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📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...

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📑 ​RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. ✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member state ...

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📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...

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📑 The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics.Responsibilities include but are not limited to:* Ensuring studies are conducted and documented in accordance with the study protocol, standard operating ...

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📑 The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics.Responsibilities include but are not limited to:* Ensuring studies are conducted and documented in accordance with the study protocol, standard operating ...

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📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...

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📑 Great that you're thinking about a career with BSI! Job Title: Regulatory Lead(IVD) Reports to: Head of Notified Body IVDR Location: EU / UK - homebased Overview / Purpose of the position: Provide regulatory support to the Head of NB IVDR in the establishment and maint ...

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📑 IVD Regulatory Affairs Specialist | Remote | EU Proclinical are seeking a dedicated professional to lead regulatory affairs in the in-vitro diagnostics sector within the EU for a Regulatory Specialist role which is a remote position. Responsibilities: - Independently assemble and maintain technical and regulatory documentation for EU Annex XIV ...

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📑 The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Responsibilities include but are not limited to:* Ensuring studies are conducted and documented in accordance with the study protocol, standard operating ...

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📑 The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Responsibilities include but are not limited to:* Ensuring studies are conducted and documented in accordance with the study protocol, standard operating ...

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📑 The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Responsibilities include but are not limited to:* Ensuring studies are conducted and documented in accordance with the study protocol, standard operating ...

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📑 The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Responsibilities include but are not limited to:* Ensuring studies are conducted and documented in accordance with the study protocol, standard operating ...

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📑 IVD Regulatory Affairs Specialist | Remote | EU Proclinical are seeking a dedicated professional to lead regulatory affairs in the in-vitro diagnostics sector within the EU for a Regulatory Specialist role which is a remote position. Responsibilities: - Independently assemble and maintain technical and regulatory docume ...

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📑 Oxford Global Resources is hiring a Clinical Study Lead (IVD experience is a must) for temporary maternity leave. As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols, investigator brochure, informed consent, contracts, and reports, in compliance w ...

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📑 Oxford Global Resources is hiring a Clinical Study Lead (IVD experience is a must) for temporary maternity leave. As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols, investigator brochure, informed consent, contracts, and reports, in compliance w ...

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📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...

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📑 BioTalent have partnered with a diagnostic services leader, on their search for a IVD and Clinical Pathology Business Development Manager, based in the UK. As a Business Development Manager focusing on IVD/Clinical Pathology and Genetics, you'll be instrumental in driving sales and expanding their client base across the UK (This role requires 60% t ...

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📑 BioTalent have partnered with a diagnostic services leader, on their search for a IVD and Clinical Pathology Business Development Manager, based in the UK. As a Business Development Manager focusing on IVD/Clinical Pathology and Genetics, you'll be instrumental in driving sales and expanding their client base across the UK (This role requires 60% t ...

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📑 ​RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. ✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states within the ...

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📑 ​RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. ✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states w ...

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📑 Responsibilities Acts as a product and business owner for LC-MS/MS instrument solutions specific for clinical diagnostics and therapeutic areas. Be responsible for the VoC and competitive benchmark efforts to identify unmet need and develop value proposition of new product solutions for key therapeutic areas of responsibility. Lead the ...

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📑 REGULATORY AFFAIRS OFFICER BIOTECHNOLOGY LIFE SCIENCES MEDICAL DEVICES OR PHARMACEUTICALS BASED EDINBURGH – SALARY EXCELLENT PLUS BENEFITS / HYBRID WORKING Based in Edinburgh, ESS's client is a well-established bio-manufacturing organisation, with an internationally recognised product portfolio. The product range includes in vi ...

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📑 REGULATORY AFFAIRS OFFICER BIOTECHNOLOGY LIFE SCIENCES MEDICAL DEVICES OR PHARMACEUTICALS BASED EDINBURGH – SALARY EXCELLENT PLUS BENEFITS / HYBRID WORKING Based in Edinburgh, ESS's client is a well-established bio-manufacturing organisation, with an internationally recognised product portfolio. The product range includes in vi ...

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📑 Overview Job Title: Regulatory Affairs Officer/ Senior Officer Location: Near Edinburgh, Scotland, UK Remuneration: Attractive salary and package An exciting opportunity to join an established and growing IVD manufacturer and support a growing Regulatory Affairs Department. In this role as a Regulatory Affairs Officer/ Senior Offic ...

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📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...

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📑 Responsibilities Acts as a product and business owner for LC-MS/MS instrument solutions specific for clinical diagnostics and therapeutic areas. Be responsible for the VoC and competitive benchmark efforts to identify unmet need and develop value proposition of new product solutions for key therapeutic a ...

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📑 Overview Job Title: Regulatory Affairs Officer/ Senior Officer Location: Near Edinburgh, Scotland, UK Remuneration: Attractive salary and package An exciting opportunity to join an established and growing IVD manufacturer and support a growing Regulatory Affairs Depa ...

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📑 Product Sales Specialist, UK IVD Market (FIT Testing)South Region£35,000 to £45,000 DOESouth RegionCommercial Bonus + Car or Car Allowance + Healthcare + Pension +TrainingMy client, a market leader within their industry is growing and looking for an experienced technical sales professional with a background in Biomedical sciences to ...

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📑 Product Sales Specialist, UK IVD Market (FIT Testing) South Region £35,000 to £45,000 DOE South RegionCommercial Bonus + Car or Car Allowance + Healthcare + Pension +Training My client, a market leader within their industry is growing and looking for an experienced technical sales professional with a background in Biomedical sciences to drive ...

