Join Our Team as a Medical Devices Clinical Safety Team Member! Are you passionate about improving patient safety and clinical outcomes? Do you want to make a real difference in the medical devices industry? If so, we have an exciting opportunity for you! Position: Medical Devices Clinical Safety Team Member Location: Hybrid/Remote Contract Type: Fixed Term Contract (12 months) Working Pattern: Full Time - Outside IR35 Why Join Us? At our company, we believe in fostering a vibrant and collaborative workplace where your contributions matter. As a Medical Devices Clinical Safety Team Member, you will play a crucial role in ensuring the safety and efficacy of our innovative products. What You'll Do: Support Clinical Safety: Collaborate with our clinical teams to assess and monitor the safety of medical devices throughout their life cycle. Data Analysis: analyse clinical data to identify trends, risks, and opportunities for improvement. Report Generation: Prepare and present detailed reports on clinical safety findings to stakeholders. Cross-Functional Collaboration: Work closely with regulatory, quality assurance, and product development teams to ensure compliance and safety. Risk Management: Participate in risk assessment and mitigation activities to uphold patient safety standards. Who You Are: Background in Healthcare: You have a degree in a relevant field (eg, life sciences, nursing) or equivalent experience in clinical safety or medical devices. Analytical Thinker: You possess strong analytical skills with a keen eye for detail. Effective Communicator: You can convey complex information clearly and concisely to various audiences. Team Player: You thrive in a collaborative environment and are excited to work with diverse teams. Proactive Attitude: You take initiative and are eager to contribute to the success of our projects. Why You'll Love Working With Us: Impactful Work: Your efforts will directly contribute to the safety and well-being of patients using our medical devices. Supportive Environment: We value your professional growth and provide opportunities for training and development. Dynamic Team Culture: Join a friendly, motivated team where your ideas and contributions are valued. Competitive Salary & Benefits: Enjoy a comprehensive benefits package that supports your health, well-being, and work-life balance. Ready to Make a Difference? If you are excited about the prospect of joining a forward-thinking company that prioritises patient safety and innovative solutions, we would love to hear from you! Let's work together to shape the future of medical devices and enhance patient safety! Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
17/07/2025
Join Our Team as a Medical Devices Clinical Safety Team Member! Are you passionate about improving patient safety and clinical outcomes? Do you want to make a real difference in the medical devices industry? If so, we have an exciting opportunity for you! Position: Medical Devices Clinical Safety Team Member Location: Hybrid/Remote Contract Type: Fixed Term Contract (12 months) Working Pattern: Full Time - Outside IR35 Why Join Us? At our company, we believe in fostering a vibrant and collaborative workplace where your contributions matter. As a Medical Devices Clinical Safety Team Member, you will play a crucial role in ensuring the safety and efficacy of our innovative products. What You'll Do: Support Clinical Safety: Collaborate with our clinical teams to assess and monitor the safety of medical devices throughout their life cycle. Data Analysis: analyse clinical data to identify trends, risks, and opportunities for improvement. Report Generation: Prepare and present detailed reports on clinical safety findings to stakeholders. Cross-Functional Collaboration: Work closely with regulatory, quality assurance, and product development teams to ensure compliance and safety. Risk Management: Participate in risk assessment and mitigation activities to uphold patient safety standards. Who You Are: Background in Healthcare: You have a degree in a relevant field (eg, life sciences, nursing) or equivalent experience in clinical safety or medical devices. Analytical Thinker: You possess strong analytical skills with a keen eye for detail. Effective Communicator: You can convey complex information clearly and concisely to various audiences. Team Player: You thrive in a collaborative environment and are excited to work with diverse teams. Proactive Attitude: You take initiative and are eager to contribute to the success of our projects. Why You'll Love Working With Us: Impactful Work: Your efforts will directly contribute to the safety and well-being of patients using our medical devices. Supportive Environment: We value your professional growth and provide opportunities for training and development. Dynamic Team Culture: Join a friendly, motivated team where your ideas and contributions are valued. Competitive Salary & Benefits: Enjoy a comprehensive benefits package that supports your health, well-being, and work-life balance. Ready to Make a Difference? If you are excited about the prospect of joining a forward-thinking company that prioritises patient safety and innovative solutions, we would love to hear from you! Let's work together to shape the future of medical devices and enhance patient safety! Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
