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We have several vacancies at different levels for R&D Scientists. We encourage applications from candidates with all levels of relevant experience in this field and will match candidates accordingly to roles based on experience. The job description below is an example of a mid-level role – other roles are available requiring less or more experience. We focus on the disposable component of diagnostic devices and have significant expertise with point of care (POC) in vitro diagnostic (IVD) tests. Our in-house capabilities range from screen printing and laser ablation of electrodes for biosensors to final device assembly, including the formulation and deposition of chemistries. Our modern facility is based in Livingston, central Scotland, less than 20 minutes from Edinburgh airport and 40 minutes from Glasgow. Further growth means that we are expanding our premises, capabilities, and systems. With a mixture of UK and international clients, we are a forward-looking organisation with an exciting future. As a qualified scientist you will bring hands‑on, technical expertise to the company. Having gained experience in the laboratory, you will understand in‑vitro diagnostics and may have some specific experience in electrochemical and other common assay detection methods. With an interest in how products work chemically, mechanically, and electrically it is probable that your work experience goes beyond the lab. As a contract business, we work on multiple projects simultaneously. This brings a lot of variety and requires people who are both willing and able to develop new products and processes in unison with our design control process. Your time will be spent working on some of our customer‑specific contracts (developing and manufacturing diagnostic products on their behalf) and working on internal development programmes. Working for a scale‑up organisation will provide you with a fantastic opportunity to make your mark and implement your ideas. Reporting to the Technical Lead/CSO, you will: – • Design and build reagents / formulate customer solutions to their requirements., • Develop and execute electrochemical methods for external customer requirements, and internal development programmes., • Develop reagent deposition methods and sensor build processes, to ensure rapid, consistent, and precise sensor production for development programmes., • Work with clients to devise and execute experimental designs (DoE’s) and create summary reports for discussion., • Author, oversee and execute protocols and write reports., • Develop product and process technical documents to successfully introduce new products and processes into manufacturing., • Communicate effectively with sub‑contractors, suppliers, and clients., • Provide scientific input into product and process designs ensuring optimal performance and client satisfaction., • Produce characterisation reports for customer products and development reports for projects, aligned with FMS design Quality Management System., • Stay informed of latest developments and trends in your field e.g. current trends and methods in IVD development through routine review of current scientific literature., • As a minimum, you will hold a degree level qualification in a relevant scientific subject., • You will have demonstrable, relevant experience gained in a regulated environment. However, consideration will be given where relevant academic experience can be demonstrated in lieu of industry experience., • Competent using routine and complex laboratory equipment., • Experienced in designing and building reagents and formulations from first principles., • Significant experience in electrochemical methods or other test measurement systems., • Experience of designing experimentation to resolve technical uncertainty through scientific rigor and root cause analysis., • Experience in IVD product development and familiar with Design Control concept., • Able to perform statistical analysis on data to drive decision making., • Understand Good Manufacturing and Good Laboratory Practices (GxP)., • Experience of working to ISO13485 and / or 21 CFR Part 820, and familiar with product and process validation., • A Green/Black Belt qualification in Six Sigma / process excellence is highly advantageous., • Competent in the use of modern manufacturing equipment (e.g. lasers, dispensing, lamination assembly)., • Understand Design for Manufacture (DFM) methodology., • Experienced using statistical tools such as Minitab and understand Design of Experiments methodology., • Experienced in reagent chemistry as applied in IVD products., • Experienced in surface chemistry: modification and analysis., • Experience in microfluidic devices., • People management experience would be advantageous. FlexMedical Solutions is a young and evolving start‑up organisation, now scaling, and operating in a highly regulated industry. The company is enjoying growth through success and is working on a number of leading edge projects with exciting customers. It is a changing environment that requires you to be very flexible and willing to learn and grow with the company. It is essential that you communicate with your team and contribute to the company’s success. As a provider of sub‑contract services, working for FlexMedical Solutions will bring a lot of variety and excitement; initiative will be rewarded, and personal development is a given. Please send your CV and a covering letter, outlining your suitability for the post: #J-18808-Ljbffr

IQVIA Laboratories seeks an Inventory Control Associate in Livingston, UK. This full-time role offers office-based and hybrid options, coordinating materials flow to and from storage and lab stock to ensure accuracy and efficiency. Responsibilities include receiving deliveries, logging, QC, stocking, distribution, and liaising with Purchasing/Finance on stock issues, with a focus on tidy shelves and proper rotation. #J-18808-Ljbffr

IQVIA Laboratories – Central Laboratory Service seeks an Associate Manager to supervise lab staff, set daily operational activities, and mentor team performance under management. The role emphasizes safety, quality, and cross-functional collaboration to drive efficient lab delivery. You will review metrics, implement process improvements, and ensure adherence to CAPA and quality systems while contributing to policy development and staff development in a global central laboratory setting. #J-18808-Ljbffr

