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📑 Senior Incident Response ConsultantSalary: £70-£80k + Bonus + BenefitsLocation: UK Wide - HybridCurrently working with one of the fastest growing MDR firms in the UK who are looking for an Incident Response Lead to help spearhead the function into a best in call cyber detection, monitoring and response function.Gaining access to some of the highest ...

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📑 Senior Incident Response ConsultantSalary: £70-£80k + Bonus + BenefitsLocation: UK Wide - HybridCurrently working with one of the fastest growing MDR firms in the UK who are looking for an Incident Response Lead to help spearhead the function into a best in call cyber detection, monitoring and response function.Gaining access to some of the highest ...

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📑 Senior/Principal EU Regulatory Consultant - RemoteNAMSA pioneered the industry and was the first independent company in the world to focus solely on Medical Device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.We are shaping the industry. NAMSA has b ...

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📑 Senior/Principal EU Regulatory Consultant - RemoteNAMSA pioneered the industry and was the first independent company in the world to focus solely on Medical Device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.We are shaping the industry. NAMSA has b ...

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📑 JOB TITLE : Senior Regulatory Affairs Specialist LOCATION : Remote/Hybrid WORKING HOURS : 37.5 Hours, Monday to Friday A brighter future awaits you At CooperVision, we are proud to be the global leader in contact lenses. At our innovative sites worldwide, we manufacture and distri ...

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📑 The Role This is an exciting opportunity for someone develop their career in Quality Assurance in a market leading, global medical devices company. You’ll be responsible for supporting the compliance team to ensure all required certification is maintained. Complete internal audits in compliance with relevant ...

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📑 Our client is a leading manufacturer of their product range globally and they are looking to employ an additional integral person within their planning team.Main duties will include? Providing the support with generating documentation relating to the technical fil for regulatory submission of their product range? Managing product timelines and proj ...

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📑 Job Description Job Title: Trainee Medical Device Lead Auditor Job Type: Permanent Hours: hours per week Job Location: Field-based (UK, South Region) Travel: Within the UK, a Company car or car allowance provided At SGS, we ...

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📑 Job Description Job Title: Medical Device Lead Auditor Job Type: Permanent Hours: hours per week Job Location: Field-based (UK, South Region) Travel: Within the UK, a Company car or car allowance provided Salary: F ...

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📑 Microsoft Cyber Security Pre Sales ConsultantSalary:- £65-75k + £8k Bonus + Bens dep on Skillset Location:- Central London, 3 days office, 2 days homeEnvironment:- Microsoft Security, Modern Workplace, SIEM, MDR/EDR, M365 Security, Sentinel, Endpoint, Defender, InTune, Windows CoPilot, SharePoint, Lan, Wan, SD-Wan, SASE, Wireless, Firewalls, Audits ...

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📑 Microsoft Cyber Security Pre Sales ConsultantSalary:- £65-75k + £8k Bonus + Bens dep on Skillset Location:- Central London, 3 days office, 2 days homeEnvironment:- Microsoft Security, Modern Workplace, SIEM, MDR/EDR, M365 Security, Sentinel, Endpoint, Defender, InTune, Windows CoPilot, SharePoint, Lan, Wan, SD-Wan, SASE, Wireless, Firewalls, Audits ...

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📑 Role Summary As a Threat Analyst - Tier II on our Managed Detection and Response (MDR) team, you will provide best-in-class monitoring, detection, and response services to proactively defend customer environments before attacks prevail. You will work alongside and contribute to a team of cyber threat hunters, incident resp ...

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📑 We have partnered with a Medical Device manufacturer who are looking to expand their medical writing team with the addition of 2 clinical evaluation focused medical writersPerm opportunity, fully remote, NO SPONSORSHIP AVAILABLE.Duties:- Writer and work on CEPs, CERs, and PMCFs.- Work on clinical performance document ...

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📑 Regulatory Affairs Custom Device Team Lead / Senior Regulatory Affairs Custom Device AssociateMain Purpose of Job and Objectives:Perform Regulatory tasks to ensure compliance with regulations.Prepare regulatory documentation and submissions for product approvals.Develop regulatory plans/strategies for new products and changes to existing products.P ...

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📑 Regulatory Affairs Custom Device Team Lead / Senior Regulatory Affairs Custom Device AssociateMain Purpose of Job and Objectives:Perform Regulatory tasks to ensure compliance with regulations.Prepare regulatory documentation and submissions for product approvals.Develop regulatory plans/strategies for new products and changes to existing products.P ...

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📑 THE RITZ LONDON OVERVIEWLocated between the bustling Piccadilly and the calm oasis of Green Park, TheRitz London hotel offers the height of opulence with luxurious bedrooms,Michelin star dining and world-renowned Afternoon Tea. At every opportunity,our employees create a posi ...

