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      • solihull, west midlands
      • work from home - contract
      • randstad inhouse services
      Randstad are looking for a Specialist Technical Support Technician to join their European team whilst working remotely. Pay Rate & Hours:Monday - Friday 8am - 4pmCompetitiveWorking wihtin a global heathcare leader's organisaztion you would be responsible for: * Provide technical support services in the field of Remote Patient Monitoring and CRM devices.* Provide technical information to customers in response to inquiries/report from the field.* Perform product evaluations and testing based on reports from the field.* Provide back-up support to Field Clinical Engineering/Sales Representatives in the areas of sales support (remote care and device management), regional training seminars and troubleshooting.* Provide and conduct product training to in-house personnel.* Assist in the presentation of educational material for new product training and in-service seminars to physicians, nurses and sales representatives.* Provides technical response to corporate website inquiries.* Coordinates efforts with international division staff to resolve product/clinical issues involvinginternational customers and the international sales issues. PLease apply if you feek this is the role for you.
      Randstad are looking for a Specialist Technical Support Technician to join their European team whilst working remotely. Pay Rate & Hours:Monday - Friday 8am - 4pmCompetitiveWorking wihtin a global heathcare leader's organisaztion you would be responsible for: * Provide technical support services in the field of Remote Patient Monitoring and CRM devices.* Provide technical information to customers in response to inquiries/report from the field.* Perform product evaluations and testing based on reports from the field.* Provide back-up support to Field Clinical Engineering/Sales Representatives in the areas of sales support (remote care and device management), regional training seminars and troubleshooting.* Provide and conduct product training to in-house personnel.* Assist in the presentation of educational material for new product training and in-service seminars to physicians, nurses and sales representatives.* Provides technical response to corporate website inquiries.* Coordinates efforts with international division staff to resolve product/clinical issues involvinginternational customers and the international sales issues. PLease apply if you feek this is the role for you.
      • tullamore, international
      • permanent
      • randstad financial services
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries.Company Profile:65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D.Responsibilities:* provide analytical competence and technology to Tullamore Site organisation so that all analytical methods are state-of-the-art and in compliance with regulatory expectations* to coordinate and control the day to day operations of the Quality Control laboratory including but not limited to providing a safe, secure and efficient working environment* ensuring all QC equipment is safely operated* all physical QC resources are maintained* stored and organised to allow efficient and effective operation* to control and direct all QC resources* operations and facilities in order to test all site materials from Raw Materials through to API* stability and utility samples and to manage and direct a QC team of skilled based individuals through sound personnel practices such as: - Performance management- Relevant and effective inductions- Identification of training needs- Coaching and Discipline* responsible for developing* monitoring* implementing, and reporting on the operating budget and staffing plan;- to monitor and report quality control progress- notifying any predicted shortfall or discrepancies against timescale and budgets.* immediate notification to the Site Quality Leader of any Quality Control issues and provide accurate and relevant information as required by the business* partner with the Quality Operations Lead to ensure alignment with planning and scheduling requirements, operational needs and implementation of OPEX and Drive continuous improvement initiatives which positively impact cycle time, productivity, efficiency and quality of work through Lean methodology* partner with QSS and Compliance Lead in support of implementation of Quality Systems and Inspection Readiness including internal and Health Authority Inspection* direct and oversee analytical services performed at Tullamore Site and third-party contract laboratories* oversee and direct the analytical method transfer for Tullamore Site products* ensure that analytical methods are adequately developed, validated, transferred and maintained* approve CMC documents related to analytical methods development & validations* develop and implement analytical method validation plans* ensure that adequate and timely analytical support for investigations (e.g. deviations, complaints) and troubleshooting is provided, where needed in conjunction with GMT, Opex, external 3rd party laboratories, and other involved functions to minimise the impact on product availability and sales* to continuously review quality control processes, procedures and capabilities in order to sustain the most cost-effective and efficient methods for meeting quality requirements* ensure the adequate and timely qualification of contract laboratories using appropriate quality management tools to monitor and ensure third party lab compliance with Quality Policies and applicable regulatory requirements on an ongoing basis e.g. QA Agreements, audits with appropriate follow up, risk assessments, Product Optimisation action plans, performance