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Eurofins
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  • Junior IT Infrastructure Engineer  

    - Wolverhampton
    Job DescriptionWorking hours are Monday - Friday, 9am - 5pm.Please not... Read More
    Job DescriptionWorking hours are Monday - Friday, 9am - 5pm.Please note, this role will require regular travel across our Eurofins UK & Ireland sites.As a Junior IT Infrastructure Engineer, you will provide IT Infrastructure support and delivery services to users and supported sites across the United Kingdom and Ireland, as part of a single, cross-border IT Infrastructure team.This role supports the delivery of end user computer services and associated infrastructure, working under the guidance of more experienced engineers and in collaboration with the wider IT Infrastructure team and specialist regional or global teams as required.The role provides an opportunity to build practical experience across the IT Infrastructure function, with progression of responsibility aligned to capability, experience and individual aspiration.Main DutiesProvide desk-side and remote IT support to users, diagnosing and resolving hardware, software and connectivity issues that fall within the post holder’s skills and experience.Provide basic local support for IT Infrastructure services and equipment, including end user devices, servers, VoIP telephony and network infrastructure, within defined scope and under supervision.Log, manage and progress Incidents and Service Requests.Raise Incidents, Requests or Change Requests for other teams or engineers.Install, configure and support end user devices and associated equipment (including PCs, laptops and peripherals).Support routine end user computer activities such as device builds, rebuilds and deployments.Support the management of end user device assets, including receiving, staging, issuing, tracking and decommissioning equipment.Create and maintain technical, operational and site documentation.QualificationsITIL Foundation or equivalent certificationRelevant Microsoft or endpoint-related certificationPrevious experience in an IT support or technical role, or demonstrable practical aptitude for ITExposure to structured IT service processes (incident, request or change)Experience working as part of a team in a professional or technical environmentWillingness to learnAdditional InformationBenefitsAt Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events, and we are committed to charitable causes through global fundraising activities.As a Eurofins employee you will benefit from:Enhanced Annual Leave EntitlementCompany Pension PlanLife Assurance Scheme (4 times annual salary)Enhanced Maternity, Adoption and Paternity SchemesEmployee Assistance Programme – 24/7 confidentialHealth Cash PlanHealth and Wellbeing ProgrammesFree parkingWorldwide career opportunitiesWe also have in place rewards recognising the great work out employees deliver, their dedicated service and celebrating special life events.What Happens NextOur people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths. 
    Your data 
    As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.
     
    Closing Date
    We reserve the right to close or extend this position depending on application numbers. Therefore we would urge candidates to submit an application as early as possible.

    Due to the high volume of applications we receive please be aware that if you do not receive a response within 4 weeks of the vacancy expiry date unfortunately, on this occasion your application has been unsuccessful. We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Read Less
  • Product Compliance Specialist – Household Cleaners/ Detergents  