Flexmedical Solutions, based in Livingston, is seeking an R&D Scientist to apply technical expertise in developing innovative diagnostic products. This role is crucial as we work on various customer-specific projects in a regulated environment. Candidates should have a degree in a scientific field and relevant lab experience. Responsibilities include reagent design, executing electrochemical methods, and ensuring compliance with quality systems. Join us and contribute your ideas in an evolving start-up that values growth and initiative. #J-18808-Ljbffr

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. We’re proud to be an armed forces-friendly place to work and welcome applications from reservists, armed forces veterans (including the wounded, injured and sick), as well as cadet instructors, and military spouses and partners. Unfortunately we are unable to offer sponsorship for this role. This is a part time position working 24 hours per week. Thursday, Friday 11:00-19:30 Saturday 08:30-17:00. • To prepare samples for incubation as per your trained areas., • To assist in the preparation of microbiological culture media and record the necessary Quality Control and Performance checks., • To carry out other functions in support of the Food Microbiology department., • To work to Eurofins Linlithgow’s Quality System showing due care and diligence in all activities., • To provide general assistance to Laboratory Staff at all levels., • To carry out housekeeping duties in line with Cleaning Schedules and other documents as required (including cleaning of equipment, floors, bins and benches when required), • To carry out all washroom duties as required being mindful of the glassware requirements., • To dispose of all laboratory waste in accordance with procedures., • To report any unsafe or poor working practices in the laboratory., • Ability to work alone or as part of a team., • Knowledge of the routine workings of a Lab Environment and the importance of a clean lab., • Verbal and written communication skills., • Computer literate, ability to use Word and Excel to basic level. At 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 Entitlement, • Annual Leave Sellback Scheme, • Additional Annual Leave at Employees set service dates, • Company Pension Plan, • Life Assurance Scheme (4 times annual salary), • Healthcare Cash Plan (6+ months service), • Enhanced Maternity, Adoption and Paternity Schemes, • Employee Assistance Programme – 24/7 confidential, • Health and Wellbeing Programmes, • Worldwide career opportunities, • We also have in place rewards recognising the great work our employees deliver, their dedicated service and celebrating special life events. Our 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. 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 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. 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. 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! Find out more in our career page: #J-18808-Ljbffr

We are a comprehensive global central laboratory services supporting clinical trials in countries around the world. Meeting the demands of today’s drug, device and diagnostics development environment requires a next generation service provider. IQVIA Laboratories helps sponsors enable laboratory testing in global clinical trials by providing specimen collection kits, a courier network, a biorepository, plus project management and data management. With extensive scientific expertise and industry leading capabilities in lab services, biomarkers, companion diagnostics, esoteric testing, high quality data and analytics, as well as global logistics and biorepository & specimen management, IQVIA Laboratories helps biotech and pharmaceutical companies meet their development needs. Responsible for supervising a team of lab staff and ensuring effective operational delivery and for setting day to day operational activities for the team with a focus on daily delivery. Under the mentorship of management, responsible for hiring, training, and performance management of staff. Supervises the daily activities of assigned laboratory work group(s) through appropriate delegation, technical skills training, and work supervision. Meets regularly with staff and senior management to discuss and resolve workload and technical issues. Responsible for ensuring activity in the team meets safety guidelines. Drives individual accountability for safety across the team. Identifies opportunities for improvements in safety. Responsible for the review of laboratory metrics to identify initiatives as well as establish additional metrics such as cost savings that are associated with process improvement initiatives. Ensures policies, practices and procedures are understood and followed by direct reports, customers and stakeholders. Ensures timely and appropriate resolution of CAPA and quality incidents, quality and compliance metrics, root cause analysis and improvement. Assists in establishment and revision of laboratory policies and procedures. Maintains appropriate control and quality assurance procedures. Ensures compliance with safety requirements. • Bachelor’s degree in a Human Biology based science., • 4 years of relevant experience in a clinical laboratory or clinical trials environment. (Immunology based), • Experience in technical leadership and cross-functional collaboration, • Proficiency with LIMS and other laboratory data systems., • Familiarity with CAPA processes and quality systems, • Ability to analyse and interpret complex data., • Ability to effectively coordinate and execute multiple tasks or projects simultaneously., • Ability to effectively write scientific and technical documents, • Understanding of LEAN 6 Sigma principles, • Global exposure, • Variety of therapeutic areas, • Collaborative and supportive team environment, • Access to cutting-edge and innovative, in-house technology, • Excellent career development and progression opportunities, • Work-Life Balance, with a strong focus on a positive well-being. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. #J-18808-Ljbffr