Scientist Lab Technician Assay Development (m/f/d) - high throughput lab - analyzer/data analyses/biostatistics/BSL2/GMP/GLP/English Project : For our customer Roche Diagnostics International AG based in Rotkreuz we are looking for Scientist Lab Technician Assay Development (m/f/d). Background : The Assay Development team is responsible for the development of molecular diagnostic and screening tests based on PCR technology in the areas of infectious diseases, genomics, and oncology, from early feasibility to commercial launch. Our main areas of responsibility include initial prototyping; optimization of assay design to meet product requirements and ensure manufacturability; development of test methods and acceptance criteria; transfer of reagent manufacturing instructions, test methods, and workflows to Operations; the design and execution of verification and validation activities, including guard-band studies, stability studies, and technical performance verification studies; and documentation of analytical performance for product labeling and regulatory submission packages. Throughout the product development phases, Assay Development interfaces with various departments including Research, Operations, Quality, Regulatory, and Business in order to create and realize what patients need next The perfect candidate : Graduate as Biomedical Analyst Scientist (BMA HF) or apprenticeship as Lab Technician (Biology, Medical Diagnostics, Chemistry) or Bachelor/& Master degree in Life Sciences (no PhD graduates). Min. 2 years of lab working experience (ideally in the Mol. Biology/PCR field) with data analyses and biostatistics. Very good MS Office and documentation skills as well as English fluency. Open-minded and proactive team player Tasks & Responsibilities: * Working with high throughput lab - analyzer * Routine lab work with infectious samples and leading of own experiments including the analysis of them * Plan and execute different work packages for the development of molecular diagnostics test * Participation in project meetings and presentation of experimental data * Precise documentation of experiments using electronic lab journals according to GMP Standards * Equipment handling and maintenance * Statistical data analysis using different software and tools (eg JMP) * Author official documents (eg Design History Files) Must Haves: * Graduate as Biomedical Analyst Scientist (BMA HF) or apprenticeship as Lab Technician (Biology, Medical Diagnostics, Chemistry) or at least Bachelor or Master degree in Life Sciences with practical experience from the Lab (no PhD graduates) * Ideally 2+ years of lab experience with data analyses and biostatistics * Very good and thorough documentation skills * English fluency written and orally is a must, German is a plus * Open-minded team player * Pro-active mindset and organized working style * Flexible, strategic thinking and self-dependent person Nice to Haves: * Lab experience from a biotechnical environment with infectious sample handling Biosafety Level 2 * Experience in a GMP/GLP environment Reference Nr.: 924294SDA Role : Scientist Lab Technician Assay Development (m/f/d) Industrie : Pharma Workplace : Rotkreuz Pensum : 100% Start : ASAP Duration : 12 Deadline : 21.07.2025 If you are interested in this position, please send us your complete dossier via the link in this advertisement. About us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering. We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.
15/07/2025
Contractor
Scientist Lab Technician Assay Development (m/f/d) - high throughput lab - analyzer/data analyses/biostatistics/BSL2/GMP/GLP/English Project : For our customer Roche Diagnostics International AG based in Rotkreuz we are looking for Scientist Lab Technician Assay Development (m/f/d). Background : The Assay Development team is responsible for the development of molecular diagnostic and screening tests based on PCR technology in the areas of infectious diseases, genomics, and oncology, from early feasibility to commercial launch. Our main areas of responsibility include initial prototyping; optimization of assay design to meet product requirements and ensure manufacturability; development of test methods and acceptance criteria; transfer of reagent manufacturing instructions, test methods, and workflows to Operations; the design and execution of verification and validation activities, including guard-band studies, stability studies, and technical performance verification studies; and documentation of analytical performance for product labeling and regulatory submission packages. Throughout the product development phases, Assay Development interfaces with various departments including Research, Operations, Quality, Regulatory, and Business in order to create and realize what patients need next The perfect candidate : Graduate as Biomedical Analyst Scientist (BMA HF) or apprenticeship as Lab Technician (Biology, Medical Diagnostics, Chemistry) or Bachelor/& Master degree in Life Sciences (no PhD graduates). Min. 2 years of lab working experience (ideally in the Mol. Biology/PCR field) with data analyses and biostatistics. Very good MS Office and documentation skills as well as English fluency. Open-minded and proactive team player Tasks & Responsibilities: * Working with high throughput lab - analyzer * Routine lab work with infectious samples and leading of own experiments including the analysis of them * Plan and execute different work packages for the development of molecular diagnostics test * Participation in project meetings and presentation of experimental data * Precise documentation of experiments using electronic