    - Northampton
    Job DescriptionThe Role:The Product Compliance Specialist will play a... Read More
    Job DescriptionThe Role:The Product Compliance Specialist will play a key role within our Retail Solution Centre in ensuring that all retailer products, their packaging, labelling, artwork and documentations meet applicable regulatory, environmental, and quality standards. The product approval process will follow the critical path to product launch. Supporting our clients and their suppliers, the Specialist will work cross-functionally to ensure that all aspects of the product comply with relevant requirements, providing expert guidance and technical support.Main duties: Responsible for a variety of products within our client’s Hardline and Softline product ranges.Ensuring compliance of product to specific regulatory and retail requirements.Product approval process – responsible for meeting Critical Path deadlines through the approval process to launch.Review and approve technical specifications and relevant documents.Review and approve product artwork, packaging, and labelling to ensure compliance with regional and product specific regulatory and retail requirements.Communication to external stakeholders including technical and regulatory guidance, critical path deadlines, product and documentation non-compliances and supplier monitoring.Ensure products are legally compliant and fit for purpose.Maintain product status on the critical path and keep detailed accurate records of all communications in an orderly fashion.Working with Product Lifecycle Management (PLM) software for all products critical path and document control.Build positive and effective relationships with Quality Assurance, Buying teams and suppliers.Attend retailer meetings as and when required either face to face or virtually using teams.Any other reasonable task requested to support the business.QualificationsWhat We Are Looking For:Experienced in a similar regulatory role ideally within Quality, retailer or supply chain environment Proven experience working within the UK and EU regulatory frameworks including General Product Safety Regulation.Experience reviewing and approving packaging, labelling, artwork and product documentations for compliance.Proven experience and understanding of product sealing procedures.Understanding of critical path management and working with retailers, brands, buying and sourcing offices, vendors, suppliers, and factories.Understanding manufacturing processes and production experience in the product areas.Demonstrates a self-motivated, resilient and above all positive approach to working with all stakeholders.Highly organised, detail-orientated, and comfortable managing multiple projects and stakeholders.Excellent written and verbal communication skills with the ability to interpret complex regulations and translate into actionable business requirements.Team spirit is essential and must be a pro-active, organised and resilient individual who thrives in a fast-paced environment with a “can-do” attitude.Delivering quality in all our work is key, so accuracy, speed and attention to detail is essential whilst meeting given priorities/ deadlines.Additional InformationBenefits:Office based role - 37.5 hours - Monday to Friday, Competitive Salary, Life Assurance 4 x salary, Private Medical Insurance, Healthcash Care Plan, Income Protection, Group Pension Scheme (match contribution of up to 5 %), Option to buy up to 5 days holiday a year, Perkbox (access to discounts), Employee Assistance Programme – 24/7 confidential support, World-wide career opportunities.Hybrid working will be considered, you must be able to attend the office in Northampton upto 2 days a week if required. Read Less
  • Research Manager - (Food, drink and personal care)  

    - Reading
    Job DescriptionReporting to an Associate Research Director or a Resear... Read More
    Job DescriptionReporting to an Associate Research Director or a Research Director, a Research Manager is the primary contact for client communication before/during/after projects and owns and delivers full research projects.Responsibilities:1. Client Management: a. Can be a Key Account Manager (KAM) for 1 or a few clients b. Direct contact for communication before, during and after projects delivery2. Project Management:a. Autonomous management, implementation and coordination of complex research projects b. Taking clients briefs and writing study proposals c. Propose appropriate methodologies and research approaches d. Prepare estimates for ad hoc studies e. Contribute in negotiating contracts, or specifications, technically, methodologically and financially f. Ensure that projects meet objectives and are delivered on-time and within budget g. Ensure that the project work meets agreed quality standards h. Report writing with storytelling i. Presentation of results, including relevant recommendations j. Moderation of some expert panel sessions for training and evaluation purposes  k. Responsible of panel performance: analysis, recommendations, and action plan execution3. Strategy: Ensuring that ongoing activities and projects adhere to the company's strategic guidelines4. Revenue: Share feedback with managers on clients needs & potential revenue risks5. People: a. Close collaboration with the Data Solutions Hub (our in-house data analysis team) b. Work closely with other members of our sensory and research teams and the fieldwork teamQualificationsMinimum 3 years of industry experience in market research and/or sensory researchKnowledge of food and/or personal care / OTC pharma products, quantitative and qualitative consumer research methodologies, sensory methodologies and statisticsExcellent written and oral communication skills in EnglishProficiency in MS Office: Word, Excel, PowerPoint, etcRigorous, responsive and proactiveStrong organisational and planning skills, that ensure work is effectively prioritised to meet deadlinesAdditional Information Read Less
  • Pharmaceutical Packaging Technician  

