4591 Science jobs

Fantastic Monitoring Opportunities - Field/Home based - UK I am looking to identify talented CRA's to discuss some exciting opportunities I am recruiting for, for an international company who have a very strong pipeline of trials with some of the biggest and most innovative sponsors. I am keen to speak with Clinical Research Associates who have a minimum of 18 months, independent monitoring experience who are keen to expand their skills and discuss opportunities with a company that will help develop you and offer a very clear career path for your future progression. My client has a range of opportunities including both CRA II and Senior CRA as well as site management positions supporting a range of Sponsors on some very interesting and niche Clinical Trials. The Senior opportunities would include additional responsibilities such as team organisation and leadership of more junior CRA's and would need someone who has full trial life cycle management experience from start up through to Close out. My client would be looking for a minimum of 3 years independent monitoring experience for their Senior positions. This company will provide regular training and key support from an experienced line manager as well as more senior staff. In addition to the independent monitoring experience, I am looking for CRA's who have a life sciences degree, have worked for a CRO or Pharma company and can happily travel to sites right across The UK for monitoring visits and be comfortable working from home the rest of the time. If this opportunity sounds of interest and you have the right experiences I am looking for, then please get in touch. If you do not feel that your skills are quite right, please still reach out to me as I am working many different opportunities and I may have something else suitable for you. My name is Alex Goodman and I solely recruit Clinical experts and have connections with several large and small organisations who are always looking for high calibre talent to join their exciting teams. If you work in any Clinical function and would like to discuss potential new opportunities, please do not hesitate to contact me. At RBW Consulting Ltd, every one of our consultants has one specific area of expertise ensuring they excel in helping Life Sciences Professionals find the jobs they are looking for in the industry. With unrivalled industry knowledge and excellent links with hiring managers in Biotechs, Pharmas and CROs throughout the UK, Europe and across the world, we would be delighted to speak with you about the role you are looking for...... click apply for full job details

Are you interested in leading a team in medical image analysis in neuroscience? Our client is a leading medical data analytics company, providing data management and advanced analytics to the pharmaceutical clinical trials market. They need a supervisor to lead their growing team - this will include remote team leadership. Purpose of the Role: The Image Analyst Supervisor is a new operational team supervisor role, responsible for supporting the imaging team with operational delivery. This includes management of a team of Image Analysts (IA), and the day-to-day supervision of data quality checks (QC), site management (SM) and image analysis (IA) activities across all projects to meet agreed milestones and targets. The key success criteria for the role are the effective management of a team of IAs working predominantly remotely in a fast-paced environment, maintaining open and positive communication to ensure adherence to procedures and coordinate training to increase capability and efficiency, and collaborative working with colleagues in Project Management, Data Management, Science and Technical Support functions, as well as external contacts at clinical trial imaging/data collection centres. Responsibilities: Line management and daily oversight of IAs including setting tasks and targets and monitoring and reporting against these targets. Train, mentor and support IAs to be able to work across projects Performing image analysis, such as whole brain delineation and endpoint QC, after suitable training has been completed. Ensuring team compliance with Policies, SOPs and other working practises. Forecasting and resource planning for analysis and site management deliverables to meet agreed budgets and forecasts. Assist with setting, monitoring and achieving KPIs and efficiency targets to meet customer expectations and turnaround times. Coordinate training for team members to increase capability and overall efficiency in QC, IA and SM. Provide regular progress reports on deliverables and any issues arising, including conflicting priorities and available capacity. Provide performance feedback, workload balancing and coaching of team members. Providing suggestions and implementation for continuous improvements in QC, IA and SM processes. The Image Analyst Supervisor may also be responsible for: Providing site support for imaging related questions, data upload and technical issues. Qualitative review of images (MRI, PET, CT etc), identifying any problems which may affect subsequent quantitative analysis or radiological review. Qualifications and skills: Essential Bachelor's degree (imaging or life sciences) or equivalent scientific or analytical experience. Proven experience in a similar role, with team and line management experience. Good understanding of clinical research phases and the processes involved in the planning and management of a clinical trial. Evidence of quality compliance and continuous improvement within areas of responsibility. Intermediate to advanced in the use of Microsoft Office software applications and clinical data management systems. Desirable Good understanding of anatomy and its presentation within various imaging modalities...... click apply for full job details

We're looking for a candidate to fill this position in an exciting company. Develop and conduct GEP Studies Provide technical expertise to Commercial Team and liaise with external partners. Ensure adherence to relevant regulations and guidelines - GEP, GLP, EPPO. Train and maintain Junior staff Practical experience in a similar commercial/industrial setting working to GLP/GEP/EPPO regulations. Understanding of the agrochemical industry and Agricultural market.

We're looking for a candidate to fill this position in an exciting company. Develop and lead GLP Studies Data interpretation and technical report writing. Ensuring adherence to relevant guidelines and regulations. Carrying out Analysis when required. BSc in Chemistry or similar relevant discipline Experience as Study Director for GLP Studies. Experience with chromatographic techniques, particularly HPLC and GC Experience with Agrochemicals or in a similar , related industry.