Sanctuary Personnel is seeking a Band 6 Biomedical Scientist specialising in Microbiology for a locum role in Livingston. The position is full-time for 3 months with an hourly rate of £32.37. You must be HCPC registered and ready to contribute to a dynamic microbiology team in a supportive environment. You will perform diagnostic microbiology tests, collaborate with colleagues, manage data, and uphold laboratory safety and quality standards in a busy healthcare setting. #J-18808-Ljbffr

hackajob is partnering directly with Leonardo to hire for this role. Salary: £59,500 - £75,000 Leonardo UK operates a grade-based salary framework with broad bands. The salary range shown reflects the approved grade band for this role, or a narrower hiring range published within that band, and is benchmarked against the external market. Exceptions above the standard range are managed through governance controls to protect internal equity. At Leonardo, we solve real-world engineering challenges, designing and developing mission-critical solutions that power some of the worlds most advanced defence systems. We are looking for a highly motivated System Integration & Qualification Lead for the P4E Mk0 Radar Product. The successful candidate will lead the P4E System Integration and Qualification team, manage the integration environment and co-ordinate testing to support the delivery of the P4E product to the customer. This includes development of the Integration, verification and qualification strategies. The role offers significant exposure to all aspects of the Radar domain and presents an excellent development opportunity. • Generation of traceability through DOORS from top level system requirements into the ATD/Test Cards that contribute to release specific evidence generation, • Create Test, Integration, acceptance & verification plan that feeds into the SEDP, • Create Integration, • Create Test Cards, • Create Acceptance Test Descriptions, • Create Acceptance Test Procedure, • Creation of Lab specific scripting of test execution and analysis, • Create Test Reports, • Accurate and clear recording of defects, • Management of Hardware (Radar and Test Equipment), ensuring that demand is always met, • Support of System Problem Report (SPR) analysis and fix verification The successful candidate should be pro-active to ensure that the right strategy is in place & that the integration environments are ready and fit to meet the verification and qualification requirements. They should also be able to establish and maintain good lines of communication across the project, engineering disciplines and engineering management. • Authoring specifications and plans for Integration, Verification & Qualification, • Leading Test Readiness Reviews (TRRs), and being involved in PDRs and CDRs, • Experience of integration and test of a complex System in an integration lab environment, • Experience of DOORS, Jira & Confluence, • Prior management experience in organising a team of engineers and setting & tracking daily objectives, • Experience of DOORS for system requirements and traceability of testing, • Experience of working in an Agile project environment This role is subject to pre-employment screening in line with the UK Governments Baseline Personnel Security Standard (BPSS). An additional range of Personnel Security Controls referred to as National Security Vetting (NSV) may apply, this could include meeting the eligibility requirements for The Security Check (SC) or Developed Vetting (DV). For more information and guidance please visit: join us At Leonardo, our people are at the heart of everything we do. We offer a comprehensive, company-funded benefits package that supports your wellbeing, career development, and worklife balance. Whether you're looking to grow professionally, care for your health, or plan for the future, were here to help you thrive. • Time to Recharge: Enjoy generous leave with the opportunity to accrue up to 12 additional flexi-days each year., • Secure your Future: Benefit from our award-winning pension scheme with up to 15% employer contribution., • Your Wellbeing Matters: Free access to mental health support, financial advice, and employee-led networks championing inclusion and diversity (Enable, Pride, Equalise, Armed Forces, Carers, Wellbeing and Ethnicity)., • Rewarding Performance: All employees at management level and below are eligible for our bonus scheme., • Never Stop Learning: Free access to 4,000+ online courses via Coursera and LinkedIn Learning., • Refer a friend: Receive a financial reward through our referral programme., • Tailored Perks: Spend up to £500 annually on flexible benefits including private healthcare, dental, family cover, tech & lifestyle discounts, gym memberships and more., • Flexible working: Flexible hours with hybrid working options. For part time opportunities, please talk to us about what might be possible for this role. For a full list of our company benefits please visit our website. Leonardo is a global leader in Aerospace, Defence, and Security. Headquartered in Italy, we employ over 53,000 people worldwide including 8,500 across 9 sites in the UK. Our employees are not just part of a team they are key contributors to shaping innovation, advancing technology, and enhancing global safety. At Leonardo we are committed to building an inclusive, accessible, and welcoming workplace. We believe that a diverse workforce sparks creativity, drives innovation, and leads to better outcomes for our people and our customers. If you have any accessibility requirements to support you during the recruitment process, just let us know. GB - Edinburgh Permanent Onsite JBRP1_UKTJ #J-18808-Ljbffr

