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Quality Manager- Medical Devices Birmingham, UK On site We are a leading diagnostics company seeking an experienced Quality Manager to join our team. This role will be responsible for maintaining and developing our Quality Management System while ensuring regulatory compliance across our diagnostic operations in the UK and ROI. This is a key leadership role working closely with senior management to drive quality excellence, regulatory compliance, and continuous improvement across the organisation. Key Responsibilities • Maintain and develop the Quality Management System (QMS) and ensure continued ISO9001 certification, • Support continued UKAS accreditation (ISO17025) across calibration facilities, • Ensure ongoing compliance with regulatory requirements and applicable legislation, • Act as Management Representative for the quality system, • Lead internal audits and support external audit programmes, • Manage the Management Review process and report on QMS performance, • Lead CAPA activities, root cause investigations, and corrective actions, • Monitor and report on non-conforming products and market quality issues, • Drive continuous improvement initiatives based on operational data and customer feedback, • Oversee the Quality Surveillance programme, • Act as Q-Pulse System Administrator including documentation, CAPA, audits and COSHH management, • Lead New Product Introduction (NPI) quality processes, • Work cross-functionally with internal teams, suppliers and customers on quality matters, • Degree or equivalent qualification, • Strong understanding of the medical device or diagnostics industry, • Excellent knowledge of ISO9001, ISO13485 and ISO17025, • Lead auditor qualification or demonstrable auditing experience, • Strong analytical and problem-solving skills with high attention to detail, • Excellent organisational and time management skills, • Strong interpersonal and stakeholder management abilities, • Ability to work both independently and collaboratively across teams, • Excellent written and verbal communication skills We are looking for a proactive and solution-focused Quality professional who can lead quality initiatives, influence stakeholders, and drive continuous improvement across the business. The successful candidate will be highly organised, collaborative, and comfortable working in a fast-paced operational environment. To apply - please apply via this advert! Look forward to receiving your applications!

Title: Technical Assessor Location: West Midlands Salary: £30,000 - £35,000 DOE Type: Permanent Benefits: Ongoing career development and progression, pension SRG are working with an independent and growing waste management and environmental services company. With decades of industry experience, they are deeply committed to their values and their people. They invest heavily in their team, offering robust training and development opportunities to support long-term growth and success. They are now looking for an experienced Technical Assessor to join the team. The successful candidate will be responsible for the compliance, safety and classification of waste following the relevant regulatory guidelines. This would suit candidates with 1+ years’ experience as a technical assessor or a site chemist position in the waste industry. Working Hours: onsite 5/5 Monday –Friday, 25 days holiday + 8 bank holidays, Role / Description • Conduct technical assessments of waste management operations to ensure compliance with environmental and industry regulations., • Work alongside site chemists and mobile chemists to provide technical assessments on waste coming into site as well as customer sites, • Qualification and classification of chemicals, reporting and analysis of waste streams to determine what can be treated onsite and what needs transferring to other sites, • Identify and assign cost effective treatment and processing routes, • Evaluate applications for permits, accreditations, or certifications related to waste processing, recycling, and disposal., • Provide expert advice on waste classification, handling, treatment, and disposal methods., • Liaise with regulatory bodies, clients, and internal teams to ensure consistent interpretation of waste legislation and best practices., • Analysis of information to determine waste transportation methods (ADR/IMDG regs), • Work alongside DGSA’s, management, sales and chemists to facilitate smooth running of inbound and outbound waste streams., • Provide technical advice, support and guidance internally and externally Requirements • Minimum HNC any of the following degrees Chemistry, bio chemistry, environmental science, biochemistry or scientific degree with significant chemistry content, • Recent experience working as a technical assessor or a site chemist in the waste industry, • DGSA, IOSH and IMDG– preferred, • Knowledge and understanding of ADR, WM3 and other waste regulations SRG is the UK’s number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors. If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV to . For more information regarding this position or any others, please call Rhi on 0161 667 1812. If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit to view our other vacancies. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It’s this combination that makes us different. We’re committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients. Keywords: waste, hazardous waste, chemist, chemicals, chemistry, waste analysis, reception chemist, site chemist, acceptance chemist, waste chemist, environmental, health and safety, H&S, IOSH, WAMITAB, NEBOSH, waste management, recycling, technical, technical assessor, waste streams, wm3, IMDG, ADR, COSHH, SDS, PIF, Product information file, Safety Data Sheet

