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        • port talbot, wales
        • contract
        • £30,000 - £38,000 per year
        • randstad cpe
        Sourcing Manager The opportunity on offerWe are looking to recruit a procurement professional who will maintain and develop supplier market knowledge. You will be responsible for regularly scanning the European and global marketplace and suppliers, collecting facts and then delivering relevant marketplace and supplier data, including 'clean sheet' analysis, to ensure effective construction of category strategies in close co-operation with key stakeholders for the best interest of Tata Steel UK. You will convert demands of TSUK end users and construct an effective business requirements overview, and an appropriate sourcing plan that maximises value across TSUK within the framework of an agreed category strategy. You will deliver all required aspects of pre-contract work, supplier selection, negotiation, closing and putting in place contracts that deliver short and medium term value for TSUK. Managing the contract through its life cycle by frequently analysing its effectiveness, in close co-operation with the contract management organisation and the end user and taking action based on KPI results.Applicants will also Operate as the point of leadership for vendor relationships ensuring fact-based communication as well as taking accountability for ensuring that operations-based contract managers are engaged in contract strategies, escalating effectively where performance gaps appear. Manage through "influence, gravitas and expertise" the effective delivery of value throughout the life of the contract.Who we're looking forYou will be an experienced Procurement/Purchasing professional educated to degree level in a technical or business related field, or equivalent practical experience. Applicants will have relevant experience in Commodity Management, Strategic Sourcing or Supply Chain Management experience.Ideally, you will have experience or be interested in developing cost models, cost trends and product development. We're looking for applicants who have the confidence in collaborating and working cross-functionally with operations/manufacturing teams, engineering, finance and legal.TSUK purchases items/services across a wide range of sectors/categories so particular experience in one or more areas of the following would be of particular interest to us:Procurement of Goods/servicesRaw materials used for steelmaking operations including category knowledge in metals, ferrous scrap, alloys, chemicals, industrial paint, refractories, minerals, packagingMarket AnalysisGlobal Sourcing The successful candidate will be able to operate within an cross functionally based team and be willing to travel as required.Our UK Procurement organisation has responsibility for the lowest possible cost base and maximizing the value out of supply agreements for Tata Steel; delivering a professional procurement service to businesses and leading several pan-Tata Steel procurement sectors; and also leading a stronger drive for supply chain effectiveness and realisation of challenging group and business-specific targets. 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.
        Sourcing Manager The opportunity on offerWe are looking to recruit a procurement professional who will maintain and develop supplier market knowledge. You will be responsible for regularly scanning the European and global marketplace and suppliers, collecting facts and then delivering relevant marketplace and supplier data, including 'clean sheet' analysis, to ensure effective construction of category strategies in close co-operation with key stakeholders for the best interest of Tata Steel UK. You will convert demands of TSUK end users and construct an effective business requirements overview, and an appropriate sourcing plan that maximises value across TSUK within the framework of an agreed category strategy. You will deliver all required aspects of pre-contract work, supplier selection, negotiation, closing and putting in place contracts that deliver short and medium term value for TSUK. Managing the contract through its life cycle by frequently analysing its effectiveness, in close co-operation with the contract management organisation and the end user and taking action based on KPI results.Applicants will also Operate as the point of leadership for vendor relationships ensuring fact-based communication as well as taking accountability for ensuring that operations-based contract managers are engaged in contract strategies, escalating effectively where performance gaps appear. Manage through "influence, gravitas and expertise" the effective delivery of value throughout the life of the contract.Who we're looking forYou will be an experienced Procurement/Purchasing professional educated to degree level in a technical or business related field, or equivalent practical experience. Applicants will have relevant experience in Commodity Management, Strategic Sourcing or Supply Chain Management experience.Ideally, you will have experience or be interested in developing cost models, cost trends and product development. We're looking for applicants who have the confidence in collaborating and working cross-functionally with operations/manufacturing teams, engineering, finance and legal.TSUK purchases items/services across a wide range of sectors/categories so particular experience in one or more areas of the following would be of particular interest to us:Procurement of Goods/servicesRaw materials used for steelmaking operations including category knowledge in metals, ferrous scrap, alloys, chemicals, industrial paint, refractories, minerals, packagingMarket AnalysisGlobal Sourcing The successful candidate will be able to operate within an cross functionally based team and be willing to travel as required.Our UK Procurement organisation has responsibility for the lowest possible cost base and maximizing the value out of supply agreements for Tata Steel; delivering a professional procurement service to businesses and leading several pan-Tata Steel procurement sectors; and also leading a stronger drive for supply chain effectiveness and realisation of challenging group and business-specific targets. 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.