lab journals according to GMP Standards * Equipment handling and maintenance * Statistical data analysis using different software and tools (eg JMP) * Author official documents (eg Design History Files) Must Haves: * Graduate as Biomedical Analyst Scientist (BMA HF) or apprenticeship as Lab Technician (Biology, Medical Diagnostics, Chemistry) or at least Bachelor or Master degree in Life Sciences with practical experience from the Lab (no PhD graduates) * Ideally 2+ years of lab experience with data analyses and biostatistics * Very good and thorough documentation skills * English fluency written and orally is a must, German is a plus * Open-minded team player * Pro-active mindset and organized working style * Flexible, strategic thinking and self-dependent person Nice to Haves: * Lab experience from a biotechnical environment with infectious sample handling Biosafety Level 2 * Experience in a GMP/GLP environment Reference Nr.: 924294SDA Role : Scientist Lab Technician Assay Development (m/f/d) Industrie : Pharma Workplace : Rotkreuz Pensum : 100% Start : ASAP Duration : 12 Deadline : 21.07.2025 If you are interested in this position, please send us your complete dossier via the link in this advertisement. About us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering. We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.
This is a fantastic opportunity to work as a Pathologist for a major pharmaceutical company on a remote basis, outside IR35, requiring 20+ hours per week (spread over multiple days). The key experience required for this Pathologist position is: Medical degree Tissue diagnostics Annotations Oncology Image analysis Digital pathology If you do have the relevant experience for these remote Pathologist positins, please do send through your CV.
15/07/2025
Contractor
This is a fantastic opportunity to work as a Pathologist for a major pharmaceutical company on a remote basis, outside IR35, requiring 20+ hours per week (spread over multiple days). The key experience required for this Pathologist position is: Medical degree Tissue diagnostics Annotations Oncology Image analysis Digital pathology If you do have the relevant experience for these remote Pathologist positins, please do send through your CV.
Clinical Research Associate (m/f/d) - clinical research or laboratory research/ICH/GCP/therapeutic and protocol knowledge/MS Office/Pathology/English Project : For our customer Roche Diagnostics International AG based in Rotkreuz we are looking for a Clinical Research Associate (m/f/d). Background: The Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. The perfect cdidate has a degree in Medical technology with first professional experiences in clinical research or laboratory research. Additionally, the person brings basic knowledge of, and skill in applying, applicable clinical research regulatory requirements as well as excellent oral and written communication skills in English. Tasks & Responsibilities: * Ensuring studies are conducted and documented in accordance with the study protocol, standard operating procedures, good clinical practices and other applicable regulatory requirements * Validating product performance claims * Supplying data for critical Regulatory submissions * Defining the functional and clinical utility of investigational products * Obtaining opinions and input regarding investigational products from laboratories or customers, who may be considered key opinion leaders * The CRA is responsible for adhering to the policies of the quality system and achieving quality objectives through daily actions * Performing or coordinating aspects of clinical studies including site selection, study initiation, site monitoring, and study closeout * Maintaining communication with study investigators to ensure studies are completed in a timely fashion and ensuring that study objectives are met * Interfacing with cross functional staff to support post launch activities * Reviewing cases with investigators to resolve discrepancies * Ensuring that studies adhere to FDA regulations, Good Clinical Practices, IVD directives, and Roche policies and procedures. Must Haves : * Bachelor's degree (Masters and PhD also ok) in science or relevant field, Medical technology degree preferred, but not required if R&D background is adequate * Preferably experience in clinical research or laboratory research * Min. 2 years of prior relevant experience * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines) * Excellent oral and written communication skills in English * Excellent planning, organizing, and interpersonal skills * Ability to work independently, make sound decisions, and to analyze and solve problems * Medical laboratory experience preferred * Good therapeutic and protocol knowledge. * Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable) * Organizational and problem-solving skills * Effective time and financial management skills * Ability to establish and maintain effective working relationships with coworkers, managers, and clients Nice to Have: * Experience in Pathology Reference Nr.: 924307SDA Role : Clinical Research Associate (m/f/d) Industrie : Pharma Workplace : Rotkreuz Pensum : 100 % Start : ASAP ( latest Start Date: 01.10.2025) Duration : 12 Deadline : 20.07.2025 If you are interested in this position, please send us your complete dossier via the link in this advertisement. About us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering. We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.