NPI Consultant – Biotech (Drug-Device Combination Product) I’m currently supporting an innovative and rapidly growing biotech organisation in the search for an NPI Consultant to support a key programme within respiratory drug-device combination products. The role This is a hands-on NPI position focused on supporting the introduction and development of a complex combination product. You will work cross-functionally with technical, quality, and development teams to ensure smooth progression through key development milestones. Key responsibilities • Support New Product Introduction (NPI) activities across development programmes, • Collaborate with cross-functional teams across R&D, Quality, and Supply Chain, • Ensure alignment between product development, manufacturing, and regulatory requirements, • Contribute to planning and execution of development and scale-up activities, • Support documentation and processes required for clinical-stage products Requirements • Strong experience in NPI within biotech, pharma, or medical devices, • Experience working with drug-device combination products (highly desirable), • Background supporting clinical-stage development programmes, • Solid understanding of GxP environments and product lifecycle development, • Ability to work in a cross-functional, fast-paced environment About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Finlay Keyworth (Recruiter II) at Planet Pharma for more information: E:

Healthcare Solicitor – Birmingham Our client is looking to recruit Associates at all levels to join its Healthcare team, following continued growth across our UK offices. Why Join Our Client? • Hybrid working, • 25 days' holiday plus option to buy more, • Pension scheme, health cash plan, life assurance and income protection, • You will work closely with a Partner advising on a broad range of healthcare matters, including:, • Representation at inquests, • Advising clinicians in regulatory proceedings, • Medical device and product liability claims, • Advising on complex healthcare and professional liability matters, • Drafting and interpreting complex legal documentation, • Managing claims involving breaches of professional standards, • Liaising with clients, witnesses and stakeholders, • Preparing court documents and supporting litigation strategy, • Contributing to seminars, publications and client events, • Identifying business development and cross-selling opportunities, • Ideally 1+ years' PQE, • Experience in defended clinical negligence/medical malpractice work, • Exposure to high-value or multi-million-pound claims preferred, • Experience within the healthcare sector, • Strong technical ability, initiative and case management skills #INDMALN

The Opportunity We are an Imperial College London med tech spinout building AI-powered clinical decision-support tools certified as Software as a Medical Device (SaMD). Our platform uses real-world EHR data to identify patients at risk of preventable harm — giving NHS clinicians time to act. We are a small, high-ownership team operating at the intersection of clinical AI and healthcare infrastructure. This is a foundational engineering hire with a clear path to Head of Engineering as we scale. The Role You will own and shape the technical core of a live clinical AI platform — working across backend services, ML infrastructure, and hospital data integrations. You will have a direct line to the CTO and CEO from day one, with real influence over architectural decisions on a system processing real patient data across NHS trusts. What You'll Do 🔹 Own and extend the backend and ML infrastructure of a production SaMD system 🔹 Design and implement integrations with hospital systems (EHR, HL7/FHIR), including partnerships with major healthcare data platforms 🔹 Build and maintain Python/Azure-based services — APIs, data pipelines, monitoring and audit frameworks 🔹 Write software that meets medical device quality standards, producing artefacts that support regulatory submissions 🔹 Collaborate with clinical, data science, and regulatory stakeholders 🔹 Help define engineering culture and processes as the team grows around you What We're Looking For ✅ 5+ years of professional software engineering experience with a strong Python background ✅ Proven experience building and operating production services on Azure or AWS ✅ Comfort with data-heavy systems — pipelines, databases, REST APIs — and a taste for clean architecture ✅ Strong written communication; able to document work to regulatory audit standard Nice to Have ⭐ Experience in a regulated software environment (medical devices, fintech, defence, or similar) ⭐ Familiarity with FHIR/HL7 or clinical EHR systems ⭐ Exposure to ML model deployment or monitoring in production Tech Stack Python · Azure · Terraform · Docker · ML Pipelines · FHIR / HL7 · GitHub Actions What's on Offer 💰 Competitive renumeration package, depending on experience 🏖️ 25 days annual leave + bank holidays 🏥 Access to clinical and academic networks 🔀 Flexible hybrid working, London base Growth Path As we move through our next funding round and scale clinical deployments, the expectation is that you grow into Head of Engineering or equivalent — owning technical strategy, building a team, and sitting at the table for product, regulatory, and commercial decisions.