        • fareham, south east
        • permanent
        • £35,000 - £40,000, per year, 33 days holiday
        • randstad cpe
        Manufacturing SupervsiorAre you an Manufacturing Supervsior who has been involved with a high level of Lean Manufacturing? Are you an Manufacturing Supervsior who is passionate about making a difference? Do you have the drive to make a difference? Are you looking for a new position to work within a manufacturing facility and have that type of experience? Do you have a great eye for detail? If so then this might be the job for you. We require an excellent Manufacturing Supervsior to join one of the UK's leading manufacturing businesses. This is on a permanent basis located in Hampshire.Main responsibilitiesDelivery of manufactured products from the immediate production processes in line with quality, cost, and delivery targets.Promotion and delivery of Lean, Continuous Improvement (CI) techniques and processes, and promote a culture of continuous improvement.Identify and lead improvements in their, and other, function's processes and ways of working.Deliver 'excellent' customer service to both internal and external customers.Develop, promote, and deliver 'On-time, in full' (OTIF) for customer requirements.Work in close collaboration with other business functions to ensure and promote quality and delivery performance.Any other duties commensurate with the grade and level of responsibility of this role, for which the holder has the necessary experience and/or training.Machine shop / machining / assembly experience 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.
        Manufacturing SupervsiorAre you an Manufacturing Supervsior who has been involved with a high level of Lean Manufacturing? Are you an Manufacturing Supervsior who is passionate about making a difference? Do you have the drive to make a difference? Are you looking for a new position to work within a manufacturing facility and have that type of experience? Do you have a great eye for detail? If so then this might be the job for you. We require an excellent Manufacturing Supervsior to join one of the UK's leading manufacturing businesses. This is on a permanent basis located in Hampshire.Main responsibilitiesDelivery of manufactured products from the immediate production processes in line with quality, cost, and delivery targets.Promotion and delivery of Lean, Continuous Improvement (CI) techniques and processes, and promote a culture of continuous improvement.Identify and lead improvements in their, and other, function's processes and ways of working.Deliver 'excellent' customer service to both internal and external customers.Develop, promote, and deliver 'On-time, in full' (OTIF) for customer requirements.Work in close collaboration with other business functions to ensure and promote quality and delivery performance.Any other duties commensurate with the grade and level of responsibility of this role, for which the holder has the necessary experience and/or training.Machine shop / machining / assembly experience 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.
