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An exciting opportunity has arisen for a Handyperson to join a educational establishment based in South West London. This will be on a 3 month contract. Duties include general maintenance duties around the campus and communal areas. • Changing taps • Changing door handles • Changing lights • PPM and reactive maintenance
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Role: Gas Install Engineer Location: Exeter Salary: £1,500 per week We are currently looking for experienced Gas Engineers to fulfil a gas Installation role for a market leading Gas Maintenance Company. This is an on-going sub-contract role with a minimum of a year`s work available and the capability of earning up to £2000 a week. All jobs are pre booked with the clients and are booked in the week before the gas installation is due to be completed. All work is booked via a PDA and the engineer will be completing between 3 and 5 boiler installs per week. All work will be based in the successful gas engineer`s preferred postcode area. The benefits to the successful gas engineer will be as follows: - Long term work - The opportunity to work for a market leading company - Training will be provided throughout the period of the contract to help improve skills if needed - Local and regular work through the summer as well as winter The successful engineer must be able to provide the following: - ACS qualifications - Gas safe card and certificate - Public liability insurance - A calibrated analyser - Own van insured for business use - Own tools - Relevant experience (2 years would be advantageous) - A minimum of one working reference Is this you? Then apply now by sending your CV to the gas team on (Email Removed) or contact us on (phone number removed)
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Role: Gas Install Engineer Location: Edingburgh Salary: £1,500 per week We are currently looking for experienced Gas Engineers to fulfil a gas Installation role for a market leading Gas Maintenance Company. This is an on-going sub-contract role with a minimum of a year`s work available and the capability of earning up to £2000 a week. All jobs are pre booked with the clients and are booked in the week before the gas installation is due to be completed. All work is booked via a PDA and the engineer will be completing between 3 and 5 boiler installs per week. All work will be based in the successful gas engineer`s preferred postcode area. The benefits to the successful gas engineer will be as follows: - Long term work - The opportunity to work for a market leading company - Training will be provided throughout the period of the contract to help improve skills if needed - Local and regular work through the summer as well as winter The successful engineer must be able to provide the following: - ACS qualifications - Gas safe card and certificate - Public liability insurance - A calibrated analyser - Own van insured for business use - Own tools - Relevant experience (2 years would be advantageous) - A minimum of one working reference Is this you? Then apply now by sending your CV to the gas team on (Email Removed) or contact us on (phone number removed)
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  • £100 - £160/hour Negotiable
Acting as a work-finding service, we provide supply cover to a range of Primary, Secondary and SEND Schools; from small village schools to large secondary schools. We are looking for Supply Teaching Assistants / Behaviour Support / Support Staff to cover all classes from Reception through to KS5 and who are passionate about education. Prospero Teaching are currently seeking experienced, dynamic and flexible School teaching assistants in Wakefield and the surrounding areas who are interested in working in a variety of client schools on a day to day supply TA basis. At Prospero Teaching we are looking for supply teaching assistants who are located in Wakefield and want daily supply work in that area. Due to the growing demand of our Prospero clients, we are looking to recruit a number of reliable supply SEN Teaching Assistants (primary teachers, secondary teachers & SEN teacher) with good behaviour management who are available for daily / short term supply or long-term absences. We will work around your schedule and preferences, so whether you are seeking a day's work here and there, or something more regular and consistent we will do our very best to help you as a teacher. CONTRACT/POSITION DETAILS: Location – Leeds Position – Supply Teaching Assistant / SEN Support Supply Type of work – Supply Teaching Assistant - day to day and long-term cover in various schools Start date – As soon as possible Duration / Likely Duration – Day to day bookings, with the potential for extension depending on schools End date (if applicable) – N/A Contract type - Temporary Full time/part time – Part time and full time depending on schools/supply teacher needs Minimum rate of pay – Minimum rate £65 per day Hours – 8:30 am – 3:30pm (full day) EXPERIENCE, TRAINING AND QUALIFICATIONS NVQ Level 3 in childcare or equivalent Previous experience working in a UK school TO BE ELIGIBLE FOR THIS ROLE THROUGH PROSPERO TEACHING, YOU MUST: Hold Right to Work in the UK Hold an enhanced child barred list DBS certificate registered with the online update service or be willing to process a new application Provide two professional related references OTHER: If you would like to be considered for this role, please apply with a copy of your up to date CV. Unfortunately, only shortlisted candidates will be contacted. Prospero Teaching is acting as an employment business/education recruitment agency in relation to this vacancy. The successful candidate will be required to register with Prospero Teaching in order to fill this vacancy. Prospero Teaching is able to offer the successful candidate: Free, accredited continued professional development courses including safeguarding and behaviour management In-house Training and Development Team