14/07/2025
Contractor
Clinical Research Associate (m/f/d) - clinical research or laboratory research/ICH/GCP/therapeutic and protocol knowledge/MS Office/Pathology/English Project : For our customer Roche Diagnostics International AG based in Rotkreuz we are looking for a Clinical Research Associate (m/f/d). Background: The Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. The perfect cdidate has a degree in Medical technology with first professional experiences in clinical research or laboratory research. Additionally, the person brings basic knowledge of, and skill in applying, applicable clinical research regulatory requirements as well as excellent oral and written communication skills in English. Tasks & Responsibilities: * Ensuring studies are conducted and documented in accordance with the study protocol, standard operating procedures, good clinical practices and other applicable regulatory requirements * Validating product performance claims * Supplying data for critical Regulatory submissions * Defining the functional and clinical utility of investigational products * Obtaining opinions and input regarding investigational products from laboratories or customers, who may be considered key opinion leaders * The CRA is responsible for adhering to the policies of the quality system and achieving quality objectives through daily actions * Performing or coordinating aspects of clinical studies including site selection, study initiation, site monitoring, and study closeout * Maintaining communication with study investigators to ensure studies are completed in a timely fashion and ensuring that study objectives are met * Interfacing with cross functional staff to support post launch activities * Reviewing cases with investigators to resolve discrepancies * Ensuring that studies adhere to FDA regulations, Good Clinical Practices, IVD directives, and Roche policies and procedures. Must Haves : * Bachelor's degree (Masters and PhD also ok) in science or relevant field, Medical technology degree preferred, but not required if R&D background is adequate * Preferably experience in clinical research or laboratory research * Min. 2 years of prior relevant experience * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines) * Excellent oral and written communication skills in English * Excellent planning, organizing, and interpersonal skills * Ability to work independently, make sound decisions, and to analyze and solve problems * Medical laboratory experience preferred * Good therapeutic and protocol knowledge. * Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable) * Organizational and problem-solving skills * Effective time and financial management skills * Ability to establish and maintain effective working relationships with coworkers, managers, and clients Nice to Have: * Experience in Pathology Reference Nr.: 924307SDA Role : Clinical Research Associate (m/f/d) Industrie : Pharma Workplace : Rotkreuz Pensum : 100 % Start : ASAP ( latest Start Date: 01.10.2025) Duration : 12 Deadline : 20.07.2025 If you are interested in this position, please send us your complete dossier via the link in this advertisement. About us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering. We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.
Radfield Home Care is an award-winning leader in the UK home care sector, dedicated to providing exceptional support to older individuals. Our mission is to empower clients by delivering personalized care that helps them stay connected to what matters most in their lives. You must have a driving license for this position. Details; We are seeking a compassionate and dedicated Support Worker to join our team at Radfield Home Care Bath. In this role, you will provide essential support to our clients, helping them maintain their independence and quality of life in the comfort of their own homes. A culture which is welcoming, friendly, supportive and inclusive Fair and competitive hourly rate £14.00 - £21.00 Full time and part time hours available offering 20 - 40 hrs pw PAID travel time at your standard hourly rate Flexible working hours Appreciation & recognition celebrating achievements of individuals & teams PAID Holiday Tax -Free per mile Company Pension Referral Programme up to £500 PAID Induction PAID Training Provided FREE Uniform Flexible Working Hours Progression Opportunities Encouragement to develop your skills and knowledge A great personality and good values are the most important attributes to deliver great care. You will need to be over the age of 18, have a full UK driving licence and access to a vehicle and the right to work in the UK. We invite qualified candidates who are passionate about making a difference in the lives of others to apply for this rewarding opportunity as a Social Worker. This post is exempt from the Rehabilitation of Offenders Act 1974. The role requires contact with vulnerable clients and will be subject to enhanced DBS disclosure and satisfactory references. Responsibilities Assist clients with daily living activities, including personal care, meal preparation, and medication management. Develop and implement individualized care plans tailored to each client's needs. Communicate effectively with clients, families, and healthcare professionals to ensure coordinated care. Provide companionship and emotional support to enhance clients' well-being. Maintain accurate records of client progress and any changes in condition. Support clients in engaging with their community and pursuing interests that matter to them. Requirements Experience in home care or a related field is preferred but not essential. Strong communication skills, both verbal and written, with a good command of English. Ability to develop and follow care plans effectively. A compassionate approach with a genuine desire to help others. A valid driver's license is beneficial for travel between client homes. If you're ready to make a meaningful difference in the lives of others and join a supportive team that values your contributions, apply today at Radfield Home Care! Benefits: Company events Company pension Flexitime On-site parking Referral programme Schedule: Day shift Monday to Friday Evening shift Weekend availability Application question(s): Do you have a Full UK Driving Licence and have access to a vehicle Do you require Sponsorship? Do you live in Bath?