Medical Field Service Engineer, Pathology Laboratory Diagnostics • Overall Earnings Circa £50,000, • Basic Salary £40,000 to £44,000, • Bonus 10%, • Company Car or Car Allowance, • Pension (5% employer contribution), • Healthcare, • Phone, Laptop and iPad, • 27 Days Holiday Plus Bank Holidays This market leader seeks to recruit a technically motivated and customer focused Medical Field Service Engineer, responsible for: • The service, installation, breakdown, repair and calibration of a wide range of sophisticated medical laboratory diagnostics systems, utilised within pathology departments, NHS laboratories and clinical chemistry environments To succeed in this exciting role, you must be able to demonstrate: • A competent background in a customer facing field service engineering capacity gained within any high value capital equipment environment, • Applications are encouraged from engineers with a broad range of backgrounds, including laboratory device, medical device, pharmaceutical device, ex forces engineers (medical & dental, weapons systems, radar) and a wide range of other electronic or electro-mechanical sectors, • Engineers with experience of the diagnostics field, including autoimmune diagnostics, immunology, biochemistry, haematology, histology, microbiology and immunodiagnostics systems are also encouraged to register their interest, • A qualification in engineering, electronics or a science based subject to a minimum of ONC level, City & Guilds or NVQ, • Well respected supplier of sophisticated medical diagnostics systems, trusted by healthcare professionals to accurately diagnose and test patients for a wide range of medical conditions and diseases, • This instantly recognisable brand leader supplies a wide range of innovative diagnostic based laboratory and medical systems to the healthcare sector, and offers 'best in class' solutions across their range of products and systems, which include applications for microbiology, immunodiagnostics, molecular diagnostics and blood bank screening JBRP1_UKTJ

Evolve are working with a well-established healthcare organisation to recruit a Territory Manager covering the West Midlands territory (specifically Shropshire, Black Country, Birmingham & Solihull) This is an opportunity to represent a highly respected Wound Care portfolio, offering clinically driven solutions that make a genuine difference to patient outcomes. You’ll have full ownership of your territory, supported by a collaborative team and a business that values long-term growth and partnerships. What’s in it for you? * Excellent Salary & Benefits - A competitive starting salary of, plus benefits! * Strong Global Presence - Established footprint across multiple international markets, offering stability and the opportunity to work within a well-recognised healthcare leader. * People-Centric Environment - Collaborative and supportive culture where employees are valued, encouraged, and given the tools to succeed. Ideal Requirements * Existing experience of either Medical Device, Healthcare or Pharmaceutical sales * Proven ability to influence and build relationships with key stakeholders * Healthcare sales experience with strong data analysis and territory planning skills * Target-driven with a consistent track record of delivering results * Experience within wound care is highly desirable, with a strong understanding of the market and clinical environment Role Responsibilities * De...