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📑 Conceived by famous hotelier César Ritz in May 1906, with the aim of becoming the ultimate destination for guests looking to stay at the most luxurious hotel in the land, no expense was spared on its opulent interiors and lavish furnishings. Located between the bustling Piccadilly and the calm oasis of Green Park, The Ritz offers the height of opul ...

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📑 JOB TITLE : Senior R&D Quality Engineer LOCATION : Chandlers Ford. Eastleigh WORKING HOURS : Monday to Friday 8.30am to 4.30pm – minimum 3 days office vs 2 days home depending on business need A brighter future awaits you At CooperVision, we are proud to be the global leader in c ...

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📑 Job Description As a Product Assessor , you will play a crucial role in performing assessments on dental products and reviewing technical documentation in strict accordance with the European Medical Device Regulation (EU MDR 2017/745) and the UK Medical Device Regulation (UK MDR 2002) for Class IIa/IIb ...

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📑 QMS for Medical Devices and cutting-edge technologies, you will have a vital role in ensuring the efficient establishment and upkeep of the Quality Management System (QMS) throughout the organisation. This position involves overseeing all aspects of quality management, including adherence to relevant regulations and standards. Key Responsibilit ...

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📑 QMS for Medical Devices and cutting-edge technologies, you will have a vital role in ensuring the efficient establishment and upkeep of the Quality Management System (QMS) throughout the organisation. This position involves overseeing all aspects of quality management, including adherence to relevant regulations and standards. Key Responsibilities ...

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📑 The Role As the Regulatory Affairs Specialist, you will be responsible for; Creating technical files for a range of medical devices, both new and existing devices Perform gap analysis and revision of existing documentation to ensure compliance with MDR Respond to and internal or external regulatory affairs queries You As the Regul ...

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📑 Great that you're thinking about a career with BSI! Excited to grow your career? Our people make all the difference in our success. BSI is a designated European Notified Body, an accredited ISO 13485-certification body, a recognized Auditing Organization under MDSAP, and we have an opportunity for you to join our growing ...

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📑 Regulatory Compliance AssociateI am recruiting on a permanent basis in the Yorkshire region for a Regulatory Compliance Associate to work within a healthcare business. Responding to market opportunity and business requirements within online and regulated sectors.You will be responsible for: * * Responsible f ...

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📑 Regulatory Compliance AssociateI am recruiting on a permanent basis in the Yorkshire region for a Regulatory Compliance Associate to work within a healthcare business. Responding to market opportunity and business requirements within online and regulated sectors.You will be responsible for: * * Responsible f ...

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📑 SOC Analyst – UK/Remote - £40k-45K + BonusMUST HAVE FULL RIGHT TO WORK IN THE UK *SPONSORSHIP NOT AVAILABLE*A growing MSP is looking for an experienced SOC Analyst who wants to work in a team where cyber security is the heart of everything they do!In this team, you will monitor networks and systems, detect security threats, analyse and assess alert ...

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📑 The Role As the Regulatory Affairs Specialist, you will be responsible for; Creating technical files for a range of medical devices, both new and existing devices Perform gap analysis and revision of existing documentation to ensure compliance with MDR Respond to and internal or external ...

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📑 FULL-STACK DEVELOPER – UP TO £70,000. PERMANENT, HYBRID.Cyber Security MDR & PS ConsultancyMage Global’s Co-Founder, Seb, has been partnering with this Managed Detection & Response (MDR) & Cyber Professional Services Consultancy in Chichester, West Sussex.We have had a working relationship over the past year, and ...

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📑 Our client, a dynamic and rapidly evolving Managed Security Services Provider (MSSP), has undergone a strategic transformation, propelling them into the realm of Everything as a Service (XaaS).With an expanded suite of offerings including Software as a Service (SaaS) and Platform as a Service (PaaS), they stand at the forefront of innovation in cyb ...

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📑 Our client, a dynamic and rapidly evolving Managed Security Services Provider (MSSP), has undergone a strategic transformation, propelling them into the realm of Everything as a Service (XaaS).With an expanded suite of offerings including Software as a Service (SaaS) and Platform as a Service (PaaS), they stand at the forefront of innovation in cyb ...

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📑 Great that you're thinking about a career with BSI! About the role: Are you a Microbiologist, Sterilisation Engineer, or Quality Manager looking for an interesting career change? Then this could be the opportunity for you! Here at BSI we hire qualified and experienced industry microbiologists to help clients nav ...

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📑 **Contract Type:** 12 month Fixed Term Contract **Location** : Remote / Hybrid working from our Farnborough office As the Field Actions Lead, you will be a key representative in strategy planning of Field Safety Corrective Actions (FSCA / Correction & Removals) representing the International Markets. You will actively take part in ...

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📑 Our client is looking to recruit an experienced Senior Cloud and Server Technician to join their hugely successful growing team. You will have proven experience supporting Microsoft Networks and Microsoft Cloud Services. You will enjoy working in IT and working for a company with great career development opportunities.Package:Salary of £32k - £44k ...

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