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        • witney, south east
        • contract
        • £30.00 - £50.00 per hour
        • randstad cpe
        Are you looking for a new role as a Senior Statistician? If you are interested in working for a leading Medical Device and Healthcare business this could be the role for you! The successful candidate will be supporting and providing direction to clinical studies and to the development of products and testing procedures. This will include Leading activities, liaising with customer groups, applying appropriate statistical methods and data analysis support to products and internal processes. The ideal candidate would be able to lead the statistical support for clinical studies aimed at demonstrating product efficacy and safety as well as provide supervision of other colleagues through performance reviews and development plans. This role is offered on a contract basis initially for 6 months, working full time Mon-Fri. Due to COVID-19 this role will be home based, however candidates will be expected to work on site when the guidelines change. Responsibilities: Involved in end-to-end clinical trials for a small number of global projects that typically last from 4 to 18 monthsSupporting protocol development to preparing publicationsYou will be providing key statistical support to the development of our clients pipeline productsContribute to, or manage, a small number of projects, and work with colleagues from a range of backgrounds to explain statistical concepts to them Requirements BSc in Mathematics or Statistics (or equivalent)SAS ExperienceAttention to detail is essentialMust have experience in using SAS, word processor applications, spreadsheets and databasesData analysis and report writingExperience in a highly regulated industry such as Medical Devices or Pharmaceutical Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
        Are you looking for a new role as a Senior Statistician? If you are interested in working for a leading Medical Device and Healthcare business this could be the role for you! The successful candidate will be supporting and providing direction to clinical studies and to the development of products and testing procedures. This will include Leading activities, liaising with customer groups, applying appropriate statistical methods and data analysis support to products and internal processes. The ideal candidate would be able to lead the statistical support for clinical studies aimed at demonstrating product efficacy and safety as well as provide supervision of other colleagues through performance reviews and development plans. This role is offered on a contract basis initially for 6 months, working full time Mon-Fri. Due to COVID-19 this role will be home based, however candidates will be expected to work on site when the guidelines change. Responsibilities: Involved in end-to-end clinical trials for a small number of global projects that typically last from 4 to 18 monthsSupporting protocol development to preparing publicationsYou will be providing key statistical support to the development of our clients pipeline productsContribute to, or manage, a small number of projects, and work with colleagues from a range of backgrounds to explain statistical concepts to them Requirements BSc in Mathematics or Statistics (or equivalent)SAS ExperienceAttention to detail is essentialMust have experience in using SAS, word processor applications, spreadsheets and databasesData analysis and report writingExperience in a highly regulated industry such as Medical Devices or Pharmaceutical Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
        • witney, south east
        • permanent
        • £40,000 - £50,000 per year
        • randstad cpe
        Are you looking for a new role within Health and Safety? Do you hold a NEBOSH diploma? If you are interested in working for a leading Medical Device and Healthcare business this could be the role for you! You will be responsible for identifying and managing project work, managing the site emergency response team, developing and conducting safety training, and consulting and communicating knowledge regarding Cal/OSHA, NFPA, DOT and EPA standards and regulations. This is a contract position, offered initially on a 6 month contract basis working 37.5 hours per week. Duties: The position is also responsible for communicating and implementing safety programs throughout the facility and assisting in the investigation of safety incidentsResponsible for implementing and maintaining the effectiveness of the quality systemCommunicate and implement any Corporate, Divisional, Federal, State and Local regulations and ensure compliance with these regulationsDevelop and implement EHS policies and programsDevelops and conducts EHS training and provides resources to assist in training employees on safe work practicesInterface with employees and departments on safety, transportation and environmental related issues and concernsAssist with site Emergency Response TeamInitiate and submit safety and environmental reports to management, Division, Corporate and regulatory agenciesInvestigate accidents and develop correctionsComplete EHS projects as assignedOverall site wide employee health and safety responsibilities and accountabilityAlso responsible for Domestic Field Sales EHS programsExperience / QUalifications: NEBOSH General Certificate which is essential to provide knowledge and understanding of EHS regulations, practices and policies or relevant vocational experienceExperience of EHS issues to ensure a competent response to EHS legal requirementsExperience of working within a manufacturing environment Computer literate, preferably with knowledge of software packages such as Word, Excel, Power point and VisioExcellent working knowledge of OSHA, EPA, DOT and NFPA regulatory standards requiredNice to haves: Bachelors Degree in Industrial Safety, other related disciplines or equivalentKnowledge of applicable regulatory standards and requirements for medical device industry ideal Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
        Are you looking for a new role within Health and Safety? Do you hold a NEBOSH diploma? If you are interested in working for a leading Medical Device and Healthcare business this could be the role for you! You will be responsible for identifying and managing project work, managing the site emergency response team, developing and conducting safety training, and consulting and communicating knowledge regarding Cal/OSHA, NFPA, DOT and EPA standards and regulations. This is a contract position, offered initially on a 6 month contract basis working 37.5 hours per week. Duties: The position is also responsible for communicating and implementing safety programs throughout the facility and assisting in the investigation of safety incidentsResponsible for implementing and maintaining the effectiveness of the quality systemCommunicate and implement any Corporate, Divisional, Federal, State and Local regulations and ensure compliance with these regulationsDevelop and implement EHS policies and programsDevelops and conducts EHS training and provides resources to assist in training employees on safe work practicesInterface with employees and departments on safety, transportation and environmental related issues and concernsAssist with site Emergency Response TeamInitiate and submit safety and environmental reports to management, Division, Corporate and regulatory agenciesInvestigate accidents and develop correctionsComplete EHS projects as assignedOverall site wide employee health and safety responsibilities and accountabilityAlso responsible for Domestic Field Sales EHS programsExperience / QUalifications: NEBOSH General Certificate which is essential to provide knowledge and understanding of EHS regulations, practices and policies or relevant vocational experienceExperience of EHS issues to ensure a competent response to EHS legal requirementsExperience of working within a manufacturing environment Computer literate, preferably with knowledge of software packages such as Word, Excel, Power point and VisioExcellent working knowledge of OSHA, EPA, DOT and NFPA regulatory standards requiredNice to haves: Bachelors Degree in Industrial Safety, other related disciplines or equivalentKnowledge of applicable regulatory standards and requirements for medical device industry ideal Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

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