Associate Manager IQVIA Laboratories – Central Laboratory Service We are a comprehensive global central laboratory services supporting clinical trials in countries around the world. Meeting the demands of today’s drug, device and diagnostics development environment requires a next generation service provider. IQVIA Laboratories helps sponsors enable laboratory testing in global clinical trials by providing specimen collection kits, a courier network, a biorepository, plus project management and data management. With extensive scientific expertise and industry leading capabilities in lab services, biomarkers, companion diagnostics, esoteric testing, high quality data and analytics, as well as global logistics and biorepository & specimen management, IQVIA Laboratories helps biotech and pharmaceutical companies meet their development needs. Join us on our exciting journey! Responsible for supervising a team of lab staff and ensuring effective operational delivery and for setting day to day operational activities for the team with a focus on daily delivery. Under the mentorship of management, responsible for hiring, training, and performance management of staff. Supervises the daily activities of assigned laboratory work group(s) through appropriate delegation, technical skills training, and work supervision. Meets regularly with staff and senior management to discuss and resolve workload and technical issues. Responsible for ensuring activity in the team meets safety guidelines. Drives individual accountability for safety across the team. Identifies opportunities for improvements in safety. Responsible for the review of laboratory metrics to identify initiatives as well as establish additional metrics such as cost savings that are associated with process improvement initiatives. Ensures policies, practices and procedures are understood and followed by direct reports, customers and stakeholders. Ensures timely and appropriate resolution of CAPA and quality incidents, quality and compliance metrics, root cause analysis and improvement. Assists in establishment and revision of laboratory policies and procedures. Maintains appropriate control and quality assurance procedures. Ensures compliance with safety requirements. Bachelor’s degree in a Human Biology based science. 4 years of relevant experience in a clinical laboratory or clinical trials environment. (Biochem based) Experience in technical leadership and cross-functional collaboration Proficiency with LIMS and other laboratory data systems. Familiarity with CAPA processes and quality systems Ability to analyse and interpret complex data. Ability to effectively coordinate and execute multiple tasks or projects simultaneously. Ability to effectively write scientific and technical documents Understanding of LEAN 6 Sigma principles Join IQVIA to see where your skills can take you Global exposure Variety of therapeutic areas Collaborative and supportive team environment Access to cutting-edge and innovative, in-house technology Excellent career development and progression opportunities Work-Life Balance, with a strong focus on a positive well-being. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. #J-18808-Ljbffr

Keep 100% of your PT earnings, your first month is rent free. you will have access to the largest member base in the UK, plus: • You will have access to an exclusive app with industry leading content., • Free education and CIMSPA accredited courses all bespoke to PureGym, with unlimited access to business resources., • Access to the best fitness discounts exclusive to PG Personal Trainers., • Free Webinars, podcasts and access to our mentoring lab – you can be mentored on all aspects of your business., • Wellness package – Online GP, counselling sessions, Physio sessions & Financial guidance., • PT Support – 5x free guest passes per month, lead generation workshops, PT open week for you to generate leads & PT taster sessions on the timetable for members to discover you., • Full rent transition programme delivered by master trainers., • Free advertising on the PureGym website, social media and in club, • Contracted salary, guaranteed 12 hours per week., • Annual leave allowance, plus a personal day off., • Free Gym Membership for yourself and a friend or family member, • Employee Assistance Programme, • Pension Scheme, • Discounted legal services, • Enhanced maternity & paternity leave, • Funded First Aid qualification., • Career development with management training programmes, • Group Exercise initial training and continual upskill opportunities. you will play a key part in the safe enjoyment of our gyms, delivering an amazing member experience, teaching classes, inductions, and taking care of the upkeep of the gym floor. • A passion for fitness and wellbeing, • Someone who embodies ‘Feel PureGym good’ in all that they do. The PureGym Group is a global gym business with a community of more than 700 gyms and over 2 million members. At PureGym, everything we do comes back to one simple idea: helping you feel good. We’re proud of our people and have a strong focus on internal progression. Championing diversity, we are committed to providing an excellent employee experience and workplace culture. As such, we are a Disability Confident Committed employer, and offer interviews to candidates who meet the essential criteria for a role, and opt-in to the scheme on their application form. Our gyms are friendly, supportive, and judgement-free spaces where everybody can come in, work out and leave Feeling PureGym Good. We are proud to be certified byTop Employers Institute. Join us on our mission to inspire a healthier nation. #J-18808-Ljbffr

Reading, Berkshire, United Kingdom Manchester, United Kingdom London, United Kingdom Livingston, West Lothian, United Kingdom Full time R1560752 The Data Acquisition Specialist performs activities relating to the definition, set-up and ingestion of External Data Streams, and related documents and processes aligned with Clinical Trial Protocol defined requirements for data capture. External data streams include but are not limited to typical and novel data collected through central labs and ECG, medical imaging, biomarker and genomics analysis, real world data sources, EHR, electronic patient reported outcomes, wearables and sensors and other digital data collection technologies. • Execute deliverables for Standardized External Data Streams., • Assess external data collection requirements per protocol and planning of external data stream set-up activities and related deliverables to meet study start-up timelines., • Liaise with key data stakeholders to establish the purpose of data collection and requirements for the transfer, ingestion, and structure of data for each data stream in compliance with applicable data protection laws and regulations, utilizing available standards and templates, • Create change requests for the definition of new test concepts or data structures relating to external data., • Develop trial-specific Data Transfer Agreements (tsDTA's) accurately documenting study requirements and methods for the data transfer, ingestion, and structure., • Ensure data transfer frequencies are sufficient for the agreed requirements (medical data review, central monitoring, and reporting and analysis)., • Liaise with external data providers to ensure alignment and agreement of tsDTA., • Translate medical and scientific concepts into data mapping guidance, per agreed data model and documented in the annotated Data Transfer Agreement for use by Clinical programmers., • UAT of test data transfers ensure accuracy and consistency with data specifications defined in Data Transfer Agreements., • Implement data transfer mechanisms for external data streams (into CDR) including access for external data providers., • Monitor availability and accuracy of external data streams, liaise with external data providers to resolve data transfer issues relating to conformance of data., • Bachelor's degree or equivalent, preferably in Computer Science., • Minimum of 3 years' experience managing data in support of clinical research., • Experience working with external data e.g., Safety Lab, PK, Simple Biomarkers, ECG, etc, • Experience in working with external data providers within a clinical study setting., • Experience developing data transfer agreements., • Experience working on clinical trials., • Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional., • Knowledge of SDTM., • Working knowledge of GCP/ICH guidelines, • Excellent written and verbal communication in English.This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. #J-18808-Ljbffr