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  • £100 - £160/hour Negotiable
Acting as a work-finding service, we provide supply cover to a range of Primary, Secondary and SEND Schools; from small village schools to large secondary schools. We are looking for Supply Teaching Assistants / Behaviour Support / Support Staff to cover all classes from Reception through to KS5 and who are passionate about education. Prospero Teaching are currently seeking experienced, dynamic and flexible School teaching assistants in Wakefield and the surrounding areas who are interested in working in a variety of client schools on a day to day supply TA basis. At Prospero Teaching we are looking for supply teaching assistants who are located in Wakefield and want daily supply work in that area. Due to the growing demand of our Prospero clients, we are looking to recruit a number of reliable supply SEN Teaching Assistants (primary teachers, secondary teachers & SEN teacher) with good behaviour management who are available for daily / short term supply or long-term absences. We will work around your schedule and preferences, so whether you are seeking a day's work here and there, or something more regular and consistent we will do our very best to help you as a teacher. CONTRACT/POSITION DETAILS: Location – Doncaster Position – Supply Teaching Assistant / SEN Support Supply Type of work – Supply Teaching Assistant - day to day and long-term cover in various schools Start date – As soon as possible Duration / Likely Duration – Day to day bookings, with the potential for extension depending on schools End date (if applicable) – N/A Contract type - Temporary Full time/part time – Part time and full time depending on schools/supply teacher needs Minimum rate of pay – Minimum rate £65 per day Hours – 8:30 am – 3:30pm (full day) EXPERIENCE, TRAINING AND QUALIFICATIONS NVQ Level 3 in childcare or equivalent Previous experience working in a UK school TO BE ELIGIBLE FOR THIS ROLE THROUGH PROSPERO TEACHING, YOU MUST: Hold Right to Work in the UK Hold an enhanced child barred list DBS certificate registered with the online update service or be willing to process a new application Provide two professional related references OTHER: If you would like to be considered for this role, please apply with a copy of your up to date CV. Unfortunately, only shortlisted candidates will be contacted. Prospero Teaching is acting as an employment business/education recruitment agency in relation to this vacancy. The successful candidate will be required to register with Prospero Teaching in order to fill this vacancy. Prospero Teaching is able to offer the successful candidate: Free, accredited continued professional development courses including safeguarding and behaviour management In-house Training and Development Team
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  • £130 - £160/hour
A Thurrock based Academy are looking to appoint an outstanding primary teacher to join a hard-working and happy school. NQTs very welcome to apply. Key Stage 1 Teacher (with experience of Early Years) Required September 2019 This is an exciting opportunity for a passionate and motivated outstanding Key Stage 1 teacher to join a fun, dynamic, successful team. The school believe in providing a first class education and giving every pupil the best opportunities. The successful candidate will be an enthusiastic and ambitious individual who believes in the potential of every child and who will be committed to the Schools' ethos of high expectations, mutual respect and fun! You must be a team player and able to ensure that each child makes good progress. The children are well behaved, enthusiastic learners who want to achieve. Looking for someone who has the desire and drive to further their career and aspires to grow as a professional. Ideally like to appoint a high quality practitioner who has: A good understanding of effective learning and teaching and has high expectations. An imaginative approach to the national curriculum and can make learning fun and adventurous. The ability to inspire, motivate and challenge children. Good interpersonal skills and is able to work in a team collaboration with colleagues to provide the opportunities for children to make the best progress they can
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Skills • Demonstrate expert ability to design, manage, interpret and report clinical studies from Phase I to Phase III. • Demonstrate technical knowledge and innovation in clinical development study design that provides relevant evidence of progression from pre-clinical to clinical. • Strong track record of successful work leading to regulatory submissions for novel medicinal products to Competent Authorities that is supported by publications and references. • Experience of preparing and reviewing documentation for submission to Regulatory bodies including Investigator Brochures, Investigational Medicinal Product Dossiers, Clinical study protocols, Common Technical Documents, Paediatric Investigational Plans / Waivers, Marketing Authorisation Applications. • Practical working knowledge of relevant current ICH and EU guidelines / directives on safety, efficacy, quality and multidisciplinary topics, and currency with the changing regulatory landscape. • Expert practical working knowledge of relevant cGLP and cGCP regulations and familiarity with cGMP requirements. • Detailed first-hand knowledge and understanding of the drug discovery and development processes. • Broad