EHS Administrator - £25 per PAYE - East Lancashire - 3 months (extension likely) - Hybrid working (1-day WFH, 4 days onsite) Sector: Manufacturing / Chemical Yolk Recruitment is recruiting for a EHS Administrator to work with a global leader in the manufacturing and scientific research sector. This is an exciting opportunity to support the EHS monitoring programs at the clients cutting edge site. You will maintain site EHS, security and quality management systems and provide an EHS administration and support service to the site as a part of the EHS department. Responsibilities: Provide an EHS administrative and support service to the EHS department Support site EHS monitoring, and encourage a positive and proactive EHS culture Support the EHS team in the delivery of education, training, development and communication to all required site personnel to enhance EHS awareness Advise and assist managers and their teams to comply with the companies and site EHS, safety and quality policies, systems and legislation. Assist where required the programme to develop Standard Operating and Standard Engineering procedures (SOPs and SEPs), and on-going document management Liaise with and organise external providers such as occupational health, emissions monitoring and equipment calibration companies. Core Skills: EHS experience working in hazardous, chemical, pharmaceutical or equivalent manufacturing industry. Desirable Skills: Knowledge and experience of working with integrated management systems and ISO 9001, 14001 & 45001. Knowledge of EHS legislation including occupational health, environmental monitoring, permitting and waste management EHS Qualification - NEBOSH Certificate (or equivalent)
Apr 15, 2024
Full time
EHS Administrator - £25 per PAYE - East Lancashire - 3 months (extension likely) - Hybrid working (1-day WFH, 4 days onsite) Sector: Manufacturing / Chemical Yolk Recruitment is recruiting for a EHS Administrator to work with a global leader in the manufacturing and scientific research sector. This is an exciting opportunity to support the EHS monitoring programs at the clients cutting edge site. You will maintain site EHS, security and quality management systems and provide an EHS administration and support service to the site as a part of the EHS department. Responsibilities: Provide an EHS administrative and support service to the EHS department Support site EHS monitoring, and encourage a positive and proactive EHS culture Support the EHS team in the delivery of education, training, development and communication to all required site personnel to enhance EHS awareness Advise and assist managers and their teams to comply with the companies and site EHS, safety and quality policies, systems and legislation. Assist where required the programme to develop Standard Operating and Standard Engineering procedures (SOPs and SEPs), and on-going document management Liaise with and organise external providers such as occupational health, emissions monitoring and equipment calibration companies. Core Skills: EHS experience working in hazardous, chemical, pharmaceutical or equivalent manufacturing industry. Desirable Skills: Knowledge and experience of working with integrated management systems and ISO 9001, 14001 & 45001. Knowledge of EHS legislation including occupational health, environmental monitoring, permitting and waste management EHS Qualification - NEBOSH Certificate (or equivalent)
Computer Systems Administrator Harwell Science and Innovation Campus, Oxfordshire Salary £ 33,963 to £39,955 per annum, dependent upon skills and experience Full time / Flexible hours considered. Reference: 10553 About Us Diamond Light Source is one of the most advanced scientific facilities in the world. It houses the UK's synchrotron light source, producing beams of light 10 billion times brighter than the sun, to probe the structure and composition of matter. From viruses and vaccines, to alternative energy solutions and nanotechnology, it underpins research and innovation for more than 8000 scientists. The Diamond Scientific Computing Group provides an extensive computing infrastructure that supports Scientists in their efforts to capture experimental information, process and visualise terabytes of multidimensional data on the fly, and apply complex mathematical, fitting or theoretical models to interpret their results. About the Role An opportunity has arisen in the Scientific Computing team for a talented engineer to help push back the frontiers of science. The team designs, commissions and maintains all of the infrastructure required to enable the operation of the machine, data collection, data analysis and archival. This ranges from high performance computing hardware, through virtualisation and containerised solutions to cloud computing on and off premises. We are looking for someone who will engage with our scientists and engineers to make best use of modern development and deployment practices and provide best of breed solutions and support. The technical landscape changes at a relentless pace providing opportunities for an innovative engineer to improve performance, resilience and quality of infrastructure. Diamond Light Source is working towards a huge upgrade project that will see the entire synchrotron replaced with a state of the art machine in 2026. This will provide new challenges and opportunities to help drive the cutting edge of scientific research. Working within a close-knit and highly skilled group, you will collaborate and have the opportunity to support and develop other team members, and to create new projects. Your experience and underlying knowledge will permeate throughout the wider team, leading initiatives and inspiring others. You will have special responsibility to manage the computing requirements of the Diamond controls engineers. Through collaborating with similar facilities, you will help us to incorporate new methods, technologies and ways of working. You will help us adopt best practice in terms of security, and will contribute to the long term future of Diamond Light Source as a world leading scientific research facility. About You You will hold a degree in a STEM subject or demonstrate significant equivalent experience. You will have experience in developing and deploying production grade infrastructure. Exposure to configuration management and DevOps tooling is desirable. You will be a keen and tenacious problem solver who is prepared to work with subject matter experts to solve complex issues. You will display good interpersonal, communication and presentational skills to interact effectively with staff at all levels. Benefits Diamond offers an exceptional benefits package to support staff in achieving a positive work/life balance. This includes 25 days annual leave plus 13 days of statutory and company holidays, along with flexible working hours and an excellent pension scheme. Staff also have access to a range of amenities on site including a nursery, cafes, a restaurant and sports and leisure facilities. A relocation allowance may also be available where applicable. To Apply Please use the online application process to apply and tell us why you believe you are suitable for this role. The closing date for applications is 26 th September 2021.