We are a comprehensive global central laboratory services supporting clinical trials in countries around the world. Meeting the demands of today's drug, device and diagnostics development environment requires a next generation service provider. IQVIA Laboratories helps sponsors enable laboratory testing in global clinical trials by providing specimen collection kits, a courier network, a biorepository, plus project management and data management. With extensive scientific expertise and industry leading capabilities in lab services, biomarkers, companion diagnostics, esoteric testing, high quality data and analytics, as well as global logistics and biorepository & specimen management, IQVIA Laboratories helps biotech and pharmaceutical companies meet their development needs. Responsible for supervising a team of lab staff and ensuring effective operational delivery and for setting day to day operational activities for the team with a focus on daily delivery. Under the mentorship of management, responsible for hiring, training, and performance management of staff. Supervises the daily activities of assigned laboratory work group(s) through appropriate delegation, technical skills training, and work supervision. Meets regularly with staff and senior management to discuss and resolve workload and technical issues. Responsible for ensuring activity in the team meets safety guidelines. Drives individual accountability for safety across the team. Identifies opportunities for improvements in safety. Responsible for the review of laboratory metrics to identify initiatives as well as establish additional metrics such as cost savings that are associated with process improvement initiatives. Ensures policies, practices and procedures are understood and followed by direct reports, customers and stakeholders. Ensures timely and appropriate resolution of CAPA and quality incidents, quality and compliance metrics, root cause analysis and improvement. Assists in establishment and revision of laboratory policies and procedures. Maintains appropriate control and quality assurance procedures. Ensures compliance with safety requirements. • Bachelor's degree in a Human Biology based science., • 4 years of relevant experience in a clinical laboratory or clinical trials environment. (Immunology based), • Experience in technical leadership and cross-functional collaboration, • Proficiency with LIMS and other laboratory data systems., • Familiarity with CAPA processes and quality systems, • Ability to analyse and interpret complex data., • Ability to effectively coordinate and execute multiple tasks or projects simultaneously., • Ability to effectively write scientific and technical documents, • Understanding of LEAN 6 Sigma principles, • Global exposure, • Variety of therapeutic areas, • Collaborative and supportive team environment, • Access to cutting-edge and innovative, in-house technology, • Excellent career development and progression opportunities, • Work-Life Balance, with a strong focus on a positive well-being. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. #J-18808-Ljbffr

We are a comprehensive global central laboratory services supporting clinical trials in countries around the world. Meeting the demands of today’s drug, device and diagnostics development environment requires a next generation service provider. We are a comprehensive global central laboratory services supporting clinical trials in countries around the world. Meeting the demands of today’s drug, device and diagnostics development environment requires a next generation service provider. IQVIA Laboratories helps sponsors enable laboratory testing in global clinical trials by providing specimen collection kits, a courier network, a biorepository, plus project management and data management. With extensive scientific expertise and industry leading capabilities in lab services, biomarkers, companion diagnostics, esoteric testing, high quality data and analytics, as well as global logistics and biorepository & specimen management, IQVIA Laboratories helps biotech and pharmaceutical companies meet their development needs. Join us on our exciting journey! Responsible for supervising a team of lab staff and ensuring effective operational delivery and for setting day to day operational activities for the team with a focus on daily delivery. Under the mentorship of management, responsible for hiring, training, and performance management of staff. Supervises the daily activities of assigned laboratory work group(s) through appropriate delegation, technical skills training, and work supervision. Meets regularly with staff and senior management to discuss and resolve workload and technical issues. Responsible for ensuring activity in the team meets safety guidelines. Drives individual accountability for safety across the team. Identifies opportunities for improvements in safety. Responsible for the review of laboratory metrics to identify initiatives as well as establish additional metrics such as cost savings that are associated with process improvement initiatives. Ensures policies, practices and procedures are understood and followed by direct reports, customers and stakeholders. Ensures timely and appropriate resolution of CAPA and quality incidents, quality and compliance metrics, root cause analysis and improvement. Assists in establishment and revision of laboratory policies and procedures. Maintains appropriate control and quality assurance procedures. Ensures compliance with safety requirements. • Bachelor’s degree in a Human Biology based science., • 4 years of relevant experience in a clinical laboratory or clinical trials environment. (Biochem based), • Experience in technical leadership and cross-functional collaboration, • Proficiency with LIMS and other laboratory data systems., • Familiarity with CAPA processes and quality systems, • Ability to analyse and interpret complex data., • Ability to effectively coordinate and execute multiple tasks or projects simultaneously., • Ability to effectively write scientific and technical documents, • Understanding of LEAN 6 Sigma principles Join IQVIA to see where your skills can take you • Global exposure, • Variety of therapeutic areas, • Collaborative and supportive team environment, • Access to cutting-edge and innovative, in-house technology, • Excellent career development and progression opportunities, • Work-Life Balance, with a strong focus on a positive well-being. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. #J-18808-Ljbffr