Vacancy Information It is East Lothian Council's policy that successful applicants will be placed on the first point of the salary scale. This post is term time - 39 weeks per year Days and Hours of Work: Mon-Thurs 08.15-16.30, Fri 08.15-13.15 (less breaks) with some flexibility To start October 2020 Ross High School, Tranent is conveniently situated close to the A1 in East Lothian and serves a widespread community including towns and villages of Tranent, Macmerry, Ormiston, Pencaitland, Elphinstone, Humbie and Saltoun. The school provides education to a student population expected to raise in the next few years. Led by the Head Teacher and committed teaching staff, the school has a progressive philosophy and aims to unlock students' potential by: Encouraging achievement Rewarding success Developing responsibility Promoting respect For the right individual, the school offers both the environment and the opportunities for exceptional professional development for an ambitious teacher. Job Details To assist the Science Technician in preparing practical experiments and paperwork for the science classes. The job also involves cleaning and maintenance of equipment within the science department. The Jobholder is responsible for ensuring that equipment is available for use by teachers and students. Please download the Job Outline/Person Specification (available under 'Job Attachments') for the full range of tasks and duties associated with this job. You will need to refer to these in order to complete the application form. You must ensure you meet every 'essential' criteria stated on the Person Specification to be considered for interview. The 'East Lothian Way'- values and behaviours we expect our employees to demonstrate in their everyday work. Should you be invited to interview, you may be asked questions based on these behaviours. Please refer to the document via the link to familiarise yourself with them. Job Requirements Relevant Qualifications Educated to SVQ2, National Certificate, Higher or equivalent in a relevant discipline. and/or able to demonstrate equivalent knowledge, skills and competencies gained through relevant experience. PVG Membership This post is considered as Regulated Work with vulnerable children and/or protected adults, as specified in the Protection of Vulnerable Groups (Scotland) Act 2007. All preferred candidates for posts carrying out regulated work with these groups will be required to become a PVG Scheme member, or undergo a PVG Scheme update if they are already a member, prior to any formal offer of employment being made by East Lothian Council. Please note: PVG member's records are constantly updated with any new vetting information that arises. Any information that is disclosed on a PVG membership or update check, if relevant to the post being applied for, will be discussed with the applicant and investigated prior to any formal offer being made. Please note: If you have spent more than 3 months working or living outwith the UK in the last 5 years then you will be required to present a copy of an overseas criminal record check. Details of how to apply and contact details can be found on the GOV.UKwebsite. Additional Information For additional East Lothian Council employment information please click on the following link: If you have any difficulties creating an account on MyJobScotland or applying for this post please contact the MyJobScotland support team via this link . If you require further information about this vacancy, please call , or email us on Please note: we do not accept CV's. There is no function to allow you to upload a CV to MyJobScotland and we do not accept CV's by post or email. All our vacancies must be applied for by completing the on-line application form...... click apply for full job details

Advert You will be required to provide a science technician service within the school, servicing Biology, Chemistry and Physics laboratories by ensuring that all equipment and chemicals required are properly prepared and available in a safe and functional condition. An appropriate science based qualification (i.e. chemistry, biology or physics) at C&G/ONC/HNC level, or equivalent, is essential. In addition you should have experience in the care, use and maintenance of science equipment and have an awareness of current health & safety practices. This post is considered Regulated Work with Children, under the Protection of Vulnerable Groups (Scotland) Act 2007. It is an offence therefore to apply if you are barred from working with children. Employees with a contract of employment for 3 months or more are automatically included in our Local Government Pension Scheme which is a career average scheme. Pension contribution rates are based on a tiered system determined by your annual full time equivalent pensionable pay. For example for those earning up to and including £21,800 the contribution rate you pay is 5.5% of your salary. The council pays the rest of the cost of providing your benefits. This amount varies but it's always enough to make sure your pension can be paid and will be at least 19.3% of your pay. In addition you get tax relief on your contributions - the tax you pay on your salary is calculated after your pension contributions are deducted. Other main pension benefits include a pension that increases each year in line with price inflation and the ability to exchange some of your pension to provide a tax free lump sum. Further details can be found in the attached document General Information for Applicants or via the Strathclyde Pension Fund website . Additional Information Please click on the attachments below for full details of this post...... click apply for full job details

SCOPE OF ROLE: Lead and direct the in-house creative team, to create and deliver UK and IE sites for all Yours Clothing brands on & offline. Working with the UK Creative Manager to ensure brand consistency and brand development across all channels and all product categories. Execute cross-platform design, with priority of mobile design, but designing for Desktop, Mobile. Tablets and Apps. KEY RESPONSIBILITIES: Branding Develop and own the implementation, updates and adherence to the creative guidelines including, but not limited to, tone of voice. Work with internal stakeholders to agree and ensure consistency of the brand and setting the expectation at the highest levels of quality for all areas of creative, keeping in mind key values and the global reach of the business. Sign off artwork to ensure consistency Project management Assist project teams across the business adding both creative input and solutions to help agree, maintain and communicate timeframes based on the resource available and workload priorities. Organise work flow within the creative team efficiently to meet deadlines and adapt to changing business demands as required. Work analysis Using data insight and feedback from key stakeholders, Report back on performance of work achieved by the team. Keep up to date with current fashion trends. Research competitor and high street retailers' websites and stores to stay ahead of competition. Analyse all YC sites to help develop UK ideas and concepts that drive traffic and improve customer journey/experience. This includes development of best practice landing pages and testing of UK design initiatives. Leadership and mentoring Provide leadership, support and development to the team ensuring positivity and creativity is fostered, encouraged and maintained. Management Manage UK design team through effective performance management and motivation. To include regular 121s and effective communication, delegation and motivation along with ensuring that they are effectively resourced and everything they need to complete their work. Coach and encourage creative and professional development. Resource and staffing Lead the continuous improvement of the UK design workflow by directing, taking ownership and implementing changes to benefit the team and the business...... click apply for full job details

Scope of the Role Are you interested in the retail fashion industry and have experience in InDesign, Photoshop, and have HTML knowledge? We are looking for a creative, forward thinking individual to join our Design team as a Graphic Designer. This is an ideal opportunity for someone looking to take the next step in the career. You will be involved in the design, update & upkeep of our international e-commerce sites as well as online and offline marketing design. You will be an excellent communicator, able to work face to face, on the phone and through email. You'll have a meticulous eye for detail, and a keen understanding of our target audience. With a strong work ethic and the ability to deliver a balanced workload to achieve targets and deadlines, you'll be a welcome team player, in a dynamic working environment. Key Responsibilities: Homepage & Landing Pages: Working with the design and marketing teams to create new concepts, and execute layout and concepts. Working collaboratively with the Creative Manager and the rest of the design team on weekly site refreshes. Understanding multi-channel design, with priority of mobile design. Email marketing: Designing email newsletters with a trading/marketing focus. Gathering translations from the in-house translators and creating artwork. Building email newsletters using our ESP. Responsible for proofing and signing off all emails. Everyday: Think creatively to produce new ideas and concepts. Working with our in-house translators to update any UK graphics for our international customers Keep up to date with what competitors in the market are doing. Identifying opportunity to utilise new channels and technologies. Analysis of current site to help develop creative ideas and concepts to drive traffic and improve customer journey/experience. Skills and Qualifications: BA(Hons) in Graphic Design or related field. Adobe CS - InDesign, Photoshop, Illustrator, and CMS. Excellent core graphic design, typography, layout and digital standards. Experience designing cross-platform (in fashion or lifestyle preferably) - understanding the specifics of designing for Desktop, Mobile, Tablets and Apps. Interest in Fashion and eCommerce. Meticulous attention to detail Key Attributes: Excellent organisational and communication skills. A strong work ethic and innovative approach to all tasks Proven ability to work well within a team and to use own initiative An energy and enthusiasm to succeed Ability to work under pressure and work across multiple projects...... click apply for full job details