    - Liverpool
    Job DescriptionUnfortunately, we are unable to offer visa sponsorship... Read More
    Job DescriptionUnfortunately, we are unable to offer visa sponsorship for this role.This is a fulltime, permanent position working 35 hours per week either of the below Shift Patterns:Shift Pattern 1: Monday – Thursday 07:00 – 15:00 & Friday 07:00 – 12:00.
    Shift Pattern 2: Monday – Thursday 08:30 – 16:45 & Friday 08:30 – 12:30. This scope of work involves supporting the Clinical Supplies Operation (CSO) Packaging team. The individual executing this scope of work will work in close collaboration with the following: Quality and EHS as required.Job Responsibilities:Competent experience of start-up, operate and close down primary, secondary and clinical kits production operations in accordance with appropriate SOPs.Collaborating with client contacts and working with support and to ensure room and equipment cleanliness, material receipt and control, label and product accountability confirmation, automation set-up and correct functioning, conduct in-process tests and post-operation equipment strip down and clean.Competent experience constructing clinical trial kits in accordance with strict protocols to maintain blinding integrity.Able to independently control and monitor production processes and equipment; resolve problems or correct abnormal conditions, conduct basic troubleshooting and escalate problems appropriately.Participate in equipment validation and system user acceptance testing as required.Complete electronic batch documentation, equipment log books and other documentation relevant to the production process for all stages of production for both product and labels.Fluent working knowledge of relevant electronic system operations, including SAP, temperature monitoring and product stability information systems.Competent understanding in following the clients GMP related quality standards of relevant packaging, label authoring, printing, inspecting and logistics environments.Fluent understanding in the internal and external regulatory environment pertinent to clinical trials and pharmaceutical development and support internal audits and regulatory inspections.Competent understanding in blinding principles and conduct in-process controls to maintain blinding integrity.Liaise with Quality groups to ensure appropriate approvals and chain of custody.Document data as dictated by current Client policies and procedures.Ensure that the client gets the best possible service by continually reviewing best practice in relation to both commercial and quality issues and ensuring 100% ethical work standards.Be aware of the client’s requirements and strive to meet or exceed those requirements keeping in mind the client process end points.Deal with client queries and contact designated personnel, with appropriate support from onsite leadership with minimal support.To ensure that the client’s requirements are fully met or exceeded and in so doing will be flexible to work in any area of the business as is required.Document data as dictated by current Client policies and procedures.Fluent with and keep up to date with any client based processes and regulatory changes, ensuring their training is complete and adjusting their work as required with approval from the Lead Scientist or client.To revise SOPs as required by the Lead Scientist or Client contact.QualificationsPrevious experience of working in a Packaging Technician role within a regulated pharmaceutical environment.Relevant experience in a packaging pharmaceutical experience.Competent experience of constructing clinical trial kits and maintaining blinding integrity.Fluent understanding of regulatory processes associated with conducting clinical trials.Experienced working in line with GMP with a competent understanding of the processes and documentation that maintain the license to operate.Competently navigate and work using fully electronic media, including MS Office and SAP.Good communication skills, both written and verbally clearly presents information to build understanding which helps to form strong working relationships with colleagues.Good team player, organised, accurate, have strong documentation skills.Good communication skills both internally and externally and avoids making mistakes that will hinder the understanding of written and verbal exchanges.Passionate about quality and customerAdditional InformationAt Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events, and we are committed to charitable causes through global fundraising activities.As a Eurofins employee you will benefit from:Reward and RecognitionHealth Cash PlanLife Assurance (4 times annual salary).Company Pension PlanEmployee Assistance Programme – 24/7 confidential support.Free car parkingWorldwide career opportunitiesEveryone who joins our team also gets access to Perkbox, allowing you to save money all year round. Whether its supermarket savings or days out, the daily coffee or a summer holiday – there’s something to suit everyone’s lifestyle.What Happens NextOur people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths. 

    Your data 
    As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.

    We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Read Less
  • Research Manager - (Food, drink and personal care)  