Platform Recruitment is seeking an Electronics & Mechanical Technician in Linlithgow, Scotland, to support the engineering lab and develop power electronics prototypes and test rigs. You will assemble, wire, test and maintain prototype hardware, manage lab equipment, and work across electronics and

We are a comprehensive global central laboratory services supporting clinical trials in countries around the world. Meeting the demands of today’s drug, device and diagnostics development environment requires a next generation service provider. IQVIA Laboratories helps sponsors enable laboratory testing in global clinical trials by providing specimen collection kits, a courier network, a biorepository, plus project management and data management. With extensive scientific expertise and industry leading capabilities in lab services, biomarkers, companion diagnostics, esoteric testing, high quality data and analytics, as well as global logistics and biorepository & specimen management, IQVIA Laboratories helps biotech and pharmaceutical companies meet their development needs. Join us on our exciting journey! Job Overview: Responsible for supervising a team of lab staff and ensuring effective operational delivery and for setting day to day operational activities for the team with a focus on daily delivery. Under the mentorship of management, responsible for hiring, training, and performance management of staff. Supervises the daily activities of assigned laboratory work group(s) through appropriate delegation, technical skills training, and work supervision. Meets regularly with staff and senior management to discuss and resolve workload and technical issues. Responsible for ensuring activity in the team meets safety guidelines. Drives individual accountability for safety across the team. Identifies opportunities for improvements in safety. Responsible for the review of laboratory metrics to identify initiatives as well as establish additional metrics such as cost savings that are associated with process improvement initiatives. Ensures policies, practices and procedures are understood and followed by direct reports, customers and stakeholders. Ensures timely and appropriate resolution of CAPA and quality incidents, quality and compliance metrics, root cause analysis and improvement. Assists in establishment and revision of laboratory policies and procedures. Maintains appropriate control and quality assurance procedures. Ensures compliance with safety requirements. Requirements: • Bachelor’s degree in a Human Biology based science., • 4 years of relevant experience in a clinical laboratory or clinical trials environment., • (Immunology based) Experience in technical leadership and cross-functional collaboration, • Proficiency with LIMS and other laboratory data systems., • Familiarity with CAPA processes and quality systems, • Ability to analyse and interpret complex data., • Ability to effectively coordinate and execute multiple tasks or projects simultaneously., • Ability to effectively write scientific and technical documents, • Understanding of LEAN 6 Sigma principles Company Culture and Benefits: • Join IQVIA to see where your skills can take you, • Global exposure, • Variety of therapeutic areas, • Collaborative and supportive team environment, • Access to cutting-edge and innovative, in-house technology, • Excellent career development and progression opportunities, • Work-Life Balance, with a strong focus on a positive well-being. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. #J-18808-Ljbffr

Overview In this Clinical Specialist role, you will provide clinical and technical support for Gore’s Aortic Endovascular devices within the UK. You will work closely with vascular surgeons and interventional radiologists, guiding case planning, device sizing, and imaging review to support patient outcomes. You’ll act as the knowledge expert for Gore Aortic Devices, delivering training, presentations, and hands-on education at workshops and conferences. You’ll collaborate with hospitals and education centers, analyze market needs, and help drive clinical education and promotional activities. This role offers clinical influence, cross-functional teamwork, and opportunities to shape endovascular care, Pay / Benefitscomprehensive benefitsAssociate Stock Ownership Planpotential profit-sharingflexible benefitswell-being programscompetitive total rewards ResponsibilitiesProvide high level clinical and technical support in Gore Aortic Endovascular procedures in OR or vascular labConsult with Vascular Surgeons and Interventional Radiologists; read CTs, plan cases, size and select devicesBuild strong, trust-based relationships with clinicians and key opinion leadersPartner with hospitals and centers of excellence to deliver clinical product training and presentationsServe as the knowledge expert for Gore Aortic Devices and disease statesLead high-value education at UK workshops with simulators, demo devices, and flow modelsAnalyze market to plan objectives/actions according to business unit guidelinesEngage with hospital administrations and nursing teams across stakeholdersAttend UK/European congresses and support local sales promotions for education and business needsBe an active member of a highly experienced team Key requirementsProactive, driven and self-motivatedExcellent verbal and written communication skillsAbility to build trust-based relationships with physician customers and internal stakeholdersGenuine clinical interest and commitment to successful patient outcomesOrganized, flexible, and responsive with a strong sense of urgencyPassionate about medical devices and strong team playerDesire to become a specialist and consultative partner for customersAbility to plan, deliver, and follow up with customers to drive business successExperience in implantable Medical Devices in either sales or clinical supportIdeally a medical engineering or clinical background in Vascular/Cardiac Interventional or Medical Implantable DevicesDegree educated in science, technical or clinical discipline preferredAbility to travel across UK (about 70% travel) to support customers, meetings, conferences, trainingsLocated near a major UK airportRelationship-buildingStrong communicationProactivityClinical support for implantable medical devicesCT interpretation and case planningDevice sizing and selection