14/07/2025
Full time
Radfield Home Care is an award-winning leader in the UK home care sector, dedicated to providing exceptional support to older individuals. Our mission is to empower clients by delivering personalized care that helps them stay connected to what matters most in their lives. You must have a driving license for this position. Details; We are seeking a compassionate and dedicated Support Worker to join our team at Radfield Home Care Bath. In this role, you will provide essential support to our clients, helping them maintain their independence and quality of life in the comfort of their own homes. A culture which is welcoming, friendly, supportive and inclusive Fair and competitive hourly rate £14.00 - £21.00 Full time and part time hours available offering 20 - 40 hrs pw PAID travel time at your standard hourly rate Flexible working hours Appreciation & recognition celebrating achievements of individuals & teams PAID Holiday Tax -Free per mile Company Pension Referral Programme up to £500 PAID Induction PAID Training Provided FREE Uniform Flexible Working Hours Progression Opportunities Encouragement to develop your skills and knowledge A great personality and good values are the most important attributes to deliver great care. You will need to be over the age of 18, have a full UK driving licence and access to a vehicle and the right to work in the UK. We invite qualified candidates who are passionate about making a difference in the lives of others to apply for this rewarding opportunity as a Social Worker. This post is exempt from the Rehabilitation of Offenders Act 1974. The role requires contact with vulnerable clients and will be subject to enhanced DBS disclosure and satisfactory references. Responsibilities Assist clients with daily living activities, including personal care, meal preparation, and medication management. Develop and implement individualized care plans tailored to each client's needs. Communicate effectively with clients, families, and healthcare professionals to ensure coordinated care. Provide companionship and emotional support to enhance clients' well-being. Maintain accurate records of client progress and any changes in condition. Support clients in engaging with their community and pursuing interests that matter to them. Requirements Experience in home care or a related field is preferred but not essential. Strong communication skills, both verbal and written, with a good command of English. Ability to develop and follow care plans effectively. A compassionate approach with a genuine desire to help others. A valid driver's license is beneficial for travel between client homes. If you're ready to make a meaningful difference in the lives of others and join a supportive team that values your contributions, apply today at Radfield Home Care! Benefits: Company events Company pension Flexitime On-site parking Referral programme Schedule: Day shift Monday to Friday Evening shift Weekend availability Application question(s): Do you have a Full UK Driving Licence and have access to a vehicle Do you require Sponsorship? Do you live in Bath?