Company Description Jet Aire are a leading drainage provider working throughout the UK. This is an opportunity for a highly organised individual to join our growing no dig CIPP lining division delivering works for our growing division. We have grown the fleet significantly and have top of the range innovative equipment. Job Description Excavation Engineer Hebburn Permanent, full-time Competitive salary, Enhanced Overtime Rates plus benefits You will carry out all aspects of drain installation and repair, including excavating, trench support and reinstatements. More about the role: Key Responsibilities • Working in confined spaces, • Drain installation and repair including Section 104 work, CIPP Lining and Patch Repair, • Thorough completion of site/works information on a tablet device, • Carry out work in line with company health and safety policy and procedures, • Good time management and working efficiently, • Completing Drivers Hours Books and Vehicle Checks (Defect books), • General maintenance and upkeep of vehicles and equipment, • Be prepared to work weekends and away from home, • Undertake all training and development as required, • To understand risk assessments and to assess according to safe systems of work., • Able to understand and carry out work as set out in a specification., • Undertaken training on General Health & Safety awareness/ Risk Assessment awareness/Traffic Management/ Use of PDA as required by the company., • Driving license required (preferably including towing over 750kg), • CSCS Card required, • Full Street Works accreditation (operative or supervisor), • Excavator up to 20 ton (preferred), • Forward tipping dumper, • Confined Space Accreditation - Medium Risk, • Driven and enthusiastic, • Excellent customer service and communication skills, • Focus, thoroughness and keen attention to detail, • Solid problem solving and decision-making ability, • Commitment to service excellence demonstrating a 'can do' attitude, • Ability to work under pressure and to deliver results to strict/tight deadlines, • Absolute willingness to work outside in all weather conditions, • Work on the Public Highway, • Professional and flexible approach to work, • Drain lining and patching experience (preferred), • Enhanced maternity, paternity and adoption pay and leave, • Company pension, • Life assurance scheme (x4 salary), • Medicare Cash Plan (includes cash payments towards dental, medical, therapeutic treatments) with the option to add up to 4 dependants, • Refer a friend scheme, • Employee assistance programme (access to GP appointments and mental health support), • Competitive annual leave plus bank holidays, • Training and career progression opportunitiesAdler and Allan are committed to fostering diversity and inclusion in our workplace. We proudly embrace equal opportunities for all applicants, regardless of race, colour, religion, sex, sexual orientation, gender identity or national origin. If you require any support with your application, whatever the circumstance, please let us know. JBRP1_UKTJ

Job Description Drainage Operative Wellington - Commutable Distance Permanent - 40 Hours Competitive salary + Enhanced Overtime Rates, Stop out wok and Syphon Incentive available plus Company benefits Kickstart your career as a Drainage Operative and help us enhance wastewater systems and prevent pollution, while building a hands-on career. As a Drainage Operative you will firstly get to grips with the basics of working in the drainage field. You will learn the ropes, working with our experienced teams on either CCTV or Jetting vehicles, building an understanding on how we approach jobs using best practice. We work for the local water authority inspecting and maintaining drainage routes, for building companies cleaning and surveying pipes prior to completion and there are also multiple opportunities to be involved and assist in larger scale projects taking place in other departments within the company, such as tank and syphon cleaning. Once the initial training has been completed you will have developed a varied knowledge on how to approach jobs, select supplies required and, how to expertly use the equipment, assisting the vehicle lead to approach and complete jobs effectively. About the role: • High Pressure Water Jetting., • Working in confined spaces., • Driving and operating Van Packs, variety of CCTV vehicles & Jetting rigs across the fleet., • Manual Handling, Carrying Suction Hose, cleaning up spillages and removing debris using brushes, shovels etc., • Cleaning of sewer and storm lines using a high pressure unit or aiding with the Recycler team., • Assist the vehicle lead to achieve timely job completion., • Undertake all training and development as required., • Thorough completion of site/works information on a tablet device., • Can do/will do' attitude., • Flexible approach to work., • Be polite and approachable, • Effective timekeeping., • You must be a team player., • Willing to travel and stay away on a regular basis., • Full clean UK Driving Licence., • Enhanced maternity, paternity and adoption pay and leave, • Company pension, • Life assurance scheme (x4 salary), • Medicash Plan (includes cash payments towards dental, medical, therapeutic treatments) with the option to add up to 4 dependants, • Refer a friend scheme, • Employee assistance programme (access to GP appointments and mental health support), • Competitive annual leave plus bank holidays JBRP1_UKTJ