indicators, follow up stability and product quality review* actively manage the Quality Control Analytical team and set up their development and objective targets. They will mentor their team providing input and coaching on behaviors and professional development will provide timely feedback; and evaluate performance of direct reports after obtaining the relevant functional input and evaluation* review and monitor action plans for correction of audit observations related to the Analytical Labs and follow-up as appropriate.Education:* Bachelor of Science in Chemistry with +15 years of quality control and analytical laboratory experience and proven demonstrated experience in leading a QC team* Minimum of 5 years PROGRESSIVE experience in the quality control, quality assurance, manufacturing function of veterinary or human API products with prior roles at Manager Level in a Quality/Technical Manufacturing environment an essential prerequisite* Recognised Lean Six Sigma Qualification (Green Belt or Black belt)* Training & Experience at the application of Change Execution Methodology. Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries.Company Profile:65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D.Responsibilities:* provide analytical competence and technology to Tullamore Site organisation so that all analytical methods are state-of-the-art and in compliance with regulatory expectations* to coordinate and control the day to day operations of the Quality Control laboratory including but not limited to providing a safe, secure and efficient working environment* ensuring all QC equipment is safely operated* all physical QC resources are maintained* stored and organised to allow efficient and effective operation* to control and direct all QC resources* operations and facilities in order to test all site materials from Raw Materials through to API* stability and utility samples and to manage and direct a QC team of skilled based individuals through sound personnel practices such as: - Performance management- Relevant and effective inductions- Identification of training needs- Coaching and Discipline* responsible for developing* monitoring* implementing, and reporting on the operating budget and staffing plan;- to monitor and report quality control progress- notifying any predicted shortfall or discrepancies against timescale and budgets.* immediate notification to the Site Quality Leader of any Quality Control issues and provide accurate and relevant information as required by the business* partner with the Quality Operations Lead to ensure alignment with planning and scheduling requirements, operational needs and implementation of OPEX and Drive continuous improvement initiatives which positively impact cycle time, productivity, efficiency and quality of work through Lean methodology* partner with QSS and Compliance Lead in support of implementation of Quality Systems and Inspection Readiness including internal and Health Authority Inspection* direct and oversee analytical services performed at Tullamore Site and third-party contract laboratories* oversee and direct the analytical method transfer for Tullamore Site products* ensure that analytical methods are adequately developed, validated, transferred and maintained* approve CMC documents related to analytical methods development & validations* develop and implement analytical method validation plans* ensure that adequate and timely analytical support for investigations (e.g. deviations, complaints) and troubleshooting is provided, where needed in conjunction with GMT, Opex, external 3rd party laboratories, and other involved functions to minimise the impact on product availability and sales* to continuously review quality control processes, procedures and capabilities in order to sustain the most cost-effective and efficient methods for meeting quality requirements* ensure the adequate and timely qualification of contract laboratories using appropriate quality management tools to monitor and ensure third party lab compliance with Quality Policies and applicable regulatory requirements on an ongoing basis e.g. QA Agreements, audits with appropriate follow up, risk assessments, Product Optimisation action plans, performance indicators, follow up stability and product quality review* actively manage the Quality Control Analytical team and set up their development and objective targets. They will mentor their team providing input and coaching on behaviors and professional development will provide timely feedback; and evaluate performance of direct reports after obtaining the relevant functional input and evaluation* review and monitor action plans for correction of audit observations related to the Analytical Labs and follow-up as appropriate.Education:* Bachelor of Science in Chemistry with +15 years of quality control and analytical laboratory experience and proven demonstrated experience in leading a QC team* Minimum of 5 years PROGRESSIVE experience in the quality control, quality assurance, manufacturing function of veterinary or human API products with prior roles at Manager Level in a Quality/Technical Manufacturing environment an essential prerequisite* Recognised Lean Six Sigma Qualification (Green Belt or Black belt)* Training & Experience at the application of Change Execution Methodology. Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      • witney, south east
      • temp to perm
      • randstad inhouse services