        • milton keynes, south east
        • permanent
        • £25,000 - £40,000 per year
        • randstad cpe
        Are you looking for a new role as an Office Manager? Do you want to work for a family-owned company that has been designing, building and selling professional products and robotic assisted solutions for exercise and therapy? If so, this could be the role for you!This is a permanent, full time role based in Milton Keynes. We are looking for someone with an independent working style, a "can-do-attitude", who shows self-initiative and who is work solution-oriented. Someone who loves to organise and tackle a variety of challenges. A strong communicator that others can rely on. Responsibilities: Manage officeLead administrator who operationally supports various of the following tasksManage stockOptimize administrative processes and structures Maintain service systemManage personnel Handle customer or general enquiries Manage quotations and orders Support in planning sales routes etc.Support with customer acquisition Manage invoices to customer and from suppliersPrepare banking/payments Support with annual P&L planning, financial statement, accountingManage administrative documents Update social media Coordinate website update Organise shows Book adverts, check magazinesQualifications/ Experience:Commercial skills, professional experience in similar positions and/or completed commercial educationBasic experience in working with databases or CRM systems Basic knowledge of financial proceduresBasic marketing and sales knowledgeBasic MS Office knowledgeSome experience with accountingExperience in working for small or medium enterprisesExperience with QuickBooks, Sage Act!, DocuSign 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 an Office Manager? Do you want to work for a family-owned company that has been designing, building and selling professional products and robotic assisted solutions for exercise and therapy? If so, this could be the role for you!This is a permanent, full time role based in Milton Keynes. We are looking for someone with an independent working style, a "can-do-attitude", who shows self-initiative and who is work solution-oriented. Someone who loves to organise and tackle a variety of challenges. A strong communicator that others can rely on. Responsibilities: Manage officeLead administrator who operationally supports various of the following tasksManage stockOptimize administrative processes and structures Maintain service systemManage personnel Handle customer or general enquiries Manage quotations and orders Support in planning sales routes etc.Support with customer acquisition Manage invoices to customer and from suppliersPrepare banking/payments Support with annual P&L planning, financial statement, accountingManage administrative documents Update social media Coordinate website update Organise shows Book adverts, check magazinesQualifications/ Experience:Commercial skills, professional experience in similar positions and/or completed commercial educationBasic experience in working with databases or CRM systems Basic knowledge of financial proceduresBasic marketing and sales knowledgeBasic MS Office knowledgeSome experience with accountingExperience in working for small or medium enterprisesExperience with QuickBooks, Sage Act!, DocuSign 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.
        • peterborough, east of england
        • permanent
        • £60,000 - £70,000 per year
        • randstad cpe
        Are you looking for a new role as a Compliance Officer? Do you want to work for a specialist medical technology business that develops, manufactures, and supplies products and services to enable hospitals and healthcare facilities to reduce the risk of infection? If so, this could be the role for you! This is a permanent, full time role. You can be based at our clients site either in Peterborough, or King's Lynn. The Compliance Officer will report to the Quality and Compliance Manager and will be a key aid to the business. With the support of expert consultants and using your knowledge of the regulatory landscape, you will ensure products are developed, manufactured, and distributed according to required regulations and standards.Responsibilities: Ensuring current products meet regulatory and technical standards, producing a top-level matrix of products and applicable regulatory requirementsSupport teams to develop PRD (Product Requirement Document) for new/future productsDemonstrate compliance with global regulationsPrepare data to obtain certifications and commercialisation authorisationsCompilation and submission of dossiers and ensuring suitability of product labelling and advertising for all products types in international marketsPrepare safety data sheetsTrack and report on assigned projectsManage relevant technical and compliance documentation and filesMaintain an awareness and ensure