Bradley Environmental Consultants, powered by Vadella, seeks a Part-Time P401 Qualified Laboratory Analyst to join our UKAS-accredited laboratory in Livingston.

TRS Consulting seeks a Field Service Engineer to service and repair high-value medical and laboratory diagnostic equipment across NHS and private labs.

IQVIA Laboratories – Central Laboratory Service in the UK is seeking an Associate Manager to lead a laboratory team, ensuring high-quality operational delivery and adherence to safety standards.You will mentor staff, drive CAPA and quality initiatives, and work closely with management to resolve w

IQVIA Laboratories – Central Laboratory Service is seeking an Associate Manager to oversee lab teams and drive daily operational delivery. You will mentor staff, manage performance, and ensure safety and quality standards across the department. The role involves reviewing metrics, implementing process improvements, and collaborating with cross-functional teams to meet project timelines. A strong background in LEAN Six Sigma and data interpretation is essential. #J-18808-Ljbffr

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. The Eurofins network is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across its companies around the world. We’re proud to be an armed forces-friendly place to work and welcome applications from reservists, armed forces veterans (including the wounded, injured and sick), as well as cadet instructors, and military spouses and partners. Unfortunately we do not offer sponsorship for this role. Full time, permanent. Working hours: Monday - Friday, 9:00 - 17:00. 4 days per week based in Linlithgow and 1 day per week based in Livingston. Purpose of the post As Business Administrator, you will provideto all departments within both of our Laboratories, duties include: • Provide administrative support, to all areas of the business, with focus on operations, finance and purchasing., • Handle incoming communication and provide information to other finance departments within the organisation and suppliers., • Provide further information, such as copy invoices & statements, as required to facilitate payment., • Manage buildings and facilities related issues including H&S administration– both internal and external, • Liaise with Eurofins Account Receivable team to accurately assign and record credit notes and payments., • Responsible for creating and managing blanket Pos for all services required for the buildings or the labs., • Responsible for arranging services i.e. printers, tenancy queries, and utilities as and when required to ensure business runs smoothly, using suppliers listed on Coupa and making payment. All service invoices utilities/rates/waste/ and any further ad hoc suppliers, • Coordinate travel and events where required., • Utilise MS Office tools (Excel, Teams, Outlook, etc.) to communicate., • Use various software systems (internal Eurofins and MS Access) to track performance and provide additional information, • Arrange PUID numbers and Access Cards for all new Eurofins employees., • Provide a high level of internal and external customer care., • Maintain and administer company records, systems, assets, contracts and business processes Our ideal candidate will have experience in the following: • Understanding of finance, AR, AP, • Experience in working in part of a team, • Understanding of COUPA, • Experience of work in an administrative role., • MS Office, • Good organisation and time management, • Good verbal and written communication skills, • Ability to self-manage, • Flexible and supportive approach., • Experience in a finance related role (desirable, not essential), • Good Excel Skills, e-LIMS FGS and MS related software(desirable, not essential), • Hands on experience with Coupa(desirable, not essential), • Experience of work in lab testing company(desirable, not essential) At 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: • Additional Annual Leave at Employees set service dates, • Company Pension Plan, • Life Assurance Scheme (4 times annual salary), • Healthcare Cash Plan (6+ months service), • Enhanced Maternity, Adoption and Paternity Schemes, • Employee Assistance Programme – 24/7 confidential, • Health and Wellbeing Programmes, • Free parking, • Worldwide career opportunities, • We also have in place rewards recognising the great work ouremployees deliver, their dedicated service and celebrating special life events. What Happens Next Our 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. Weembracediversity!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. By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply #J-18808-Ljbffr

IQVIA Laboratories – Central Laboratory Service is recruiting an Associate Manager to supervise a lab team in Livingston, UK. You will oversee daily operations, guide staff performance, and coordinate with management to meet safety and quality goals. With a Bachelor’s in Human Biology-based science and 4+ years in a clinical lab or trials setting, you will apply CAPA processes, LEAN 6 Sigma principles, and data-driven improvements to ensure high-quality outcomes across multiple projects. #J-18808-Ljbffr