A luxury beauty brand in Liverpool are seeking a very talented digital designer to help oversee the creative design for the brand working alongside the talented creative and marketing team. Located slightly north of Liverpool City Centre, in very modern bustling offices; you will be working as a Digital designer with opportunity to have plenty of creative freedom, help in leading the creative direction with 2 other graphic designers over beautifully crafted eCommerce campaigns over digital and print. You will be responsible designing captivating digital campaigns for desktop and mobile. This will also include captivating social media campaigns to help promote their latest trends and products. Additional responsibilities will include; MailChimp emails, designing look books, adverts, and weekly newsletters as a well as working with their art directors and production team on international fashion shoots! To be successful; you will have ideally 3+ years experience with a great understanding of fashion/beauty eCommerce design - working on clean and considered design layouts and graphics. Having a strong understanding of social media campaign graphics, basic knowledge of HTML/CSS and responsive design an advantage but not necessary. This is a very unique opportunity to join a prestigious and high-end international fashion brand with a great central location and an array of great staff benefits and amazing international team socials. They are interviewing immediately, please apply with your CV and Portfolio asap...... click apply for full job details

Johnson Matthey are currently recruiting for two Senior Scientists. This is an exciting opportunity to join Johnson Matthey's rapidly expanding Battery Materials business, which is a material science and electrochemistry-based business with global reach. This role will be at the heart of the activities focused on development and manufacturing of advanced materials for the fast-growing battery market, working in a lean team with a start-up mentality driving to become a world-class large-scale producer. The purpose of these roles is to lead development of the scientific understanding necessary for eLNO process design. The process designs will be implemented in major new capital projects for the Battery Materials business. In this role you will lead a team of scientists in developing viable processes for the production of high purity base metal solutions from a range of impure raw materials, based on sound scientific knowledge and understanding through internal experimentation, literature research and external collaboration. Key responsibilities · Ensure hazards associated with all project activities are identified and managed.Carefully plan and manage experimental work to ensure full EHS compliance, including close liaison with offsite teams to plan the work, preparation of COSHH and risk assessments, and close attention to detail during the work itself. · Formulate and oversee experimental programmes to inform process development and scale up to large scale production. · Produce, analyse and synthesise scientific data to help inform and direct optimisation of critical processing parameters. · Collaborate with the engineering team to investigate process parameters to support process design · Report findings to the wider team in compelling, concise and accurate reports, presentations, discussions, etc · Plan and conduct work to deliver process scale up projects against financial, quality and time metrics, to meet the committed timelines for the JMBM business plan as documented and monitored through the PMO. · Provide technical knowledge for quality assurance processes such as FMEA's · Actively promote and facilitate meaningful exchange of information between scientists and engineers to optimise product manufacturability and economic scalability of process choices and to accelerate implementation at all production scales. · Proactively seek synergies or learnings from other parts in the JM organisation that may have experience in related processes and technology platforms. Are you the ideal candidate? You will: · Be educated to degree level in chemistry or a related scientific subject...... click apply for full job details

Do you crave to work in a fast-paced and dynamic environment where you will be contributing to a growing company? is the world's leading contract provider of topical and transdermal product design and development services. We are currently recruiting for a Junior Process Development Scientist to join our Process Development & Production team based in Guildford, Surrey. A Junior Process Development Scientist will be responsible for assisting Scientists with the execution of projects within the set timeline. You will also perform predefined experiments as outlined in the study plans, whilst always ensuring that you work in compliance with the GxP regulation and MedPharm's QMS. This is a temporary, fixed term position to assist our department with projects during a busy period, with a view of starting immediately. Responsibilities: Assist the Scientist / Senior Scientist in executing projects in accordance to the study plan, experimental designs and SOPs, in agreed timelines and in compliance with MedPharm's QMS. Maintains cross-functional communication with the internal stakeholders of the project. Review literature in preparation for studies and to regularly update knowledge by reviewing appropriate literature. Characterise formulations during development phase and on developmental stability studies and Tox batch release. Undertake general waste disposal and contribute to the general tidiness and cleanliness of the laboratory environment Raise and complete relevant documentation pertaining to the ordering and purchasing of equipment for the department. Applicant requirements: University degree in a related field (biotechnology, pharmacy, chemistry, chemical engineering etc.)...... click apply for full job details

Do you crave to work in a fast-paced, dynamic and team environment where you will be contributing to a growing company? MedPharm has clients spread throughout the globe and is the World's leading contract provider of topical and transdermal product design and development services. We are currently recruiting for a Projects Assistant to join our Project Management team based in Guildford, Surrey on a full-time, permanent basis. Responsibilities will include: Coordinate and prioritise varied administrative and development activities for team members. Drafting of project documentation on behalf of the Project Managers Supporting the Project Managers in tracking project progress to ensure milestones are achieved Help determine time, cost, resources and materials to complete a project Build relationships with internal/ external stakeholders and manage expectations accordingly Collating monthly KPI's Coordinating with the business development, resourcing and finance teams to drive revenue growth Drafting of presentations for client meetings Attending client meetings, taking meeting minutes for the Project Managers and following up on meeting actions ...... click apply for full job details