AssureBio is supporting a globally established pharmaceutical organisation in the appointment of a GVP QA Manager to strengthen its R&D Quality Assurance function. This is a high-impact role focused on pharmacovigilance quality oversight, vendor governance and regulatory inspection readiness within a global environment. You will operate as a key Quality Subject Matter Expert, ensuring robust compliance, patient safety and proactive regulatory readiness across pharmacovigilance and wider GxP activities. The position offers strong cross-functional exposure, working closely with senior stakeholders, global partners and regulatory bodies. Key Responsibilities GVP & R&D Quality Oversight • Provide leadership across pharmacovigilance QA activities within R&D and Scientific functions, • Act as SME for GVP/GxP compliance and provide expert regulatory interpretation, • Maintain oversight of Pharmacovigilance System Master File (PSMF) integrity, • Support quality due diligence for new product opportunities Audit & Vendor Management • Develop and maintain the R&D audit schedule, • Lead internal, vendor and third-party audits (acting as Lead or Co-Auditor), • Oversee quality performance of PV vendors and service providers, • Ensure effective audit closure and CAPA tracking Inspection Readiness & Compliance • Support regulatory inspection preparation and hosting (MHRA, EMA, FDA and global authorities), • Lead CAPA management arising from inspections and audits, • Provide risk-based QA advice to cross-functional teams, • Review and approve deviations, change controls and quality events Quality Systems & Continuous Improvement • Generate and present R&D quality metrics to senior stakeholders, • Deliver GxP training and guidance across the organisation, • Maintain awareness of evolving regulatory expectations and ensure business readiness, • Support continuous improvement of quality systems and processes This role is central to ensuring high standards of pharmacovigilance compliance, vendor oversight and inspection readiness across a complex global environment. Experience & Qualifications Essential • Scientific degree (Pharmacy, Chemistry, Biology, Engineering or related) or equivalent experience, • Significant QA experience within pharmaceutical and/or medical device environments, • Strong expertise in Good Pharmacovigilance Practice (GVP), • Proven experience supporting regulatory inspections and PV teams, • Experience in auditing, CAPA management and quality systems oversight, • Ability to operate autonomously and make risk-based quality decisions Desirable • Certification in auditing or Quality Systems Management, • Working knowledge of Good Clinical Practice (GCP), • Experience managing PV vendors and service providers, • Strong stakeholder engagement and influencing skills Candidates must demonstrate the ability to operate independently, provide strategic quality input and maintain strong regulatory compliance across global PV operations.

Are you passionate about automation and looking to lead cutting-edge projects in a collaborative, multi-disciplinary environment? Our client, 3P Innovation, are a leader in automated machinery for the pharmaceutical, medical device, and FMCG industries, and they are seeking a Senior Controls Systems