Join Our Team Care Support Worker Wanted! Location: Plymouth and surrounding areas Guaranteed Hours: 16 hours per week (with flexible scheduling available) Pay: £13.21 per hour Enhanced Rates: £16.51 per hour (Weekends & Bank Holidays) Mileage: 40p per mile Are you a kind, caring, and reliable individual looking to make a real difference in people s lives? Anchor Point Homecare is looking for compassionate Care Support Workers to join our dedicated team. What We Offer: Guaranteed minimum of 16 hours per week Flexible working hours to suit your lifestyle Paid training no experience needed DBS check covered by us Free uniform provided Supportive and friendly working environment Requirements: Must hold a valid driving licence and have access to your own car Willing to work predominantly in the Plymouth area Passionate about delivering high-quality care If you're ready to take the next step in your care career, we d love to hear from you! Click Apply today Call us:
10/07/2025
Full time
Join Our Team Care Support Worker Wanted! Location: Plymouth and surrounding areas Guaranteed Hours: 16 hours per week (with flexible scheduling available) Pay: £13.21 per hour Enhanced Rates: £16.51 per hour (Weekends & Bank Holidays) Mileage: 40p per mile Are you a kind, caring, and reliable individual looking to make a real difference in people s lives? Anchor Point Homecare is looking for compassionate Care Support Workers to join our dedicated team. What We Offer: Guaranteed minimum of 16 hours per week Flexible working hours to suit your lifestyle Paid training no experience needed DBS check covered by us Free uniform provided Supportive and friendly working environment Requirements: Must hold a valid driving licence and have access to your own car Willing to work predominantly in the Plymouth area Passionate about delivering high-quality care If you're ready to take the next step in your care career, we d love to hear from you! Click Apply today Call us:
RMI Global Solutions
Stoke Gifford, Gloucestershire
About RMI: RMI Global Solutions (Remote Medical International) is a leading provider of bespoke medical, security, and HSE (Health, Safety, and Environment) solutions for operations in complex and remote environments worldwide. With over 20 years of experience, we are dedicated to protecting and saving lives, enabling workers and organisations to thrive in challenging settings. We deliver high-quality, reliable medical support to a diverse range of clients globally, ensuring their teams operate safely and efficiently. The Opportunity: RMI is seeking a highly competent and proactive QNUK Level 3 First Aider to provide essential immediate medical assistance for our valued client's on-site population in the Bristol area. This is a crucial role where you will help ensure the safety and well-being of individuals at our client's premises. The successful candidate will be provided with all necessary equipment and a dedicated vehicle for exclusive use on the client's site. RMI is a member of the Armed Forces Covenant and encourages those from all military backgrounds to apply. Key Responsibilities: Respond promptly and effectively to all requests for first aid assistance for injuries and illnesses occurring on the client's site. Conduct initial assessments of casualties, prioritising needs and taking appropriate action in accordance with QNUK Level 3 First Aid at Work (or equivalent) training. Administer emergency first aid treatments for a wide range of conditions, including but not limited to: Unresponsive casualties (CPR, recovery position) Choking External bleeding (major and minor) Shock Minor injuries (cuts, grazes, bruises, burns, splinters) Suspected head, spinal, and chest injuries Eye injuries Anaphylaxis Major illnesses (e.g., heart attack, stroke, seizures, asthma attacks, diabetic emergencies) Please note: This role does not involve the administration of medication. The primary focus is on immediate first aid response and stabilisation prior to the arrival of professional medical services if required. Ensure all first aid equipment, including the on-site vehicle, is well-maintained, fully stocked, and ready for immediate use. Maintain accurate records of all incidents, assessments, and treatments provided, ensuring confidentiality and adherence to data protection regulations and client-specific protocols. Liaise with emergency services (e.g., paramedics, ambulance) as required, providing clear and concise information. Provide reassurance and support to casualties and those affected by incidents. Adhere strictly to all RMI company policies, the client's site-specific health and safety regulations, and first aid best practices, including infection control. Contribute to a positive and safe working environment, acting as a key medical point of contact on behalf of RMI. Essential Skills & Qualifications: Hold a current QNUK Level 3 Award in First Aid at Work (RQF) or an equivalent, nationally recognised, valid first aid qualification. Proven experience as a First Aider, confidently managing a variety of medical emergencies and injuries. Full, clean UK Driving Licence. Must reside locally or within daily commutable distance to the Bristol (BS34 postcode) area. Strong communication and interpersonal skills, with the ability to remain calm and effective under pressure, and to interact professionally with the client's staff. Excellent observational skills and attention to detail. Ability to work independently and as part of a wider team. Due to the nature of the working environment, the successful candidate must currently hold an Enhanced DBS check, or be willing to undergo and successfully pass an Enhanced DBS check, prior to commencing employment. This role requires the successful candidate to have a current BPSS (security clearance). The successful