Company description: Your new employer is Covance Inc., the drug development business of LabCorp®, is the world's most comprehensive drug development company, dedicated to advancing healthcare and delivering Solutions Made Real®. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow's challenges as they evolve. Covance are seeking a Clinical Research Technician to join the Clinical Pharmacology Team within the European Centre of Excellence in the heart of Leeds, West Yorkshire in a bank position. You do not need a medical/scientific background for this position, we will provide you with comprehensive training and support. You will need a flexible approach to working as this position will include day/evening/weekend shifts. This will be "on-call" type of contract. Job description: Your primary responsibility will be to take biological samples from staff and healthy volunteers as part of Covance's COVID-19 testing programme, completing the required paperwork and preparing test samples for shipment. Your responsibilities may include but not be restricted to: Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings Preparation and accurate recording of ECGs/Holters Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples Monitors meals to ensure dietary compliance by research participants Assist in the preparation of rooms and medical equipment Assist with screening procedures as needed Maintain a clean, safe, and efficient working and study environment Foster respectful relationships with study participants Accurately record all research data obtained or observed Assist with QC of source documents and case report forms Maintains a constant awareness of participant safety and dignity at all times. Handles participant complaints efficiently and effectively in order that their satisfaction is maintained. Required profile: Education - a good standard of general education, particularly in science subjects. Experience - previous clinical research experience would be advantageous. What we offer: Covance is proud to be an Equal Opportunity Employes. As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status...... click apply for full job details

Interim Senior Interaction Designer Pay Rate: Up to £550 per day pay range, subject to IR35 status Responsibilities As an interaction designer you will: understand user needs and design services that meet them design user-centred interfaces and transaction flows define elements - layout, design patterns, controls and actions define visual priorities - what needs to be obvious, what needs to be easy, and what needs to be made possible create and rapidly iterate prototypes to help the wider team learn about user needs for different scenarios or tasks work with product owners, other designers, user researchers, business analysts, and front-end developers to turn concepts into user-centred services make sure that the design of services is consistent internally and with the rest of GOV.UK contribute to designing interaction patterns and standards, looking for common features across services take responsibility for creating and keeping up a positive and collaborative working environment contribute to building a digital culture in the department play an active part in the department's product design community Skills and experience required You should: have relevant industry experience understand the web have experience of working from a digital perspective have experience of sketching, prototyping and iterative design have experience of working in a multidisciplinary team have experience of using a user-centred design approach have experience of explaining design decisions and communicating ideas in a way that other people understand be able to lead a workshop be able to help the design process work effectively know how to plan user research have experience of interpreting research and data have experience of handling constructive criticism of your work have experience of constructively reviewing other people's work have experience of putting forward the case for design to senior stakeholders and product owners have experience of working at pace in an agile environment Contract Length: 6 months "Essential Requirements" - Please check to ensure that your CV addresses the following items: Our clients are generally seeking applicants who are reasonably local, so on that basis we would ideally like you to supply us with your address (or at least your post code) and a telephone number so that we can reach you during working hours. Your recent UK working experience going back at least 5 years, or full employment history if you have been working for fewer years than this. Your availability to work either immediately, or at short notice...... click apply for full job details

Freelance CRAs - various locations across Europe I have had some initial discussions with a niche Clinical Research Organisation who are pipelining for some future trials and are keen to have a small group of international freelancers across Europe for monitoring these trials once they are given the go ahead. At this moment in time I am keen to speak with freelance CRA's who have availability for monitoring over the coming months. This does not need to be a full FTE availability as I do not believe this company will need this. If you are based in the UK, or mainland Europe then please get in touch for more information about these opportunities. The company have a preference for CRAs who can perhaps monitor in more than one country for example, Belgium and the Netherlands or Spain and Portugal. Day and hourly rates are competitive and this may become more regular work as time goes by and the company are able to introduce more and more trials. Please reach out to me for more information, my name is Alex Goodman and I have a number of opportunities with organisation across Clinical Research and I am keen to find out what I can help you achieve in your career...... click apply for full job details

If you are a CRA looking for reduced travel, better progression opportunities and a supportive company with a very impressive pipeline of projects, then I have the perfect regional opportunity for you which covers all of those bases and more! If you are based in or around the Liverpool, Thames Valley, Wales & Newcastle regions and are currently looking for something that offers more localised site travel, then please get in touch, these positions won't be available for long. If you like the sound of this opportunity but are not within these specific locations then do not count yourself out as I am confident that there may be alternative opportunities that I can discuss with you. In addition to localised travel this position also offers excellent development opportunities and is an organisation who have won several awards for Excellence in CRO Leadership as well as for their Training for both new and experienced clinical professionals worldwide. There is no time like the present so for further information please get in contact! Speak to Reece on (0) to find out more...... click apply for full job details

HV Electrical Design Engineer Full-Time / Permanent Durham £60,000 (up to depending on experience) IMMEDIATE START FOR THE RIGHT CANDIDATE Do you have experience as a HV Electrical Protection Design Engineer? Can you lead projects up to 1 million pounds? ABOUT YOU · Minimum of 3 years' experience within the industry · HNC in Engineering discipline · Understanding of Document Management and Control · Experience of Numerical Protection Relays - Siemens and GE (Alstom) · Experience of Panel Function Testing · Clients / Sub Contractors and Suppliers · Supervising teams · Design experience - Electrical Protection / Substation Design DESIRABLE · Understanding of Electrical System Fault Analysis Software · AutoCAD design BENEFITS · Career progression · Flexi working - Can work from home · Free parking · Private healthcare · Training · Company events · Relaxed casual dress If you would like to be considered for this opportunity, please do email with your CV in the first..... click apply for full job details

Role: CAD Engineer - Water sector Location: St Austell Rate: £30 - £35 per hour - Ltd company or Umbrella Duration: 6 Months + Start Date: ASAP Are you an experience CAD Engineer within the water sector looking for your next long term contract. Responsibilities include: ·Preparation of Flowsheets and Piping & Instrumentation Diagram's ·Preparation of 3D models ·Preparation of site layouts and General Arrangements ·Preparation of pipe work detail drawings and Bills of Material ·The use of Plant P&ID/Plant 3D/Revit/AutoCAD to produce the above models/drawings ·Carry out site surveys ·Carry out 3D laser scanning on site, and stitch Pointcloud outputs using proprietary software ·Co-ordinate & liaise with other internal and external mechanical, electrical, civil designers, sub-contractors & suppliers ·Assist with the design verification & validation processes, including attending design reviews. ·Evaluation of potential hazards through design risk assessments Skills and experience: ·Autodesk AutoCAD experience essential ·Autodesk Revit experience essential ·Autodesk Plant3D experience beneficial ·Knowledge of BS19650 (BIM Standard) workflows - specifically how models/drawings operate under these standards beneficial ·Experience in a process industry design role preferred If you are interested you can apply on online or send your CV to and I will call you to discuss By applying for this position you are agreeing for Carrington West to hold and process your personal data in accordance with our Data Protection Policy. Your data will be shared with third party clients specifically relevant to any roles you have applied for...... click apply for full job details