      Product Returns InvestigatorDo you have excellent written communication skills? Are you computer literate? Are you comfortable working as an individual? We are looking for Product Return Investigators to join a global medical device and healthcare leader based in Witney.This role involves investigating why a product has been returned using in-house computer systems. You will be investigating the quality of returned products by finding the cause of their faults. Pay Rate: £10.26 per hourHours:Monday to FridayDays: 8 am - 4 pm (part time available)Benefits:Full training providedFree on-site parkingOnsite canteen and outside seating areasExcellent long term prospectsFriendly and welcoming teamModern on site facilitiesNewly expanded laboratory settingWeekly onsite Covid testing available for staff Responsibilities:Conduct investigations on customer returned products in accordance with site and divisional proceduresProactively support the implementation of new and / or improved processesCommunicate in a professional manner with colleagues worldwideMeet division goals for timeliness of complaint investigations and identify opportunities for improvement and/or better efficiencies in investigation processes.Conform to all relevant legislation and company Health and Safety policies.Pro-active in recommending improvements in terms of recommending cost savings through complaint process improvements and data quality, in line with Business Excellence initiatives.Keep up to date with the development of new products and through collaboration with peers within the complaints team and across the business, support activities required for complaint readiness prior to product launch. Identifying any trends in product complaints that are found during investigations and highlighting these to managementHandling multiple tasks effectively and efficiently in a team environment with minimal supervisionRequirements:Experience of using computer packages including Word and Excel.5 years of referencing (employment or alternative activity) history will need to be obtained if you are successful in your application.Candidates must be eligible to live and work in the UK.If this is a role you are interested in and you want to work for a renowned healthcare company, don't hesitate, apply today! Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      Product Returns InvestigatorDo you have excellent written communication skills? Are you computer literate? Are you comfortable working as an individual? We are looking for Product Return Investigators to join a global medical device and healthcare leader based in Witney.This role involves investigating why a product has been returned using in-house computer systems. You will be investigating the quality of returned products by finding the cause of their faults. Pay Rate: £10.26 per hourHours:Monday to FridayDays: 8 am - 4 pm (part time available)Benefits:Full training providedFree on-site parkingOnsite canteen and outside seating areasExcellent long term prospectsFriendly and welcoming teamModern on site facilitiesNewly expanded laboratory settingWeekly onsite Covid testing available for staff Responsibilities:Conduct investigations on customer returned products in accordance with site and divisional proceduresProactively support the implementation of new and / or improved processesCommunicate in a professional manner with colleagues worldwideMeet division goals for timeliness of complaint investigations and identify opportunities for improvement and/or better efficiencies in investigation processes.Conform to all relevant legislation and company Health and Safety policies.Pro-active in recommending improvements in terms of recommending cost savings through complaint process improvements and data quality, in line with Business Excellence initiatives.Keep up to date with the development of new products and through collaboration with peers within the complaints team and across the business, support activities required for complaint readiness prior to product launch. Identifying any trends in product complaints that are found during investigations and highlighting these to managementHandling multiple tasks effectively and efficiently in a team environment with minimal supervisionRequirements:Experience of using computer packages including Word and Excel.5 years of referencing (employment or alternative activity) history will need to be obtained if you are successful in your application.Candidates must be eligible to live and work in the UK.If this is a role you are interested in and you want to work for a renowned healthcare company, don't hesitate, apply today! Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      • witney, south east
      • temp to perm
      • randstad inhouse services
      Quality Inspector (Returned Products)Do you have excellent written communication skills? Are you computer literate? Are you comfortable working as an individual? We are looking for Product Return Investigators to join a global medical device and healthcare leader based in Witney.This role involves investigating why a product has been returned using in-house computer systems. You will be investigating the quality of returned products by finding the cause of their faults. Pay Rate: £10.26 per hourHours:Monday to FridayDays: 8 am - 4 pm (part time available)Benefits:Full training providedFree on-site parkingOnsite canteen and outside seating areasExcellent long term prospectsFriendly and welcoming teamModern on site facilitiesNewly expanded laboratory settingWeekly onsite Covid testing available for staff Responsibilities:Conduct investigations on customer returned products in accordance with site and divisional proceduresProactively support the implementation of new and / or improved processesCommunicate in a professional manner with colleagues worldwideMeet division goals for timeliness of complaint investigations and identify opportunities for improvement and/or better efficiencies in investigation processes.Conform to all relevant legislation and company Health and Safety policies.Pro-active in recommending