Field Service Engineer, Medical Diagnostic Systems Overall Earnings £60,000+ Basic Salary Up To £52,000 Overtime On Call Allowance 10% Bonus Company Car (Electric Or Hybrid) Pension Healthcare Life Insurance Phone, Laptop Holidays The role will involve working one weekend in four (during this week you will receive two alternative days off work) The Role – Field Service Engineer, Medical Diagnostic Systems This market leader seeks to recruit a technically motivated and customer focused Field Service Engineer, responsible for: The service, installation, breakdown, repair and calibration of a wide range of sophisticated laboratory diagnostics systems utilised within pathology departments, NHS laboratories and clinical chemistry environments Supporting flow cytometry, cell separation and diagnostics products located at customer sites Your Background – Field Service Engineer, Medical Diagnostic Systems To apply you should be able to demonstrate the following: A strong background working in a field service or technical support role, gained within an electronics or electro-mechanical service or technical support background Applications are welcomed from a wide variety of backgrounds including high value electronics capital equipment,microscopy, cameras, lasers, x-ray security detection, ex-forces (weapons guidance, radar, avionics or biomedical engineering), medical device, biomedical engineering, pathology laboratory diagnostics and laboratory device Qualified to a minimum ONC / HNC level or above in electronics or another relevant technical discipline Impeccable customer service skills and the ability to remain confident in customer facing environments The Company - Field Service Engineer, Medical Diagnostic Systems Instantly recognisable brand leader supplying a wide range of innovative diagnostic based laboratory and medical systems to the healthcare sector Their commitment to investment in Research and Development is second to none in their industry, ensuring that they remain a market leader At the core of their business lie product innovation, excellent customer service and good people This vacancy is being advertised by TRS Consulting. The services advertised by TRS Consulting are those of an employment agency and / or an employment business

Stringent compliance aligned with Medical Device Regulation (MDR)/ Food and Drug Administration (FDA). Overseas Medical Device Compliance,.

They design and manufacture advanced equipment used in research and medical laboratory environments worldwide. Experience supporting technical, laboratory or medical equipment (desirable).

Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity / expression, national origin / ancestry, age, mental / physical disability, medical condition, marital status, veteran status,

A leading tech company in healthcare seeks an experienced professional to assess and certify innovative medical device software. Join us to play a pivotal role in the development and regulation of groundbreaking medical devices.

A leading pharmaceutical company in Cambridge is seeking a qualified professional to oversee project leadership for combination products and standalone medical devices.

A leading medical device company is seeking a Med Device Sales Manager to cover the West Midlands and Trent regions.

A leading healthcare technology company is seeking a Territory Manager to enhance sales of medical devices and maintain customer relations.

The role involves inspecting, testing, and ensuring the compliance of medical devices in clinical settings, with flexibility for full-time or part-time work. Candidates should have experience in working with medical devices and a relevant technical qualification.

A Medical Device company are seeking multiple Technicians to join them on a temporary basis to assist with Validation of a Lateral Flow Device. Ideally some prior experience in a similar environment working with - lateral flow devices, immunoassays , or validation studies of Medical Devices. Medical

Candidates should have over 5 years of sales experience, particularly in healthcare or medical devices, and must excel in communication and relationship-building skills.

A leading medical device company in Greater London is seeking a skilled sales representative to manage product sales and customer engagement. The role requires a minimum of a BA/BS degree and prior experience in the medical device sector.

Minimum of 5 – 8 years packaging development experience – medical devices packaging preferred, certification is desirable. Working knowledge of ISO 13485 and BS EN ISO 11607, and associated global standards, and requirements associated with medical device packaging. Working knowledge of device s

The Veeva MedTech Team is looking for an experienced Account Partner to drive sales for Veeva’s Quality Cloud offerings within Global & Enterprise customers and prospects for Medical Devices & Diagnostics. QMS processes, document management, validation) within the Medical Device & Diagnostics Indu

Candidates should have over 5 years of experience in the medical device industry and familiarity with cybersecurity compliance. The role focuses on ensuring security in medical devices, utilizing various security frameworks, and collaborating with cross-disciplinary teams.

Interest in medical devices and enthusiasm to develop a career in medical sales. Medical Device Sales Representative – South UK Territory. Junior Medical Devices Representative.

We are seeking engineers with SaMD (Software as a Medical device) in technical capacity which can include product design, development and/or testing. Perform unannounced visits to medical device manufacturers globally as a technical expert to check on compliance with certification. Software Medical

The ideal candidate has experience in manufacturing management within regulated environments, ideally in the medical devices or biotech sector. A pioneering medical device company in Oxford is seeking a Senior Manufacturing Manager to lead all manufacturing operations and support rapid growth.