If you are a CRA looking for reduced travel, better progression opportunities and a supportive company with a very impressive pipeline of projects, then I have the perfect regional opportunity for you which covers all of those bases and more! If you are based in or around the Liverpool, Thames Valley, Wales & Newcastle regions and are currently looking for something that offers more localised site travel, then please get in touch, these positions won't be available for long. If you like the sound of this opportunity but are not within these specific locations then do not count yourself out as I am confident that there may be alternative opportunities that I can discuss with you. In addition to localised travel this position also offers excellent development opportunities and is an organisation who have won several awards for Excellence in CRO Leadership as well as for their Training for both new and experienced clinical professionals worldwide. There is no time like the present so for further information please get in contact! Speak to Reece on (0) to find out more...... click apply for full job details

Westwards Labs is part of the Samworth Brothers Group, a 4th generation family business that prides itself on looking after its people and producing high quality products. We are always looking for outstanding people, with great attitudes and an openness to learning to join our family. The size of our business enables us to support career development and progression that will help our people fulfil their potential. Job Opportunity To carry out microbiological analysis of food and other materials, practicing aseptic technique and complying with the standards and principals set out in the Microbiology and Quality Manuals. Undertake tasks related to testing, promoting efficient workflow and a hygienic work environment. To ensure that the accreditation requirements of ISO 17025, M&S and TLAS are followed at all times. Microbiological testing of samples, which includes the sample preparation and plating, plate reading and interpretation and confirmation. The testing and related tasks must be carried out aseptically, following the methods described in the Microbiology Manual and the principles set out in the Quality Manual. The work is generally tackled as a team effort and analysts may undertake a variety of tasks within the day to provide optimum work flow. Perform scheduled equipment checks and take appropriate action when equipment is not functioning correctly. Complete equipment monitoring records. Undertake cleaning and hygiene operations during and at the end of the working day ensuring a high standard of personal cleanliness, maintaining clean equipment and workstations and proper disposal of laboratory waste. Participate in internal and external quality control programmes. Preparation of media when extra assistance or holiday/sick cover is required in this department. Records results on LIMS and identify out of specification results and suspect Listeria and Salmonella detection to the appropriate Manager. Report contamination, anomalous results or other internal anomalies to Manager. Report any other internal anomalies to a Manager. Demonstrate to other staff test of procedures in which you are fully trained and experience and supervise trainees work until you judge them to be proficient and aware of the critical points. Observe the security procedures applicable to the results and data produced. Answer telephone calls referring enquiries to the relevant person. Maintain a professional approach at all times working alongside and supporting the team and management at all times. Set an example in your behaviour and work for other members of staff. Good service is part of the company's philosophy and as a customer focused industry all customers must be dealt with professionally as customer satisfaction depends on the whole of the team. Ensure you act as part of the team and not just as an individual by good communication, cooperating and sharing skills. Promote a posting and praising culture both vertically and horizontally within the team framework at the laboratory. Communicate your ideas and problems and help the business achieve better solutions. Be responsible for health and safety in the department and enforce safe practices of work and raise concerns with the Health and Safety Representative and or more Senior Management. The Right Person You will be someone who is self-motivated and focussed on the customer. You will demonstrate initiative and ownership. You value others and their contribution and enjoy working collaboratively with colleagues. You will be flexible and adaptable to change. In addition, you will have the following skills: Two A level passes in science based subjects for five GCSE's (Grade C or above) Laboratory experience Current Driving Licence Evaluation skills Knowledge of security requirements Experience of equipment operation and check procedures Effective team player We provide a terrific range of benefits including great facilities with onsite parking and subsidised restaurants, as well as an excellent retirement savings plan (pension), private health cover (subject to terms and conditions) and a discount scheme 'Quality Life' that provides savings at supermarkets, high street retailers and a host of leisure outlets...... click apply for full job details

Biomedical Scientist - Virology (Band 5/6 equivalent) The London Clinic is one of the UK's largest independently owned non-profit hospital, where we pride ourselves on our values, and putting the patient at the heart of everything we do. We have an exciting opportunity for a Biomedical Scientist to join the Virology team located at 116 Harley St, Marylebone, London W1G 7JL. The London Clinic is one of the UK's largest independently owned non-profit hospital, and we have been providing exceptional care since 1932. We have 8 premises, where we perform highly complex procedures as well as routine surgery & medicine. The London Clinic is the largest independent establishment to provide Stem Cell Transplant services and is the busiest UK and European independent collection centre for donor registries. The Virology lab is responsible for testing all of the Stem Cell and Bone Marrow Donor bloods for infectious disease markers. To uphold the excellent reputation to date, it is imperative to provide a robust and resilient service which is critical in nature Job Profile: You will facilitate the provision of a co-ordinated, high quality inpatient service to cancer patients. Job Type: This is a full-time, permanent position working 37.5 hours per week. The working pattern will be 8pm - 8am Monday to Wednesday plus rotational weekly over time. The post holder for this role will need to be flexible as the service will return to a Mon - Friday 9am - 5pm pattern in the future. Salary: The salary is competitive for this role and will be dependent upon skills and experience. Benefits package: We offer a comprehensive package which includes a contribution pension scheme (total annual contribution up to 17%), Private Medical Healthcare, 25 day's annual leave, season ticket travel loan, and a wide range of discounts with a variety of retailers and services. We also offer excellent career development; with clear career pathways and access to further education. Duties & Responsibilities To support the Virology Lead in the duties outlined below: Formulation of policies and procedures and standard operating procedures for the efficient testing for molecular virology and serology. Reporting, discussing and communicating test results and complex analytical data with consultants. Reporting test results accurately and in a timely manner. Performing specialised operation, setup, maintenance and fault finding on analytical laboratory equipment ensuring continuity of service. Keeping good, organised and complete records of all cellular material passing through the laboratory, both electronically and paper copies. Preparing information for formal presentation at sectional, departmental and all meetings relating to the transplant centre. Implementation of emergency procedures as appropriate. Arranging for cell analysis or processing to be completed by external laboratories if required and assisting with technical agreements between other hospitals and services providers. Laboratory participation in service-related research and development projects. Skills & Experience Biomedical Scientist (BMS) with HCPC registration Experience working within a Virology Laboratory Highly motivated individual who possesses strong communication & organisational skills. Effective interpersonal skills with the ability to work independently and as part of a team. The London Clinic is proud of its diverse workforce and is committed to building a team that represents a variety of backgrounds, perspectives, and skills. We absolutely welcome applicants from underrepresented groups; if you think you have the skills and experience for the job, please apply - we would love to hear from you regardless of your background...... click apply for full job details