    - Crawley
    Job DescriptionJob DescriptionReporting to an Associate Research Direc... Read More
    Job DescriptionJob DescriptionReporting to an Associate Research Director or a Research Director, a Research Manager is the primary contact for client communication before/during/after projects and owns and delivers full research projects.Responsibilities:1. Client Management: a. Can be a Key Account Manager (KAM) for 1 or a few clients b. Direct contact for communication before, during and after projects delivery2. Project Management:a. Autonomous management, implementation and coordination of complex research projects b. Taking clients briefs and writing study proposals c. Propose appropriate methodologies and research approaches d. Prepare estimates for ad hoc studies e. Contribute in negotiating contracts, or specifications, technically, methodologically and financially f. Ensure that projects meet objectives and are delivered on-time and within budget g. Ensure that the project work meets agreed quality standards h. Report writing with storytelling i. Presentation of results, including relevant recommendations j. Moderation of some expert panel sessions for training and evaluation purposes  k. Responsible of panel performance: analysis, recommendations, and action plan execution3. Strategy: Ensuring that ongoing activities and projects adhere to the company's strategic guidelines4. Revenue: Share feedback with managers on clients needs & potential revenue risks5. People:a. Close collaboration with the Data Solutions Hub (our in-house data analysis team)b. Work closely with other members of our sensory and research teams and the fieldwork teamQualificationsMinimum 3 years of industry experience in market research and/or sensory researchKnowledge of food and/or personal care / OTC pharma products, quantitative and qualitative consumer research methodologies, sensory methodologies and statisticsExcellent written and oral communication skills in EnglishProficiency in MS Office: Word, Excel, PowerPoint, etcRigorous, responsive and proactiveStrong organisational and planning skills, that ensure work is effectively prioritised to meet deadlinesAdditional Information Read Less
  • Analytical Product Development Scientist  

    - Macclesfield
    Job DescriptionThis is a fulltime, 12 Month Fixed Term position, worki... Read More
    Job DescriptionThis is a fulltime, 12 Month Fixed Term position, working a flexible 36.5 hour week, Monday – Friday.The purpose of this job is to support analysis of pharmaceutical Oral Drug Products and New Modalities with accurate results within an acceptable timeframe.Job Responsibilities:To perform routine and non-routine analysis using traditional and modern analytical techniques, as required by the Lead Scientist or customer representative.To review analytical data for GMP compliance.In line with experience support development and validation of analytical procedures used for Oral Drug Products and New Modalities like peptides.To prepare and approve results for tests in which they have received the appropriate training and are deemed competent.To train as required, other Eurofins or client employees in analytical techniques and electronic system in which the Analyst is competent.To initiate and follow-up OOS results and action limits as per customer procedures.To identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement.To document data as dictated by current client policies and procedures.To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards.To update any relevant documentation when requested by Lead Scientist or client representative.To participate in the preparation of reports.QualificationsA degree in Chemistry or a related discipline is required.Proven relevant experience of pharmaceutical analysis in a development laboratory, or equivalent, is desired.Experienced and competent with traditional analytical techniques as well as modern instrumental equipment (HPLC, Karl Fischer, Dissolution, Mass Spectroscopy and other Spectroscopic techniques). Able to interpret raw data and draw conclusions regarding troubleshooting of instruments and methods.Thorough understanding of chromatographic techniques with some trouble shooting capabilities.Thorough understanding of requirements for working in a GMP environment.Ability to quickly learn new processes. Works proactively to offer suggestions for new ways to improve existing processes.Additional InformationAt Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events, and we are committed to charitable causes through global fundraising activities.As a Eurofins employee you will benefit from:Reward and RecognitionHealth Cash PlanLife Assurance (4 times annual salary).Company Pension PlanEmployee Assistance Programme – 24/7 confidential support.Free car parkingWorldwide career opportunitiesEveryone who joins our team also gets access to Perkbox, allowing you to save money all year round. Whether its supermarket savings or days out, the daily coffee or a summer holiday – there’s something to suit everyone’s lifestyle.What Happens NextOur people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths. 
     
    Your data 
    As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.

    We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Read Less
  • Casework Support Officer  