Sep 13, 2021
Full time
Computer Systems Administrator Harwell Science and Innovation Campus, Oxfordshire Salary £ 33,963 to £39,955 per annum, dependent upon skills and experience Full time / Flexible hours considered. Reference: 10553 About Us Diamond Light Source is one of the most advanced scientific facilities in the world. It houses the UK's synchrotron light source, producing beams of light 10 billion times brighter than the sun, to probe the structure and composition of matter. From viruses and vaccines, to alternative energy solutions and nanotechnology, it underpins research and innovation for more than 8000 scientists. The Diamond Scientific Computing Group provides an extensive computing infrastructure that supports Scientists in their efforts to capture experimental information, process and visualise terabytes of multidimensional data on the fly, and apply complex mathematical, fitting or theoretical models to interpret their results. About the Role An opportunity has arisen in the Scientific Computing team for a talented engineer to help push back the frontiers of science. The team designs, commissions and maintains all of the infrastructure required to enable the operation of the machine, data collection, data analysis and archival. This ranges from high performance computing hardware, through virtualisation and containerised solutions to cloud computing on and off premises. We are looking for someone who will engage with our scientists and engineers to make best use of modern development and deployment practices and provide best of breed solutions and support. The technical landscape changes at a relentless pace providing opportunities for an innovative engineer to improve performance, resilience and quality of infrastructure. Diamond Light Source is working towards a huge upgrade project that will see the entire synchrotron replaced with a state of the art machine in 2026. This will provide new challenges and opportunities to help drive the cutting edge of scientific research. Working within a close-knit and highly skilled group, you will collaborate and have the opportunity to support and develop other team members, and to create new projects. Your experience and underlying knowledge will permeate throughout the wider team, leading initiatives and inspiring others. You will have special responsibility to manage the computing requirements of the Diamond controls engineers. Through collaborating with similar facilities, you will help us to incorporate new methods, technologies and ways of working. You will help us adopt best practice in terms of security, and will contribute to the long term future of Diamond Light Source as a world leading scientific research facility. About You You will hold a degree in a STEM subject or demonstrate significant equivalent experience. You will have experience in developing and deploying production grade infrastructure. Exposure to configuration management and DevOps tooling is desirable. You will be a keen and tenacious problem solver who is prepared to work with subject matter experts to solve complex issues. You will display good interpersonal, communication and presentational skills to interact effectively with staff at all levels. Benefits Diamond offers an exceptional benefits package to support staff in achieving a positive work/life balance. This includes 25 days annual leave plus 13 days of statutory and company holidays, along with flexible working hours and an excellent pension scheme. Staff also have access to a range of amenities on site including a nursery, cafes, a restaurant and sports and leisure facilities. A relocation allowance may also be available where applicable. To Apply Please use the online application process to apply and tell us why you believe you are suitable for this role. The closing date for applications is 26 th September 2021.