MEDICAL DEVICE QA SPECIALIST Reporting to the QA/RA Manager, you will be responsible for ensuring continued compliance and improvement of the Quality Management System of the company with the relevant European Medical Device Regulatory requirements, and to ensure that these are continually maintained and implemented in the best way possible. You will be expected to work independently and be accountable to deliver against agreed deliverables in a fast-paced small business environment and have the opportunity to innovate and contribute as part of a small QA/RA team, working closely with the QA/RA Manager and an RA Specialist. This full time and office based position is suitable for an individual who is a self-starter, passionate about quality and can immediately add value to the organisation. Responsibilities Provide day-to-day support and be responsible to maintain the effectiveness of the quality management system, including document control, CAPA, Vigilance, Risk management, internal audit, post-market surveillance, supplier monitoring and assessment and product release activities Contribute to strategic improvement projects to improve business processes and the implementation of MDR (EU) 2017/745 Prepare and present quality data to analyse quality trends and support investigations, remediation and improvement initiatives Competencies Highly accurate, with meticulous attention to detail. Right first-time mentality Intermediate level of Technical competence in the interpretation and methodology required to interpret ISO 13485 requirements in relation to Class I and Class II medical devices Ability to work and communicate with others in a professional and effective manner, within a team-oriented environment. Show a mindset and behaviour appropriate to a quality ambassador for the company setting the best example to other employees and external regulators and customers Be intellectually curious and self-motivated to drive self-learning and utilise mentoring opportunities within the company Proactive mentality within the workplace to drive solutions orientated outcomes in collaboration with other team members Ability to work in collaborative and independent work situations Ability to remain calm and receptive in fast paced situations Having an open mind, ready to learn and improve Skills & experience Knowledge and/ or experience of both ISO 13485 & European medical device requirements (MDD 93/42/EEC and MDR (EU) 2017/745) is mandatory Knowledge of quality management systems and associated documentation Bachelor's degree or equivalent in a related field At least 2 years' experience working in a regulated medical device manufacturing environment Be aware of the latest medical device regulations and standards. Knowledge of Microsoft Office including Excel, with an ability and experience performing intermediate level data analysis About us Medicareplus International is part of the Chemilines Group of companies. It is a fast growing market innovator in the research, manufacture and distribution of cost effective, clinically proven protective and regenerative healthcare products that maintains skin integrity. We are located in Wembley, London and offer free onsite parking. The nearest Tube stations include, Alperton, Hanger Lane and Perivale (Piccadilly & Central Lines). What we offer SME company with plenty of opportunities to grow and shine. Competitive salary, immediate start. 23 days holiday plus statutory 8 bank holidays. Auto enrolment into pension scheme. Free car parking on site. Staff discount on certain products...... click apply for full job details

Scientific Editorial Lead London & Remote Working Up to £55k We are looking for a passionate leader with a huge love for the science of medicine. Are you looking to manage talented whilst driving creative solutions for clients briefs? Let's chat! Our client are a global medical communications agency with offices in London & USA. With a team of over 100 people who are all dedicated to the story of medicine, you will be joining a business where everyone shares the same global vision and are committed to doing the best work on behalf of clients. So, where do you come in? Well, we're glad you asked! If you love communicating medical science, t his is a key role within the team, which supports there current growth. You will take on responsibility for the end-to-end management of one or more therapy areas including immunology, cardiology and neurology. This opportunity would suit a senior scientific/medical writer or editor with an excellent track record in medical communications, medical education or healthcare advertising who would like to step up into a management position. This is also an attractive role for those already working as a manager who may wish to move to an agency where team members are given the chance to shape and influence communications accounts. This agency are enthusiastic to support each individual's growth and career ambitions, so we can guarantee this will be an agency that can take you to a new level. Some of the responsibilities include: · Managing a team of medical editors to ensure efficient delivery of high quality materials, incorporating regular performance and development review. · Coordination with account management team for messaging/compliance sign off. · Coordination of budgets and timelines with account management team. · Strategic content input during client interactions. · Representing the company at events and client meetings. · Managing resourcing and training requirements both within the team and, with the other Scientific Team Leaders, across teams. · Scheduling work with Creative and Digital teams. · Communicating effectively with all departments and senior management, and proactively seeking ways to improve efficiency or quality to achieve team goals. · Having in-depth understanding of several therapeutic areas, and offering scientific leadership and support for members of the content team. · Providing input to project proposals and attending pitches as required to secure new business and grow existing accounts. Experience we are looking for: · On-site and client-facing experience essential. · Life science degree essential. · Appropriate industry experience, ideally in an agency environment. · Experience of broad range of medical education activities across the full range of media. · Excellent editorial skills. · Strong Team management experience and dedicated to coaching and leading to get the best out the team. · Proven organisational and planning abilities. · Proactivity and problem-solving skills. · Excellent written and oral communication skills. P If this sounds like the role you've been waiting for, we would love to speak with you!..... click apply for full job details

