and varied working hours Participate in on-call or escalation rotas where required Attend UK or overseas manufacturer training as required Work from home when completing administrative or remote support duties Essential & Key competencies Strong diagnostic capability across electrical, electronic and software-controlled medical systems Understanding of critical care and imaging equipment principles Ability to work independently in high-pressure clinical environments Customer-focused, organised and solutions-driven Professional, adaptable and resilient Key personal requirements HNC/HND or equivalent in electronics, electrical engineering, biomedical engineering or relevant experience 3+ years' field service experience within medical equipment preferredCompetent IT user with experience of digital service platforms National travel across the UK and occasionally Ireland Full UK driving licence DBS clearance (or ability to obtain) 40 hours per week, Monday to Friday, with flexibility aligned to service need What are some of the benefits of working at Healthcare 21? Lunch allowance. Company vehicle. HC21 training academy. Savings & Cycle Schemes. Remote/Flexible Working. Salary and bonus structures. Sustainable business strategy. Employee Assistance Programme.Pension, life assurance & income protection Long service awards & employee of the month Employee events & initiatives all throughout the year Enhanced sick pay scheme that increases with service Enhanced annual and life leave that increases with service We are proud to be an equal opportunity employer. At Healthcare 21 we know that diversity makes us stronger. We are committed to a collaborative, inclusive environment. We strive for everyone to feel valued, connected and empowered to reach their potential and contribute their best. We also know the confidence gap can often get in the way of meeting spectacular candidates, so please don't hesitate to apply - we'd love to hear from you!

Regulatory Affairs Manager We offer an opportunity to learn, progress and achieve, in a dynamic growing environment. The Company We are a growing international full service CRO company with an HQ in Guildford UK and major sites across the globe that offers its employees a genuine opportunity to develop, varied and interesting challenges, and recognition for achievement. Ergomed established in 1997 by two physicians in Croatia, provides expertise in drug development. Since this beginning, the company has grown to employ 700 people worldwide including its division of PrimeVigilance and is listed on the LSE. Our clients value us for our scientific and medical expertise and we have one of the highest client retention rates in the industry. Our innovative site management and study physician model set us apart from our competitors. Helping to develop drugs that improve patient's lives is our passion. The Position We are looking for a Regulatory Affairs Manager, to be based in UK, Germany, Poland, Croatia office or home based. We offer the chance to work in a small but growing team of around 8 people in a wide range of projects and therapy areas, and across all phases. We offer a friendly professional working environment. We offer a competitive salary plus a good benefits package. Requirements Proven experience of leading the regulatory aspects of clinical studies on an international basis. Some experience of leading small project teams, and line management of regulatory associates. Ability to cope with the demands of multiple projects. A minimum of a science based Bachelors degree with a higher level qualification preferred. Responsibilities Assume responsibility to act as Lead RAM for a study, as assigned by the Head of RA department, and be responsible for the regulatory management of that trial which includes development of Regulatory Management Plan, study specific FMEA and final review of CSR from regulatory aspects. To provide regulatory training to more junior regulatory staff. Evaluate / summarize data; prepare and submit documentation related to clinical studies (CTA, any amendments, end of study notifications, study progress reports, CSR submission etc.) to the relevant regulatory authorities, and act on the Sponsors behalf in liaising with these authorities. Primary point of contact for the Sponsor's regulatory group. Responsible for requesting / receiving all Sponsor's regulatory documentation to support the Clinical study application. Location You can be office or home based in any country we have an office. Why Should You Apply? You want to be involved in a wide range of interesting projects and studies. You want your achievements and hard work to be recognized. You want to work for a growing company where you can progress in your career and where there are opportunities for advancement. You want to work in a company that has a great reputation with its clients and employees, and invests in its relationships with both.

A growing international CRO company is seeking a Regulatory Affairs Manager to oversee regulatory projects across various therapy areas. The role involves leading clinical study regulations, providing training to junior staff, and liaising with regulatory authorities. Applicants should have experience in regulatory affairs on an international scale and hold at least a Bachelor's degree in a science field. This position offers a competitive salary and opportunities for career advancement in a dynamic environment.