A cutting-edge healthcare technology company is seeking a Mechanical Design Engineer II to join their design team in Greater London.This role involves supporting mechanical design activities throughout the product lifecycle, solving complex engineering challenges, and collaborating with various team

Candidates must have a degree in a scientific discipline, practical validation experience in the Medical Device or Pharmaceutical industry, and strong analytical skills. The position offers a hybrid working model and great employee benefits including 25 days of holiday, an excellent pension plan, an

The process of taking on board software development will be gradual, and supported by current (external) developers, so immediate familiarity with the entire stack isn't expected; however, a strong understanding of embedded development, and prior experience of developing software for medical devices

A global health technology company in Bedford is seeking a Project Manager to lead multi-functional product development projects.The role involves directing project teams, managing budgets from $5 million to $10 million, and ensuring compliance with design control practices.Candidates should have at

A healthcare trust in Greater London is seeking a registered healthcare professional for the Medical Device Training Team. The ideal candidate will be passionate about quality care and possess strong experience in medical device use. This role involves teaching staff on the safe use of medical equip

The successful candidate will have a background in engineering and will be responsible for preventative maintenance, servicing, and repair of medical equipment, ensuring high safety standards.

A leading scientific organization is looking for a Medical Device Lab Technician in the UK. This temporary full-time position offers an opportunity to gain experience in laboratory tests, particularly in validating a lateral flow device.

A leading consulting firm in Greater London seeks a Cybersecurity Consultant with over 5 years of experience in the medical device space.

Med Device Sales Manager JobSalary - £50,000 to £53,000. If this Med Device Sales Manager Job is not quite right for you but you're interested in other opportunities, take a look at our other science jobs.

We seek a Senior QA/RA Engineer focused on software quality assurance and regulatory compliance for medical devices. Experience in QA/RA for medical device software or related fields. Senior QA Engineer - Medical Device Software.

If you are a driven, people-focused medical device sales professional with a positive attitude, ready to take on a broad territory and help shape the future of maternity care, we would love to hear from you. Medical Device Sales Specialist – Maternity & Women’s Health. We are seeking an ambitiou

A growing medical device organization in London seeks an experienced Quality / Manufacturing Engineer to join their team. This on-site role focuses on ensuring product quality and compliance with regulations in the manufacturing of high-risk medical devices. Candidates should have a strong backgroun

The Quality Team's goal is to ensure full compliance and operational excellence—both within Scarlet and for Medical Device Manufacturers. Work experience - Experience auditing against medical device quality management requirements (e. Scarlet’s Quality Team plays a pivotal role in ensuring that

A leading medical device company in Greater London is seeking a skilled Customer/Field Service Engineer to deliver maintenance, installation, and servicing of high voltage medical equipment. This position is ideal for proactive individuals looking to advance their careers in the medical field.

A leading medical technology company is looking for a motivated Junior Medical Devices Representative to support sales and customer engagement across the London - South UK territory. Ideal candidates should have a degree in a relevant field, a keen interest in medical sales, and strong communication

Key Account Manager - Medical Device. Key Account Manager - Medical Device.

Position: Director at Medtech Search Associates - Specialist Medical Device Sales Recruiter and Headhunter. Are you a Physiotherapist interested in transitioning into medical device sales? This could be your IDEAL job. Sign in to set job alerts for “Medical Device Sales Specialist” roles.

A leading medical technology company is looking for a Technical Support Helpdesk Representative to provide essential support for medical devices.

Scarlet is the pre-eminent authority on AI medical devices. Scarlet’s Quality Team plays a pivotal role in ensuring that Medical Device Manufacturers meet and exceed the Quality Management System (QMS) requirements laid out by the regulators. The Quality Team's goal is to ensure full compliance an