Eurofins Scientific in Linlithgow is seeking a part-time Laboratory Assistant for the Food Microbiology department.The role covers sample preparation, media setup, quality checks, and general lab support, with fixed 24-hour weekly schedule: Thursday and Friday 11:00-19:30, Saturday 08:30-17:00.You w

Pertemps Medical Professionals is actively recruiting a Band 6 Cardiac Radiographer to join a busy Cath Lab team in Stoke-on-Trent. You will perform a range of Cath Lab imaging procedures, operate Philips equipment to produce high-quality images, and support procedures such as coronary angiography a

The successful candidate will learn about the ABE process, gain hands-on laboratory experience, and participate in structured training at Forth Valley College. This role provides foundational knowledge in Good Lab Practice and requires attention to detail, organization, and a keen interest in scienc

Field Service Engineer role focusing on laboratory or biomedical equipment, offering flexibility and autonomy within a global company.

The Role: Sell specialist products, bespoke industrial furnaces and ovens- training provided Provide support for clients and discuss technical issues Upsell existing products and win new business Travel to meet customers and carry out quotations The Person: Technical Sales experience R&D / Lab / Res

An experienced Asbestos Lab Analyst is needed to analyze asbestos samples using PLM and stereo-microscopy, update databases, and issue certificates to maintain UKAS accreditation.

Seeking a detail-oriented Asbestos Lab Analyst with hands-on experience in bulk analysis of ACMs for a UKAS accredited specialist in Harlow, Essex.

Seeking a Lab Technician / Junior Lab Technician to join a family-run business in Portsmouth, focused on electronics testing and laboratory environments.

Do you have Technical Sales and R&D / Lab / Research Equipment experience? On offer is a varied role where you can upskill yourself on a specialist product range within a dynamic, growing company who. Technical Sales Consultant (R&D / Lab Equipment).

Asbestos Lab Analyst role focused on analyzing bulk material samples in a laboratory setting.

A professional and established Asbestos Consultancy are now seeking to take on an Asbestos Lab Analyst to join their longstanding lab in the South Coast area. Alternative Job titles: Asbestos Lab Analyst, Environmental Lab Analyst, Bulk Sample Analyst. Will have experience working hands on within an

Seeking a skilled Data Center ICT Lab Engineer for a 6-month contract role in South Yorkshire to support on-prem IT infrastructure.

Seeking an Asbestos Lab Analyst for a consultancy in Eastleigh, Hampshire. Requires BOHS P401 qualification and UKAS accredited lab experience.

ACTUAL CLOSING DATE: Applications must be received by Thursday 22 October 2026 at 11:55pm.Please ensure that you read the full advert text and do not submit a CV, as these will be disregarded as they do not form part of SLC application process.If you require to submit additional information to supp

Join the UK's Favourite Parcel Delivery Company!.Christmas Incentive 2026 - Earn an EXTRA 50p for every stop*.To qualify and be paid before Christmas Eve, simply:.Deliver parcels on our busiest days.At DPD, we provide the tech, start up support, and steady volume you need to build a high-earning r

Support Worker – Linlithgow, West Lothian (EH49).Three decades supporting people across health and social care.We do what is right, even when no one is watching.Compassionate care starts with you.Join our team in Linlithgow and help people live fuller and more independent lives.Deliver person cent

Permanent, 14% shift allowance.Deans House is a residential care home for adults with learning disabilities based in Livingston.The service supports individuals to engage in a wide range of meaningful community activities, helping them achieve their personal outcomes, goals and aspirations.We promot

Waverley Residential Home, Galashiels.SVQ2 or equivalent is desirable but not essential.You can earn whilst you learn!.PVG Adults – we will do this for you! SSSC registered.We focus on these five principles to provide excellent care through a well-structured, meaningful and person-centred approach

Candidates must be available to cover the shifts detailed below as required Mon to Sun throughout the year.

Enable creates a bespoke team around every individual we support, and our team of Personal Assistants work collaboratively to ensure the safety, wellbeing and aspirations of the people we support are met.

An exciting opportunity has arisen to join our learning community within Dedridge Primary School ( Glenvue Nursery_.Dedridge PS is non-denominational primary school and nursery, serving part of the community of Dedridge in West Lothian.The school is situated in an area of multiple deprivations.The n

Please note that sponsorship is not available, or being offered, in connection to this post.

West Lothian Council reserve the right to close this post early depending on applicant response levels.Krikhill Primary School and nursery situated in the Broxburn area of West Lothian and the nursery is located in the Primary School building.We have a range of full time and half day placements and

An opportunity has arisen for a Pupil Support Worker to join the Nursery team at Letham Primary School.Working as part of a dedicated and enthusiastic Early Years team, the successful candidate will support the delivery of high-quality early learning and childcare that meets the needs of young child