professional experience obtained in appointments within the biotechnology or pharmaceutical sectors or regulatory authorities. • Able to work with the Dstl project team(s) and external project consultants. • Able to provide training and mentoring support and advice to clinicians within Dstl as part of good governance Duties • Provide expert advice, including provision of options and solutions, to support the generation of clinical strategies for novel medical countermeasures to chemical and biological warfare agents. • Provide expert clinical advice, including options and solutions, to broadly support development and future licensure of novel medical countermeasures. • Advise on clinical study plans, study design, regulatory requirements, and execution of clinical studies from first-in-human trials through to late-stage development studies. A working knowledge of cGxP requirements is essential. • Provide expert advice, analysis and interpretation of clinical data. Generate robust conclusions based on the data and provide options, solutions and recommendations to enable the execution of a concise and effective clinical development plan. • Provide third party expert advice and review of relevant non-clinical activities and data such that clinical development plans can be delivered to regulatory requirements. • Review protocols and data, and provide interpretations of data and recommendations for future work / experimental studies to support product development. • Prepare and review documentation for submission to Regulatory bodies including, but not limited to, Investigator Brochures, Investigational Medicinal Product Dossiers, Clinical study protocols, Common Technical Documents. • Provide advice and recommendations to ensure that the Dstl project team(s) deliver novel pharmaceutical products through the drug development process. • Act as a Subject Matter Expert mentor for Dstl staff supporting Clinical studies and Regulatory submissions within the Advanced Development Projects. • Challenge constrained thinking within the project teams and provide alternative solutions to problems that are consistent with current Regulatory guidelines. • Attend project team meetings / review meetings as required by the Dstl Project Teams. • Provide training and mentoring support and advice to clinicians within Dstl as part of good governance. • Commit to be available to respond to queries within a timely manner (typically within 5 working days). Background There is an enduring requirement for Dstl to support the development of Medical Countermeasures to chemical and biological warfare agents for MoD. A complex and changing regulatory environment exists for the provision of novel pharmaceutical products and on-going expert advice on clinical strategies and clinical study execution is required to progress and support new medicinal therapies through to licensure by Competent Authorities (e.g. Medicines and Healthcare products Regulatory Agency - MHRA and the European Medicines Agency - EMA)
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Scientific Challenges Specialist - Pharmaceutical/Translational research Clinician Location/Dept: Salisbury/Dstl We are looking for a SC cleared Pharmaceutical/Translational research Clinician who can demonstrate an expert ability to design, manage, interpret and report clinical studies from Phase I to Phase III. You will have expert practical working knowledge of relevant cGLP/cGCP/cGxP regulations and familiarity with cGMP requirements. There is an enduring requirement for Dstl to support the development of Medical Countermeasures to chemical and biological warfare agents for MoD. A complex and changing regulatory environment exists for the provision of novel pharmaceutical products and on-going expert advice on clinical strategies and clinical study execution is required to progress and support new medicinal therapies through to licensure by Competent Authorities (e.g. Medicines and Healthcare products Regulatory Agency - MHRA and the European Medicines Agency - EMA). You will have a MBChB, MBBS, MD or equivalent medical degree, have current professional registration with appropriate college & be registered with the GMC. Skills/experience required: * - Demonstrate technical knowledge and innovation in clinical development study design that provides relevant evidence of progression from pre-clinical to clinical. * - Have a strong track record of successful work leading to regulatory submissions for novel medicinal products to Competent Authorities that is supported by publications and references. * - Experience of preparing and reviewing documentation for submission to Regulatory bodies including Investigator Brochures, Investigational Medicinal Product Dossiers, Clinical study protocols, Common Technical Documents, Paediatric Investigational Plans / Waivers, Marketing Authorisation Applications. * - Practical working knowledge of relevant current ICH and EU guidelines / directives on safety, efficacy, quality and multidisciplinary topics, and currency with the changing regulatory landscape. * - Expert practical working knowledge of relevant cGLP and cGCP regulations and familiarity with cGMP requirements. * - Detailed first-hand knowledge and understanding of the drug discovery and development processes. * - Broad professional experience obtained in appointments within the biotechnology or pharmaceutical sectors or regulatory authorities. * - Able to work with the Dstl project team(s) and external project consultants. * - Able to provide training and mentoring support and advice to clinicians within Dstl as part of good governance Duties * - Provide expert advice, including provision of options and solutions, to support the generation of clinical strategies for novel medical