Johnson & Johnson is recruiting for a Clinical Administrator to join the team, located in Leeds for a contract of 12 months starting 30th November 2020.As an Administrator you will provide support to the clinical study staff within the Medical Device Group, as well as fostering strong, productive relationships with colleagues within the Medical Device Group organization.You will be responsible for processing, tracking, and filing of study documents, and management of the Trial Master File within the clinical projects. In addition, administratively support clinical study staff as required.You will also support project managers within the assigned clinical studies. Key ResponsibilitiesClinical Administration Tasks - (includes CTMS build and tracking, v-TMF build & upload).Under general supervision, accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions.Creation/distribution of regulatory binders & the wet-ink signed documents binder.Assist study staff and investigators to quickly and effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File). Respond to problems and assists in implementing corrective and preventive actions.Assist in providing internal communication of important clinical data and events.Support ongoing use of CTMS by maintaining and tracking relevant activities.Provide safety documentation to other functional groups in support of safety committee meetings as requested (supporting role).Other Administrative TasksMay be asked to provide support for study supplies creation, ordering and distribution to the sites e.g. print protocols, burn DVDs.May be asked to assist with Device tracking and ordering if required and if applicable.Assistance with logistics for Investigator meetings/expert panel meetings.Assistance with distribution of newsletter (create mailing list from CTMS and routing for internal approval).Participates in process improvement activities related to CTMS/v-TMF within the department.QualificationsEducationMinimum of a Bachelor's Degree is required.ExperiencePrevious clinical research experience is a plus.Requires previous administrative support experience or equivalent for at least 1 year.Clinical/medical background is a plus.KnowledgeRequires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point). Addition RequirementsDemonstrated competencies in the following areas are required:TrackingWritten and verbal communicationsAttention to detailsOrganizational skillsHaving similar clinical admin experience is a plus! If you think this role is for you please apply now!Our vision is to be the outstanding Health & Wellness organization by leveraging the commercial strategy to deliver competitive advantage and value creation for the consumer, customer and J&J. And as part of one of the largest and most diverse healthcare companies in the world, our brands leverage the company's world-class research tools and scientific prowess to provide consumers across the globe with innovative consumer medicines, skin, baby and crucial health solutions. We seek to meet the health needs of families everywhere through a broad range of well-known and trusted health products. At Johnson & Johnson we have a truly unrivalled brand portfolio with power brands across multiple categories including but not limited to Johnson's®, Neutrogena®, Nicorette®, Clean & Clear®, Listerine®, Calpol®, and Sudafed.
Nov 16, 2020
Full time
Johnson & Johnson is recruiting for a Clinical Administrator to join the team, located in Leeds for a contract of 12 months starting 30th November 2020.As an Administrator you will provide support to the clinical study staff within the Medical Device Group, as well as fostering strong, productive relationships with colleagues within the Medical Device Group organization.You will be responsible for processing, tracking, and filing of study documents, and management of the Trial Master File within the clinical projects. In addition, administratively support clinical study staff as required.You will also support project managers within the assigned clinical studies. Key ResponsibilitiesClinical Administration Tasks - (includes CTMS build and tracking, v-TMF build & upload).Under general supervision, accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions.Creation/distribution of regulatory binders & the wet-ink signed documents binder.Assist study staff and investigators to quickly and effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File). Respond to problems and assists in implementing corrective and preventive actions.Assist in providing internal communication of important clinical data and events.Support ongoing use of CTMS by maintaining and tracking relevant activities.Provide safety documentation to other functional groups in support of safety committee meetings as requested (supporting role).Other Administrative TasksMay be asked to provide support for study supplies creation, ordering and distribution to the sites e.g. print protocols, burn DVDs.May be asked to assist with Device tracking and ordering if required and if applicable.Assistance with logistics for Investigator meetings/expert panel meetings.Assistance with distribution of newsletter (create mailing list from CTMS and routing for internal approval).Participates in process improvement activities related to CTMS/v-TMF within the department.QualificationsEducationMinimum of a Bachelor's Degree is required.ExperiencePrevious clinical research experience is a plus.Requires previous administrative support experience or equivalent for at least 1 year.Clinical/medical background is a plus.KnowledgeRequires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point). Addition RequirementsDemonstrated competencies in the following areas are required:TrackingWritten and verbal communicationsAttention to detailsOrganizational skillsHaving similar clinical admin experience is a plus! If you think this role is for you please apply now!Our vision is to be the outstanding Health & Wellness organization by leveraging the commercial strategy to deliver competitive advantage and value creation for the consumer, customer and J&J. And as part of one of the largest and most diverse healthcare companies in the world, our brands leverage the company's world-class research tools and scientific prowess to provide consumers across the globe with innovative consumer medicines, skin, baby and crucial health solutions. We seek to meet the health needs of families everywhere through a broad range of well-known and trusted health products. At Johnson & Johnson we have a truly unrivalled brand portfolio with power brands across multiple categories including but not limited to Johnson's®, Neutrogena®, Nicorette®, Clean & Clear®, Listerine®, Calpol®, and Sudafed.