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📑 Overview Senior Regulatory Affairs Officer Hybrid working from Edinburgh office Offering up to £55,000 Per Annum, plus bonus and benefit package CPL Life Sciences has partnered with an organization who has over 30 years history working in the in-vitro diagnostics field. Headquartered in Edinburgh this organization is looking for an exp ...

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📑 Overview Business Development Manager – IVD Glasgow Based with an innovative biotechnology company, this Business Development Manager opportunity is a great role for someone looking to step into a strategic position and drive sales activities on an international level. The organisation specia ...

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📑 Development ScientistBased on the WirralIn-vitro DiagnosticsPermanentAre you a talented scientist with a background in Biochemistry, Bioassays, or Microbiology? Do you thrive on the challenge of developing new methods and working on cutting-edge in vitro diagnostic (IVD) projects? We have the perfect role for you!About t ...

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📑 The Role Ensuring regulatory compliance for existing products Developing regulatory strategies for new products Montior markets for updates and changes to regulations Ensuring the QMS remains updated and adhering to legislation/standards You 2-4 years of professional experience in IVD Regulatory Affairs Experience in re ...

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📑 Overview Senior Regulatory Affairs Officer Hybrid working from Edinburgh office Offering up to £55,000 Per Annum, plus bonus and benefit package CPL Life Sciences has partnered with an organization who has over 30 years history working in the in-vitro diagnostics field. Headquartered in Edin ...

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📑 Stem Recruitment have a couple of opportunities for experienced RA & Senior RA's based near Edinburgh for a medical device company.The roles are responsible for building regulatory strategy, determining applicable regulatory requirements, proposing solutions to comply with regulatory requirements and managing product license registration wi ...

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📑 Stem Recruitment have a couple of opportunities for experienced RA & Senior RA's based near Edinburgh for a medical device company.The roles are responsible for building regulatory strategy, determining applicable regulatory requirements, proposing solutions to comply with regulatory requirements and managing product license registratio ...

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📑 The Role Ensuring regulatory compliance for existing products Developing regulatory strategies for new products Montior markets for updates and changes to regulations Ensuring the QMS remains updated and adhering to legislation/standards < ...

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📑 As part of the certification body (TÜV SÜD BABT), this role will have the key responsibility for the final review and certificate decisions for the UK Approved Body scheme for medical devices.Main Duties and Responsibilities: * Handling of final review and certification of conformity assessment processes according to the UKCA scheme for me ...

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📑 Overview The Senior Project Manager will be part of the PMO and be responsible for supporting program management activities across the Company. This will include delivery of new product development projects for IVD products for infectious disease, automation products to automate clinical testing and corporate projects where appropriate. It ...

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📑 This position is offered as a fixed term contract (FTC) of circa 9 months and is responsible for Global Regulatory activities within Oxford Immunotec (Revvity) Role Description: Overall responsibilities: To assist the Regulatory team with the Company’s regulatory process leading to timely product approval for both new and existing products i ...

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📑 Stem Recruitment are currently looking for an experienced Lead Hardware Support Engineer for a medical device company based near Motherwell. This role will include assisting with troubleshooting, testing, and investigation activities for their IVD instrumentation platform hardware as part of the System Integration Team. Some of the responsibilities ...

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📑 The Senior Project Manager will be part of the PMO and be responsible for supporting program management activities across the Company. This will include delivery of new product development projects for IVD products for infectious disease, automation products to automate clinical testing and corporate projects where appropriate. It is the responsi ...

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📑 Company: Do you want to make a difference while advancing your career? Come join Osler. We are a UK diagnostics company whose purpose is to enable anyone, anywhere, to access, understand, and act on their health, to live healthier, happier, and longer lives. We are realising this through the development of the Osler Or ...

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📑 Overview The Senior Project Manager will be part of the PMO and be responsible for supporting program management activities across the Company. This will include delivery of new product development projects for IVD products for infectious disease, automation products to automate clinical testing and corporate projects ...

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📑 This position is offered as a fixed term contract (FTC) of circa 9 months and is responsible for Global Regulatory activities within Oxford Immunotec (Revvity) Role Description: Overall responsibilities: To assist the Regulatory team with the Company’s regulatory process leading to timely product approval f ...

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📑 Cure Talent are delighted to be partnered with an exciting Diagnostics company, specialising in Gastrointestinal Cancer, who, due to their continued growth, have an exciting opportunity for a Chief Operations Officer to join them.As the new Chief Operations Officer, you will oversee and optimise all operational aspects of the company, worki ...

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📑 Cure Talent are delighted to be partnered with an exciting Diagnostics company, specialising in Gastrointestinal Cancer, who, due to their continued growth, have an exciting opportunity for a Chief Operations Officer to join them.As the new Chief Operations Officer, you will oversee and optimise all operational aspects of the company, worki ...

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📑 Our client is a US-headquartered multinational medical device business with a market-leading presence across multiple healthcare disciplines. The business runs in a state of perpetual innovation, continually developing new technologies and enhancing the patient experience. Due to their continued growth, they are now looking for a Regulatory ...

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📑 Our client is a US-headquartered multinational medical device business with a market-leading presence across multiple healthcare disciplines. The business runs in a state of perpetual innovation, continually developing new technologies and enhancing the patient experience. Due to their continued growth, they are now looking for a Regulatory Affai ...

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📑 : The Global Portfolio Life Cycle Leader, Multiple Myeloma Diagnostic Innovations, will lead, define and implement the company’s marketing strategy on this major strategic pillar for the Protein Diagnostics Division (PDX). The company’s ambition is to bring earlier and better diagnosis of Multiple Myeloma to more patients and improv ...

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