compliance with relevant regulations and laws in all marketsRegister products under country-specific requirementsAct as the regulatory representative in product development teamsReview current internal processesIdentify the need for any regulatory activitiesAttend audits by both internal and external bodies and conduct internal auditsPrepare regulatory documentation and dossiers for submissionWork closely with the team ensuring all set tasks meet the objectives and are scheduled appropriatelyProduce reports for management reviewWhere required, support Quality & Compliance team on all management systemsAdhere to all systems and procedures that the Company has instituted to meet statutory requirements and Inivos Policy on Health, Safety, Environment.Experience / Qualifications: Always represent our Core Values: Excellence, Resourceful, Innovation, Understanding and IntegrityStrong knowledge of scientific, regulatory, and business issuesPrevious experience of ensuring regulatory compliance, with a regulatory backgroundKnowledge and experience of European, US and Asian MarketsKnowledge of Regulatory frameworks (i.e., BPR, MDR, FDA, CE marking, UKCA)Experience in International Standards (i.e., 9001, 14001, 45001, 27001, 13485 & 14971)Knowledge of IEC 60601 series (desirable)Knowledge of design control, software lifecycle and risk management processes (desirable)Experience registering products (desirable)Experience with approval processes (desirable)Ability to work collaborativelyEnthusiastic and motivated to work in a fast-paced environmentExcellent IT SkillsHighly organised individual with a methodical working styleStrong verbal and written communication skillsConfidentiality in processing sensitive data 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 Compliance Officer? Do you want to work for a specialist medical technology business that develops, manufactures, and supplies products and services to enable hospitals and healthcare facilities to reduce the risk of infection? If so, this could be the role for you! This is a permanent, full time role. You can be based at our clients site either in Peterborough, or King's Lynn. The Compliance Officer will report to the Quality and Compliance Manager and will be a key aid to the business. With the support of expert consultants and using your knowledge of the regulatory landscape, you will ensure products are developed, manufactured, and distributed according to required regulations and standards.Responsibilities: Ensuring current products meet regulatory and technical standards, producing a top-level matrix of products and applicable regulatory requirementsSupport teams to develop PRD (Product Requirement Document) for new/future productsDemonstrate compliance with global regulationsPrepare data to obtain certifications and commercialisation authorisationsCompilation and submission of dossiers and ensuring suitability of product labelling and advertising for all products types in international marketsPrepare safety data sheetsTrack and report on assigned projectsManage relevant technical and compliance documentation and filesMaintain an awareness and ensure compliance with relevant regulations and laws in all marketsRegister products under country-specific requirementsAct as the regulatory representative in product development teamsReview current internal processesIdentify the need for any regulatory activitiesAttend audits by both internal and external bodies and conduct internal auditsPrepare regulatory documentation and dossiers for submissionWork closely with the team ensuring all set tasks meet the objectives and are scheduled appropriatelyProduce reports for management reviewWhere required, support Quality & Compliance team on all management systemsAdhere to all systems and procedures that the Company has instituted to meet statutory requirements and Inivos Policy on Health, Safety, Environment.Experience / Qualifications: Always represent our Core Values: Excellence, Resourceful, Innovation, Understanding and IntegrityStrong knowledge of scientific, regulatory, and business issuesPrevious experience of ensuring regulatory compliance, with a regulatory backgroundKnowledge and experience of European, US and Asian MarketsKnowledge of Regulatory frameworks (i.e., BPR, MDR, FDA, CE marking, UKCA)Experience in International Standards (i.e., 9001, 14001, 45001, 27001, 13485 & 14971)Knowledge of IEC 60601 series (desirable)Knowledge of design control, software lifecycle and risk management processes (desirable)Experience registering products (desirable)Experience with approval processes (desirable)Ability to work collaborativelyEnthusiastic and motivated to work in a fast-paced environmentExcellent IT SkillsHighly organised individual with a methodical working styleStrong verbal and written communication skillsConfidentiality in processing sensitive data 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.