candidate must be able to provide this or be willing to undergo a BPSS before commencing employment. Proficiency in Microsoft Office applications, and general computer & technology literacy Knowledge of Health and Safety practices. Ability to read, write, speak and comprehend instructions, correspondence and memos in English Must be physically fit to perform job-related tasks. Reasonable accommodations may be made to enable individuals to perform essential functions Desirable Skills: Previous experience in an on-site, industrial, or complex client-facing environment. Additional relevant medical or emergency response qualifications. What We Offer: A competitive salary c£25k The opportunity to be part of a globally recognised organisation with a strong commitment to health and safety. All necessary equipment and a vehicle provided for on-site duties. A stimulating and varied working environment, directly supporting a key RMI client. Holiday entitlement of 20 days plus UK bank holidays
30/06/2025
Seasonal
About RMI: RMI Global Solutions (Remote Medical International) is a leading provider of bespoke medical, security, and HSE (Health, Safety, and Environment) solutions for operations in complex and remote environments worldwide. With over 20 years of experience, we are dedicated to protecting and saving lives, enabling workers and organisations to thrive in challenging settings. We deliver high-quality, reliable medical support to a diverse range of clients globally, ensuring their teams operate safely and efficiently. The Opportunity: RMI is seeking a highly competent and proactive QNUK Level 3 First Aider to provide essential immediate medical assistance for our valued client's on-site population in the Bristol area. This is a crucial role where you will help ensure the safety and well-being of individuals at our client's premises. The successful candidate will be provided with all necessary equipment and a dedicated vehicle for exclusive use on the client's site. RMI is a member of the Armed Forces Covenant and encourages those from all military backgrounds to apply. Key Responsibilities: Respond promptly and effectively to all requests for first aid assistance for injuries and illnesses occurring on the client's site. Conduct initial assessments of casualties, prioritising needs and taking appropriate action in accordance with QNUK Level 3 First Aid at Work (or equivalent) training. Administer emergency first aid treatments for a wide range of conditions, including but not limited to: Unresponsive casualties (CPR, recovery position) Choking External bleeding (major and minor) Shock Minor injuries (cuts, grazes, bruises, burns, splinters) Suspected head, spinal, and chest injuries Eye injuries Anaphylaxis Major illnesses (e.g., heart attack, stroke, seizures, asthma attacks, diabetic emergencies) Please note: This role does not involve the administration of medication. The primary focus is on immediate first aid response and stabilisation prior to the arrival of professional medical services if required. Ensure all first aid equipment, including the on-site vehicle, is well-maintained, fully stocked, and ready for immediate use. Maintain accurate records of all incidents, assessments, and treatments provided, ensuring confidentiality and adherence to data protection regulations and client-specific protocols. Liaise with emergency services (e.g., paramedics, ambulance) as required, providing clear and concise information. Provide reassurance and support to casualties and those affected by incidents. Adhere strictly to all RMI company policies, the client's site-specific health and safety regulations, and first aid best practices, including infection control. Contribute to a positive and safe working environment, acting as a key medical point of contact on behalf of RMI. Essential Skills & Qualifications: Hold a current QNUK Level 3 Award in First Aid at Work (RQF) or an equivalent, nationally recognised, valid first aid qualification. Proven experience as a First Aider, confidently managing a variety of medical emergencies and injuries. Full, clean UK Driving Licence. Must reside locally or within daily commutable distance to the Bristol (BS34 postcode) area. Strong communication and interpersonal skills, with the ability to remain calm and effective under pressure, and to interact professionally with the client's staff. Excellent observational skills and attention to detail. Ability to work independently and as part of a wider team. Due to the nature of the working environment, the successful candidate must currently hold an Enhanced DBS check, or be willing to undergo and successfully pass an Enhanced DBS check, prior to commencing employment. This role requires the successful candidate to have a current BPSS (security clearance). The successful candidate must be able to provide this or be willing to undergo a BPSS before commencing employment. Proficiency in Microsoft Office applications, and general computer & technology literacy Knowledge of Health and Safety practices. Ability to read, write, speak and comprehend instructions, correspondence and memos in English Must be physically fit to perform job-related tasks. Reasonable accommodations may be made to enable individuals to perform essential functions Desirable Skills: Previous experience in an on-site, industrial, or complex client-facing environment. Additional relevant medical or emergency response qualifications. What We Offer: A competitive salary c£25k The opportunity to be part of a globally recognised organisation with a strong commitment to health and safety. All necessary equipment and a vehicle provided for on-site duties. A stimulating and varied working environment, directly supporting a key RMI client. Holiday entitlement of 20 days plus UK bank holidays