    - Tamworth
    Job DescriptionWe are recruiting for a Casework Support Officer (CSO)... Read More
    Job DescriptionWe are recruiting for a Casework Support Officer (CSO) to join our team in Tamworth. This role is ideal for someone seeking a rewarding career in forensic testing within a well‑established, market‑leading organisation with over 30 years’ experience supporting Police Forces across England and Wales, as well as commercial and public sector clients.As a CSO, you will support Caseworking Scientists by handling exhibits, managing case receipt and return processes, and ensuring accurate documentation within our Laboratory Information Management System (C‑LIMS). You will play a key role in maintaining exhibit integrity, meeting customer requirements, and supporting smooth case progression.Key Responsibilities and AccountabilitiesReceive and return exhibits, following all processes to maintain integrity and continuity.Record and update case information in C‑LIMS.Triage and assess incoming cases, identifying key requirements and delivery deadlines.Package items for return and ensure all continuity records are completed.Carry out case administration including invoicing, pagination, filing, customer communication, defence requests and travel arrangements.Undertake general office duties such as managing post and escorting visitors.Adhere to Standard Operating Procedures, Customer Operational Protocols, Health & Safety, and the Eurofins Quality Management System.Communicate effectively with scientists and other team members throughout the case lifecycle.Maintain high standards of quality and customer service in a busy environment.QualificationsMinimum of 5 GCSE’s at grade 4-9 or above to include English, Maths and Science.Knowledge and experience of Microsoft and Google packages (Word, Excel, PowerPoint, Google Workspace)Understanding of the confidential nature of the businessExcellent written and oral communication skillsAbility to adapt quickly in a fast-paced, challenging environmentPreferred Knowledge, Experience and Technical SkillsPrevious experience of working in a support roleRecent experience of working within an environment handling forensic exhibitsBehavioursDemonstrate ownership of issues that arise day to day.Display patience, determination, attention to detail and integrity at all timesExhibit high levels of concentration, accuracy and reliability.Strong communication skills and the ability to work co-operatively with others, focussing on a collective goals.Excellent telephone manner and a focus on customer service.Demonstrate initiative, adopting a pro-active attitude to continuous improvement.Additional InformationDue to the highly sensitive nature of the work, applicants should note that security clearance is required for this role. To gain security clearance you must have five years continuous residency in the UK. Security clearance is undertaken by a third party to police personnel vetting standards (NPPV3 and SC), as such any criminal convictions (including criminal convictions held by: you, your partner, parents, siblings, children (over the age of 10) and anyone living with you (who doesn’t fit these relationships) may prevent you from gaining security clearance. Further information on the security clearance process and requirement can be found at . In addition, all successful applicants will be required to undertake drug and alcohol testing prior to commencing employment.In return for your hard work and loyal service, we will offer you a competitive salary, and a selection of employee benefits via our flexible benefits menu which includes cycle to work, give as you earn, volunteering days, buy and sell holiday. In addition, we also offer the following:Life Assurance (3 times annual salary)Scottish Widows Company Pension Plan25 days annual leave plus bank holidays (increasing to a maximum of 30 days)Employee length of service awards and yearly recognition schemes, celebrating work anniversaries here at EFS.Employee tech schemeDiscount vouchers and flexi reward points on our employee wellness hubEveryone who joins EFS will have access to Perkbox allowing you to save money all year round on a wide range of perks such as supermarket savings, days out or your daily coffeeLearning and study supportEmployee Assistance ProgrammeHealth Cash Plan membershipEnhanced company sick, maternity and paternity pay schemeRefer a friend schemeSubscription to mental health support and wellbeingFree on-site car parkingDue to the nature of the work we undertake on-site, you must inform us if you come into contact with any firearms or ammunition through work or any other reason as there will be precautions you will need to take in order to enter the premises. This also applies to persons involved in clay pigeon shooting, and those who regularly use any cartridge based tools such as nail/stud guns. Please provide details on your application. Read Less
  • Analytical Chemist  