        • peterborough, east of england
        • permanent
        • £60,000 - £70,000 per year
        • randstad cpe
        Are you looking for a new role as a Regulatory Affairs Specialist? Do you want to work for a specialist medical technology business that develops, manufactures, and supplies products and services to enable hospitals and healthcare facilities to reduce the risk of infection? If so, this could be the role for you! This is a permanent, full time role. You can be based at our clients site either in Peterborough, or King's Lynn. The Regulatory Affairs Specialist will report to the Quality and Compliance Manager and will be a key aid to the business. As a Regulatory Affairs Specialist you will use your knowledge of the regulatory landscape to ensure products are developed, manufactured, and distributed according to required regulations and standards.Responsibilities: Maintain product compliance matrix document tracking compliance changes and requirementsLiaise with external parties Ensure products meet regulatory and technical standardsShare knowledge of regulationsDemonstrate compliance with global regulationsPrepare data to obtain certifications and commercialisation authorisationsCompilation and submission of dossiers and ensuring suitability of product labelling and advertising for all products types in international marketsPrepare safety data sheetsTrack/report on assigned projectsManage relevant technical documentation and filesMaintain an awareness and ensure compliance with relevant regulations and laws in all marketsRegister products under country-specific requirementsAct as the regulatory representative in product development teamsReview processes and procedures Identify the need for any regulatory activitiesAttend audits Prepare regulatory documentation and dossiers for submissionWork closely with the team ensuring all set tasks meet the objectives and are scheduled appropriately. Ensure compliance records are kept up to date.Experience / Qualifications:Always represent our Core Values: Excellence, Resourceful, Innovation, Understanding and IntegrityStrong knowledge of scientific, regulatory, and business issuesExperience with a BPR/MDR background (cosmetic may be considered) 3+ years' experience in a similar role is essential Knowledge of European, US and Asian markets is essential Knowledge and awareness of the relevant regulatory guidelines and legislationPrevious experience of ensuring compliance with MDR and BPRRelevant Bachelor's degreeExcellent knowledge of regulatory frameworks (BPR, MDR, FDA, CE marking, UKCA)Experience in International Standards (ISO 13485 & 14971)Knowledge of IEC 60601 seriesKnowledge of design control, software lifecycle and risk management processesExperience registering biocidal products and medical devicesExperience with biocidal and medical device approval processesAbility to work collaborativelyEnthusiastic and motivated to work in a fast-paced environmentStrong communication skills both oral and writtenOrganisational skills & developing regulatory project management skills 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 Regulatory Affairs Specialist? Do you want to work for a specialist medical technology business that develops, manufactures, and supplies products and services to enable hospitals and healthcare facilities to reduce the risk of infection? If so, this could be the role for you! This is a permanent, full time role. You can be based at our clients site either in Peterborough, or King's Lynn. The Regulatory Affairs Specialist will report to the Quality and Compliance Manager and will be a key aid to the business. As a Regulatory Affairs Specialist you will use your knowledge of the regulatory landscape to ensure products are developed, manufactured, and distributed according to required regulations and standards.Responsibilities: Maintain product compliance matrix document tracking compliance changes and requirementsLiaise with external parties Ensure products meet regulatory and technical standardsShare knowledge of regulationsDemonstrate compliance with global regulationsPrepare data to obtain certifications and commercialisation authorisationsCompilation and submission of dossiers and ensuring suitability of product labelling and advertising for all products types in international marketsPrepare safety data sheetsTrack/report on assigned projectsManage relevant technical documentation and filesMaintain an awareness and ensure compliance with relevant regulations and laws in all marketsRegister products under country-specific requirementsAct as the regulatory representative in product development teamsReview processes and procedures Identify the need for any regulatory activitiesAttend audits Prepare regulatory documentation and dossiers for submissionWork closely with the team ensuring all set tasks meet the objectives and are scheduled appropriately. Ensure compliance records are kept up to date.Experience / Qualifications:Always represent our Core Values: Excellence, Resourceful, Innovation, Understanding and IntegrityStrong knowledge of scientific, regulatory, and business issuesExperience with a BPR/MDR background (cosmetic may be considered) 3+ years' experience in a similar role is essential Knowledge of European, US and Asian markets is essential Knowledge and awareness of the relevant regulatory guidelines and legislationPrevious experience of ensuring compliance with MDR and BPRRelevant Bachelor's degreeExcellent knowledge of regulatory frameworks (BPR, MDR, FDA, CE marking, UKCA)Experience in International Standards (ISO 13485 & 14971)Knowledge of IEC 60601 seriesKnowledge of design control, software lifecycle and risk management processesExperience registering biocidal products and medical devicesExperience with biocidal and medical device approval processesAbility to work collaborativelyEnthusiastic and motivated to work in a fast-paced environmentStrong communication skills both oral and writtenOrganisational skills & developing regulatory project management skills 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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