improvements in terms of recommending cost savings through complaint process improvements and data quality, in line with Business Excellence initiatives.Keep up to date with the development of new products and through collaboration with peers within the complaints team and across the business, support activities required for complaint readiness prior to product launch. Identifying any trends in product complaints that are found during investigations and highlighting these to managementHandling multiple tasks effectively and efficiently in a team environment with minimal supervisionRequirements:Experience of using computer packages including Word and Excel.5 years of referencing (employment or alternative activity) history will need to be obtained if you are successful in your application. Candidates must be eligible to live and work in the UK.If this is a role you are interested in and you want to work for a renowned healthcare company, don't hesitate, apply today!Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      Quality Inspector (Returned Products)Do you have excellent written communication skills? Are you computer literate? Are you comfortable working as an individual? We are looking for Product Return Investigators to join a global medical device and healthcare leader based in Witney.This role involves investigating why a product has been returned using in-house computer systems. You will be investigating the quality of returned products by finding the cause of their faults. Pay Rate: £10.26 per hourHours:Monday to FridayDays: 8 am - 4 pm (part time available)Benefits:Full training providedFree on-site parkingOnsite canteen and outside seating areasExcellent long term prospectsFriendly and welcoming teamModern on site facilitiesNewly expanded laboratory settingWeekly onsite Covid testing available for staff Responsibilities:Conduct investigations on customer returned products in accordance with site and divisional proceduresProactively support the implementation of new and / or improved processesCommunicate in a professional manner with colleagues worldwideMeet division goals for timeliness of complaint investigations and identify opportunities for improvement and/or better efficiencies in investigation processes.Conform to all relevant legislation and company Health and Safety policies.Pro-active in recommending improvements in terms of recommending cost savings through complaint process improvements and data quality, in line with Business Excellence initiatives.Keep up to date with the development of new products and through collaboration with peers within the complaints team and across the business, support activities required for complaint readiness prior to product launch. Identifying any trends in product complaints that are found during investigations and highlighting these to managementHandling multiple tasks effectively and efficiently in a team environment with minimal supervisionRequirements:Experience of using computer packages including Word and Excel.5 years of referencing (employment or alternative activity) history will need to be obtained if you are successful in your application. Candidates must be eligible to live and work in the UK.If this is a role you are interested in and you want to work for a renowned healthcare company, don't hesitate, apply today!Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      • witney, south east
      • temporary
      • £12.50 per hour
      • randstad inhouse services
      Are you looking for a part time role a few days per week? Are you looking to support essential workers? If yes, we have a fantastic opportunity for you. On behalf of our client we are recruiting for a number of COVID-19 Rapid Test Operatives to support the implementation and delivery of the Rapid Covid-19 testing programme based on our client's site. Benefits You'll Love:Training and full personal protective equipment providedFree on-site parking Subsidised onsite canteen Outside seating areasPay Rate & Hours:Monday, Wednesday and Thursday: 17:30pm - 02:00am22.5 hours£12.50 per hourResponsibilities: Administer rapid throat and nasal swab tests on a daily basis Delivery of testing servicesReport on test results Following on site health and safety Requirements:Not be classified or live with anyone in the COVID-19 high risk groups Good interpersonal skills Data entry experience IT proficient Eligible to live and work in the UKOver 18 1 year of referencing (employment or alternative activity) Desirable:Experience in a medical, clinical or health setting If you tick all the boxes, then why not click apply today!
      Are you looking for a part time role a few days per week? Are you looking to support essential workers? If yes, we have a fantastic opportunity for you. On behalf of our client we are recruiting for a number of COVID-19 Rapid Test Operatives to support the implementation and delivery of the Rapid Covid-19 testing programme based on our client's site. Benefits You'll Love:Training and full personal protective equipment providedFree on-site parking Subsidised onsite canteen Outside seating areasPay Rate & Hours:Monday, Wednesday and Thursday: 17:30pm - 02:00am22.5 hours£12.50 per hourResponsibilities: Administer rapid throat and nasal swab tests on a daily basis Delivery of testing servicesReport on test results Following on site health and safety Requirements:Not be classified or live with anyone in the COVID-19 high risk groups Good interpersonal skills Data entry experience IT proficient Eligible to live and work in the UKOver 18 1 year of referencing (employment or alternative activity) Desirable:Experience in a medical, clinical or health setting If you tick all the boxes, then why not click apply today!

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