    - Northampton
    Job DescriptionThe Role:Undertake the analysis of materials used in co... Read More
    Job DescriptionThe Role:Undertake the analysis of materials used in consumer products inclusive of (but limited to) leathers, textiles, polymers, metal hardware, jewellery, etc., for a wide range of restricted substances at low concentrations, according to international test methods. This will involve using various solvent extraction and matrix clean-up procedures, to prepare the test samples, followed by their analysis using advanced analytical laboratory instrumentation. Main Duties:Preparing liquid extracts from the samples using standardised solvent extraction and solid-phase extraction (SPE) clean-up procedures.Identifying and quantifying the specific restricted substances in the sample extracts using advanced analytical instrumentation such as, gas chromatography with mass spectroscopy and electron capture (GC-MS and GC-ECD), liquid chromatography (HPLC, LC-MS, LC-DAD), ion chromatography (IC), Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and UV-visible spectrophotometry.Processing the raw analytical data and maintaining analytical quality control charts.Maintaining instrumentation and a clean and tidy laboratory.Support the quality team within the laboratory functions, to maintain and add to the laboratory’s ISO 17025 accreditation including (but not limited) to: method validation, calibrations, controlled document reviews etc.Support sample preparation as needed with the deconstruction of product into individual components as well as accurately weighing and labelling for traceability, to enable testing to commence.Performing any other reasonable duties to assist the analytical testing team and the business.QualificationsWhat We Are Looking For:Degree educated in Chemistry or a related scientific discipline.Proven experience in inorganic chemistry and ICP-MS is desirable. Practical experience in the operation, maintenance and troubleshooting of analytical equipment including but not limited to: ICP-MS, GC-MS, HPLC, etc.Accountability and responsibility. Ability to communicate appropriately and effectively with colleagues.Positive can-do attitude with a sense of urgency, in a fast-paced environment reflecting the high sample volume of this market-leading commercial laboratory.Good attention to detail.Adherence to the highest quality standards of precision, accuracy, and record keeping for maintaining our UKAS accreditation for a wide range of methods.Ability to use initiative, multi-task and plan work effectively to meet strict deadlines.Good working knowledge of Microsoft Office software and Laboratory Information Management Systems (LIMS).A flexible approach to working additional hours when required.Additional InformationBenefits:Office based role - 37.5 hours - Monday to Friday, Competitive Salary, Life Assurance 4 x salary, Private Medical Insurance, Healthcash Care Plan, Income Protection, Group Pension Scheme (match contribution of up to 5 %), Option to buy up to 5 days holiday a year, Perkbox (access to discounts), Employee Assistance Programme – 24/7 confidential support, World-wide career opportunities. Read Less
  • Business Developer - Calibration  

    - Bideford
    Job DescriptionQualificationsAdditional Information
    Job DescriptionQualificationsAdditional Information Read Less
  • Sample Collector/Phlebotomist  

    - Sunderland
    Job DescriptionWe have a vacancy for a Sample Collector / Phlebotomist... Read More
    Job DescriptionWe have a vacancy for a Sample Collector / Phlebotomist to join our Sample Collections team within the Sunderland and surrounding areas, on an AD HOC/casual basis. Candidates must be professionally qualified Phlebotomists, have recent experience in various venepuncture techniques (predominately vacutainer and butterfly) and be able to collect samples in non-clinical settings. Hours: Zero hours – as and when required (AD-HOC). No evenings or weekends. The Role: Attending pre booked appointments at various locations in and around the Sunderland area - appointments can be up to a 2 hour radius from your home. Provide a professional hair, blood and DNA sample collection service. Maintain and develop excellent relationships with clients, donors as the public face of Lextox. Implement the requirements of the company Quality management System and help maintain ISO17025 accreditation. Ensure that all collections are undertaken in a safe, healthy and low risk environment and manner. Provide statements of truth at point of collection. QualificationsWhat we’re looking for: Excellent interpersonal and language skills. Full UK Driving Licence and MUST have own access to a vehicle with business insurance. A minimum of 2 years’ experience in Phlebotomy, post qualification (proof of Phlebotomy competency may be required). Desirable: Experience in working within the NHS / Blood Service. Experience in collecting hair and DNA samples (in-house training is provided for this aspect of the role). Additional InformationAssignments will generally be within a 2-hour radius of a collector’s home address by car. Access to your own vehicle is essential. Successful applicants will be paid on a per collection basis only, plus appropriate travel expenses will be paid, including fuel, parking fees and sample postage. Collections assignments will generally be at either a solicitor’s office, local authority office or donor’s home; appropriate PPE will be provided. For this position, the role will involve the taking of blood samples, where Hepatitis B vaccination is required. An enhanced DBS check will be an essential requirement for this role. Please note that we reserve the right to close any adverts once we have received a sufficient number of applications. If you decide to apply for this post but do not hear back from us within two weeks of your application, please assume that you have not been short-listed on this occasion. Lextox is a committed equal opportunities employer and does not unlawfully discriminate on the basis of any status or condition protected by applicable UK employment law.  Read Less

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