countermeasures to chemical and biological warfare agents. * - Provide expert clinical advice, including options and solutions, to broadly support development and future licensure of novel medical countermeasures. * - Advise on clinical study plans, study design, regulatory requirements, and execution of clinical studies from first-in-human trials through to late-stage development studies. A working knowledge of cGxP requirements is essential. * - Provide expert advice, analysis and interpretation of clinical data. Generate robust conclusions based on the data and provide options, solutions andrecommendations to enable the execution of a concise and effective clinical development plan. * - Provide third party expert advice and review of relevant non-clinical activities and data such that clinical development plans can be delivered to regulatory requirements. * - Review protocols and data, and provide interpretations of data and recommendations for future work / experimental studies to support product development. * - Prepare and review documentation for submission to Regulatory bodies including, but not limited to, Investigator Brochures, Investigational Medicinal Product Dossiers, Clinical study protocols, Common Technical Documents. * - Provide advice and recommendations to ensure that the Dstl project team(s) deliver novel pharmaceutical products through the drug development process. * - Act as a Subject Matter Expert mentor for Dstl staff supporting Clinical studies and Regulatory submissions within the Advanced Development Projects. * - Challenge constrained thinking within the project teams and provide alternative solutions to problems that are consistent with current Regulatory guidelines. * - Attend project team meetings / review meetings as required by the Dstl Project Teams. * - Provide training and mentoring support and advice to clinicians within Dstl as part of good governance. * - Commit to be available to respond to queries within a timely manner (typically within 5 working days). As well as the specific experience required above you will have the necessary qualifications, skills & experience to take control of this requirement from its inception to its completion. If you meet the experience required above please call/mail me asap for more information. Thank you
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Freelance Medical Writer (Medical Education) I have an amazing opportunity for a Freelance Medical Writer to join my very popular Medical Education Agency in Central Manchester. We are working with an impressive Medical Education agency that have an outstanding reputation within the industry. The Medical Writer will be joining a fantastic agency, who have lovely chic offices based in Manchester. This is an interesting opportunity for a Freelance Medical Writer as they have a wide range of projects starting very soon. The Freelance Medical Writer (Medical Education) will be working on lots of interesting projects such as digital education, promotional medical education and traditional medical communications materials. Freelance Medical Writer (Medical Education) – Details 6 month contract Manchester – office based Day Rate – depending on experience. Full time The ideal Freelance Medical Writer (Medical Education) – will have the following A background in Medical writing in medical communications agencies Confident with assisting client calls & planning. Experience in the following areas; Respiratory, Devices, Rare disease, opioid dependence, GI, cardiovascular MSK, Allergy, Rare disease, Cardiovascular, Oncology. Experience in following materials; advisory boards, slides, excellence meetings. We expect this role to be highly popular, and the client is looking to interview from Wednesday 19th June – Friday 21st so we are keen to speak with ideal candidates immediately. If of interest, please apply here or email or call Tilly on (phone number removed)
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Pertemps Managed Solutions are recruiting on behalf of a government agency based in Glasgow who are looking to recruit a Transformation Programme Director PLEASE NOTE THIS ROLE FALLS OUTSIDE OF IR35 YOU MUST HAVE EXTENSIVE PUBLIC SECTOR EXPERIENCE TO APPLY The Role: The Programme Director will be responsible for delivery of the overall programme and the associated projects within the Transformation with a priority focus on the Technology related projects and programmes. This will include working with other SLC teams to deliver the changes required. This will include Finance, Commercial, Technology Delivery, Service Design, Architecture teams, Testing, Business Readiness teams from whom we will rely on support and/or who will dedicate members of their team to the programme. Job Purpose / General Characteristics: The responsibility of the role will include: - Design and delivery of the overall programme, approach and project plans to deliver the Transformation Setting up the programme with the appropriate teams, capabilities, partners, commercial, finance and governance Alignment of the programme with dependent changes across other portfolios and the wider SLC estate Assessment and prioritisation of projects to be delivered Management of 3rd party resources who will be delivering solutions within the programme and projects Sourcing, recruitment and development of the programme office, project and change management teams from both internal and external sources to deliver the components of the project Working alongside delivery teams to ensure projects stay on track and are delivered on time and to budget For more information please apply and a recruitment consultant will be in touch to answer any queries you may have
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