PLEASE MENTION THE GREENJOBS NETWORK OF WEBSITES WHEN APPLYING TO THIS CAREER OPPORTUNITY Officer 1 (Environmental Data Collection Officer) • Location: Flexible within South West Wales • Grade & Salary: 4, £25,828 rising to £29,352 over four years • Post number: 202493 • Type of contract: Fixed term appointment until 31 March 2021 • Work pattern: Full time Closing date: 20 September 2020 Benefits: Civil Service pension, 28 days annual leave, rising to 33 days over 5 years, flexible working options, occupational health including counselling and advisory services and eye care, childcare vouchers and salary sacrifice schemes. Role Purpose We are looking for an enthusiastic individual to join our team as an Environmental Data Collection Officer for Southwest Wales. You would work as part of the SW Wales Environmental Assessment and Advice Team. We provide multifunctional advice and monitoring across SW Wales. This post will focus on delivery in the field across Neath Port-Talbot, Swansea, Carmarthenshire, Pembrokeshire and some work in Ceredigion. You will be confident about working outdoors in different field environments, weather conditions, and sometimes in remote locations, and you will be comfortable working in water to carry out data collection and survey work. This varied role, based in the field, includes: • Collect routine water quality samples in rivers, lakes and bathing waters. • Ecological kick-sampling to detect invertebrates and diatoms. • Terrestrial monitoring support. • Drive from site to site, including some routes when a 4x4 vehicle is required. • Use technology to collect data in the field with a hand held meter and input data on a tablet device. • Operating equipment such as data sondes and passive sampling equipment in a river. The data collected by our team are used to report against statutory requirements and are key evidence used by Place Teams in Wales, to inform their decisions and actions in the sustainable management of our natural resources. Qualifications and Skills • Experience of operational sampling and/or monitoring. • Experience of team working. • Reasonable knowledge of terrestrial ecology, freshwater ecology, water quality, fisheries or earth science. • Data and information management experience. A current full UK valid licence to drive NRW fleet vehicles (cars and vans). • Ability to swim and be confident working in water. (Essential) • IT competencies; MS Office and database experience. For more information, please visit our website.

PLEASE MENTION THE GREENJOBS NETWORK OF WEBSITES WHEN APPLYING TO THIS CAREER OPPORTUNITY Lead Specialist Advisor, Water & Brexit • Location: Flexible in Wales • Grade & Salary: 7 - £37,973 rising to £42,584 over three years • Post number: 202091 • Type of contract: Fixed term for two years • Work pattern: full time Closing date: 17 September 2020 Benefits: Civil Service pension, 28 days annual leave, rising to 33 days over 5 years, flexible working options, occupational health including counselling and advisory services and eye care, childcare vouchers and salary sacrifice schemes. Role Purpose With the diverse nature of NRW's remit this is an exciting opportunity to work in the Sustainable Water group within the Evidence, Policy and Permitting (EPP) Directorate. The location is flexible within Wales working as part of the Integrated Water Planning Team. The role will provide the expert lead on water and manage the preparation of NRW policy, programmes, plans, strategies and guidance developed in relation future policy and delivery mechanisms. This will translate Welsh & UK Government policy into practical approaches for delivery and an opportunity to help shape UK and Welsh legislation or the future for Water. The role will also support and lead on some aspects the wider work of the team including River Basin Management Planning, water related areas of work on Sustainable Management of Natural Resources and Water Company Planning. The post holder will work with colleagues from other teams in EPP and Operations, officials from WG and sector representatives. This is an opportunity to work in a diverse, professional and stimulating environment with the ability to opt into NRW Sports and Social events and with National Parks, scenery and culture on the doorstep. The role comes with a generous package including 28 days annual leave (rising to 33 days over 5 years), flexi-time scheme which allows you to work flexibly between 7am and 7pm, flexible working arrangements, a generous career-average pension scheme, eye care, tax free childcare schemes, corporate benefit schemes such as cycle-to-work and discounts at many retailers, plus occupational health, counselling and advisory services. Staff also have the ability to purchase additional annual leave up to 10 days (pro-rata). Qualifications and Skills • Knowledge of: Welsh, UK and EU legislation related to water management; Welsh & UK Governments & EU policy drivers in water resources, water quality; and the issues and opportunities in Wales; • Knowledge and practical understanding of the range of partners and stakeholders involved with water management in Wales; • Experience of: In-depth understanding of the water management discipline and the complex range of drivers and barriers to delivery; • Working in a programme and project management environment with Project Management experience and/or qualifications; • Representing the organisation in high profile and contentious issues in the public arena; • Share your knowledge and expertise to help solve problems, supporting all Heads of Business in EPP as required. For more information, please visit our website.

Ardmore Group is seeking for a Design Manager to join our team and contribute to the completion of our prestigious sites in Hammersmith. The senior Design Manager we are looking for must have HND'S or Architectural Technology Degree, Construction related Degree. architectural practice experience in multi story new builds, developer experience and dealt with building regulation application. We required to have a knowledge of ASTA Power Projects, MS Projects, AutoCAD, BREEAM, SMART Waste, Building Regulations (including Part B) and previously working on high end residential projects, hand-on, dynamic and keen to take every opportunity to fast-track your career. Key Areas of Responsibility Understand the clients brief, ER's, specification and drawings and as far as practicable ensure the project is built accordingly, assisting in the resolution of any ER discrepancies with the commercial team as they arise Set up with the Senior document controller the document control and information portals / systems with Document Controller Manage the document controller Prepare trackers to manage the full D&B build process using the pro-formas from the Intranet. Assist in the preparation of the Design Responsibility Matrix (DRM) Develop the Design Risk Assessment (DRA) and assist in the ongoing Technical Audits Produce the information release schedule (IRS) Building and MEP using ACL pro-forma docs and formally agree it with the Design Team Compile the Risk Register using the ACL pro forma with the assistance of the design and site team Assist in the development of the procurement schedule and be actively involved in the procurement process for all of the packages commencing with the Consultants Appointments Chair and manage design team meetings including production and issue of minutes in a timely manner Provide value engineering and buildability reviews with technical feedback to the project team Manage and track the design development process, using CDCP, RFI protocols, tech subs, etc. Understand the full requirements of the CSH and BREEAM and manage the process through our appointed consultants looking for best value design to economically meet code compliance to meet the timer constraints of the project Ensure that information release accords with agreed IRS Develop sub-contractors and Suppliers design/specs with the design team ensuring that full ER and Statutory compliance is met Co-ordinate drawings and check that the drawings comply with the ER's and Standards Ensure the issued information is to the correct standard and is fully detailed within 'For Construction Status' Be actively involved with the sampling process including the production of the samples sign off pro-forma Be actively involved with site QA particularly at the commencement of a new activity to ensure that we are building to and installing components and details as prescribed in the ER's. Make arrangements for the suppliers technical / QA staffs to be in attendance so they can sign off the control samples Use the ACL Project Completion Matrix to track the design and technical close out of the project Assist in the production and collation of the O & M manuals About Ardmore Group The Ardmore Group is one of the largest family owned construction companies in the UK. Although we have delivered across the UK, we are best known as London's builder given our unrivalled reputation for delivering large scale residential, hotel and regeneration schemes in London since our creation in 1974. Ardmore has been involved in hundreds of major projects across London, including landmark buildings that have shaped the face of the capital. We have established a major reputation for delivery of large-scale phased regeneration schemes. We were the first tier-one contractor at the Athlete's Village for the London Olympics and are lead contractor on two of London's largest regeneration programme in Lewisham and Greenwich. In addition to our expertise in the residential sector we have extensive experience in delivering bespoke luxury hotel refurbishment schemes. In 2011, we completed the luxurious Corinthia Hotel, and followed that success by delivering two of the best new hotels in the world in 2017 at the Four Seasons, Ten Trinity Square and the Ned at Poultry. "As part of our recruitment process for all roles including employees, consultants and subcontractors, we collect and process personal data relating to job candidates and potential candidates. We explain how we use personal information in the Candidate privacy notice". To view our Candidate privacy notice please visit the Ardmore Group website > Working for us > Candidate privacy notice. Ardmore are an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, gender, reassignment, religion or belief, marital status, or pregnancy or maternity. Unsolicited CVS: in relations to speculative CVs received form providers without a prior assignment issued in writing by Ardmore's Recruitment team, no fee payable by Ardmore will apply...... click apply for full job details

Data Analyst Location: Cheltenham Clearance: DV Rate: £475 to £515 per day (DOE) Our Client is looking for a DV Cleared Data Analyst to provide data analysis to support delivery of a client programme. Key Deliverables: Provide contextual alignment across MOD and NCSC finances and resource management such that we may correctly represent attribution relative to both. Preserving the ability to present single truth overall. Provide a bridge between the programme and the PCOs. Primarily using MS Excel, possibly some use of PowerBi in the longer term. Skills Required: Currently operating at SFIA level: 3-4 Experience of an area of consultancy (e.g...... click apply for full job details

Job Description Your potential plus our commitment changes lives National Care Group (NCG) is a leading provider of care and support services to vulnerable adults throughout the United Kingdom. We work closely with the people we support, their family members, local authorities and care providers to provide high quality, person-centred support to an ever-increasing number of people across the country. NCG specialise in supporting young individuals and adults with a wide range of disabilities and needs. We are proud to offer the following services: supported living, residential care, outreach & home support, and day services. We are looking for a Full Time Data Analyst to join our team in Daventry. The successful candidate will provide crucial support to the Quality team, and other departments when needed. As the person responsible for collecting and analyzing information relating to the quality of our services and the effectiveness of our support the successful candidate will play a key role in the 'continuous improvement' of our services. The primary focus of the role is the collection and recording of accurate and relevant information along with the timely presentation of that information in formats that are accessible and productive. Supporting the Quality team through the collection and analysis of information relevant to a set of organisational and operational targets. The development and management of appropriate databases will be an essential task as will be the provision of management reports. The successful candidate will be a subject matter expert in the use of our Governance System (Access Care Compliance) and our Health & Safety System (Citation). The role provides a mix of planned and reactive activity which the successful candidate will be expected to manage, developing process and practice based on their knowledge and experience. As one of the UK's leading providers of care and support services to vulnerable adults, National Care Group fully appreciate the amazing and life changing work our teams do. That is why we offer: A Competitive salary of £30,000 33 days holiday per year, including bank holidays. Specialist and Blended Training and Development - we believe in promoting from within Access to Digital Perks where you can gain discounts on gym memberships, shopping, theme parks, travel and more Rewards and recognition for your work Key Responsibilities: Oversee and quality manage the inputting of relevant data and information. Develop systems and strategies to collect, record and store information required for quality outcomes reporting. Support quality outcomes by planning, communicating effectively and collecting information from a range of sources, including interviews, questionnaires and incident reporting. Summarising these in agreed reporting formats on a regular and ad hoc basis. Ability to analyse and present information in such a way that it supports monitoring and planning needs. Provide Administration support to the Quality Team, including sending out stakeholder questionnaires, formatting reports etc. Work under the direction of the Quality Director and support the Commercial Director to present the results in a format for discussion and planning purposes at individual, team, and senior management levels. Support the PBS implementation process. Liaise closely with Executive colleagues to keep them apprised of any significant information that comes to light in relation to an individual. Work effectively with other professionals within NCG in order to help improve and develop their information systems. Be able to present findings in a range of settings, attend meetings and contribute to discussions. Continually develop and improve the processes to enhance the customer journey and development of Quality monitoring processes. Be familiar with and comply with all Company policies, procedures and legislative requirements governing the organisation and its services. Share expertise and learning with other members of the commercial and Quality Teams and the wider organisation. Work flexibly and support all regions to manage variable workloads and resource pressures To apply for this positions you must have: Experience in the data collection techniques and the analysis of data. Experience of setting up and maintaining databases for the purpose of providing accurate and relevant reports. Experience of assessing customer needs such as a triage process or sales environment. Training in the use of databases and Microsoft office software programmes. Ability to analyse and interpret information from a variety of sources, verbal, written and numerical. Able to form positive relationships and influence through effective communication with internal colleagues and external partners at all levels. Be computer literate and adept at presenting information in appropriate and readily accessible formats. Knowledge of GDPR and the handling of confidential information. Knowledge of the social care sector and the role and responsibilities of private sector care providers...... click apply for full job details

Role: Laboratory Analyst Duration: Ongoing - Full time Contract Successful candidates will have experience of the analysis of APIs, raw materials and excipients and the associated analytical techniques that may include chromatographic (HPLC, GC, IC), spectroscopic (IR, LC-MS, ICP-OES, Atomic Absorption), physical properties (particle size analysis) and/or pharmacopoeial testing. You must be highly proficient in the use of common laboratory instruments and software packages for the above analytical techniques. In addition, experienced in problem solving and have the expertise in troubleshooting both analytical equipment and methodology...... click apply for full job details