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Medical Writer - Sheffield Are you a skilled medical writer with a passion for regulatory affairs Were on the lookout for talented individuals to join our esteemed regulatory writing team in the UK!...
IVD Scientist Location: Deeside Industrial Estate Salary: £22,000 - £30,000 depending on experience (various bands available) Type: Permanent Hours: Days Monday - Friday RTG is working...
Stem Recruitment have a fantastic opportunity for a Quality Risk Coordinator based in Edinburgh with hybrid working for a medical device company. This person will be responsible for managing Product r...
AuditingRiskStem Recruitment have a fantastic opportunity for a Quality Risk Coordinator based in Edinburgh with hybrid working for a medical device company. This person will be responsible for managing Product r...
riskivdrProgramme Manager - Glasgow - Hybrid A Programme Manager role that is all about saving lives and making a difference in the world through technology! Are you ready to lead complex clinical studies a...
Director, Safety - Medical Device Vigilance Expert page is loaded Director, Safety - Medical Device Vigilance Expert Apply locations United Kingdom - Cambridge time type Full time posted on P...
Were looking for a talented Regulatory Affairs Officer to join the team of a privately owned manufacturer of medical products. In this role, youll audit, report and remedy against standards laid down...
A rapidly growing company who are a leading provider of diagnostic soloutions worldwide, are looking to grow their team. Your new company A rapidly growing diagnostic company who ar...
GLPIVDlaboratorymedicalScientistdevelopmentresearchFISHdiagnosticslaboxfordOxfordshireclinical diagnosticsCambridgeshirebiotechdevicegenomicFFPEOur client, a rapidly growing medical device consultancy are looking for a Regulatory Affairs Consultant to join their team. They provide consulting services to start-ups and small to medium- sized me...
Regulatory AffairsRisk ManagementISO 13485Medical DeviceRemoteCEROur client operates in the Medical Devices business sector and the successful candidate will need to work within this regulatory framework in the Technical Department. The Project Manager will be resp...
Medical DevicesPlasticsProject Management ToolsRegulatory Affairs Consultant - (Medical Devices) Our client, a rapidly growing medical device consultancy are looking for a Senior Regulatory Affairs Consultant to join their team. ...
AuditClinicalMedical DevicesRegulatory AffairsMDRISO 13485MDDUKCAMDSAPIVDRRegulatory Affairs Specialist (medical devices) Our Client a medical device company that operate in the UK and distribute globally are currently hiring for their site in Scotland. T...
Medical DevicesPharmaceuticalRegulatory AffairsIVDTechnical FilesISO 13485SubmissionsRA Manager This prestigious, leading, and well-established medical diagnostic company comprises two flagship business divisions that specialise in the design, manufacture and contin...
ManagementMedical DevicesRegulatory AffairsISO ProceduresIVDQA/ RA Associate Director This prestigious, leading, and well-established medical diagnostic company comprises two flagship business divisions that specialise in the design, manufact...
Quality AssuranceQuality ManagementRegulatory AffairsIVDMHRACK Group are recruiting for a QA and RA Associate Director to join a leading medical diagnostics company at their site based in Gateshead on a permanent full-time basis. The Company:...
CK Group are recruiting for a deputy QA / RA Manager on behalf of a well-established medical diagnostic company, to be based at both of their sites in Gateshead and Sunderland on a permanent basis. <...
Quality & Regulatory Manager TEC Partners are pleased to be recruiting a Quality & Regulatory Manager for a high growth digital in-vitro diagnostics start-up to join their expanding...
IVDTechnical FilesISO 13485Quality Management SystemsCE MarkingSenior IVD Scientist | Newcastle Upon Tyne | £30,000 to £60,000 Our client is a biotechnology company based in the heart of Newcastle City centre who is looking to hire a S...
Assay DevelopmentBiologyClinicalClinical ResearchIVDClinical Study Manager | Newcastle Upon Tyne | £40,000 to £55,000 The Clinical Study Manager will be responsible for management of multiple studies including the planning, ...
Clinic ManagementClinicalStudy ManagersManagerQuality Assurance/ Regulatory Affairs Manager, Medical Devices Location: Liverpool/ site based Type: Permanent Hours: (Monday - F...
Our client is a global medical device company developing and marketing smart connected diagnostics and IVDs. The company has major operations in the UK and internationally and is experiencing rapid gr...
AuditManufacturingRisk ManagementIVDISO 13485quality assurancemedical deviceAssayRisk Specialist Would you like to be part of an organisation which is committed to improving patient lives worldwide through education, collaboration and innovation Do you want to ...
Quality ManagementRisk AssessmentsRisk ManagementOur client is a global medical device company developing and marketing smart connected diagnostics and IVDs. The company has major operations in the UK and internationally and is experiencing rapid gr...
Risk ManagementIVDmanagerquality assuranceISO13485medical deviceAssayFDA 21CFR Part 820IVDRAdecco Life Sciences are proud to be working with a diagnostics company that are looking for a Regulatory Affairs Manager to join the team on a permanent basis. As they progress to commercialisation...
ManagementRegulatoryRegulatory AffairsIVDRegulatory Affairs ManagerRegulatory ManagerIVDRAdecco Life Sciences are excited to have partnered with a leading Diagnostic business looking for a Quality and Regulatory Director to join the team on a permanent basis. You will be providing leade...
RegulatoryIVDDirectorQualityQMSleadershipsubmissionIVDRWe are currently recruiting for a Regulatory Affairs Specialist to join our client in the Medical Device sector on a full-time permanent basis in Newcastle. This role can pay a top ro...
TEC Partners are recruiting for a high-growth, digital in-vitro diagnostic start-up who are looking for a Head of Product to join their expanding team in Cambridge. You will be responsible for transit...
Production Scientist: TEC Partners are pleased to be recruiting a Production Scientist for a high growth digital in-vitro diagnostics start-up to join their expanding team following ...
This role is for a high-growth, digital health medical device start-up company who are looking for a Quality Manager to join their expanding team. They are currently working on an in-vitro diagnostic ...
As a Quality Lead for site and network complex projects you will be ensuring compliance is considered through all project phases, generate Quality plans, Lead Risk Assessments and Change controls.
Are you a Regulatory Affairs Specialist looking for a new exciting job opportunity We are currently looking for a Regulatory Affairs Specialist to join a leading diagnostics company based in the Manc...
Support regulatory activities involving IVD medical devices, and food and industrial tests! Your new company My client has over 20 years experience in developing, manufacturing, and...
As a Quality Lead for site and network complex projects you will be ensuring compliance is considered through all project phases, generate Quality plans, Lead Risk Assessments and Change controls. Cl...
This role is for a high-growth, digital health medical device start-up company who are looking for a Quality Manager to join their expanding team. They are currently working on an in-vitro diagnostic ...
New consumer product in medical device field, working on regulatory submissions & QA activities for compliance Your new company My client is a young business specialising in medical devices and aimi...
You will oversee international trials, oversee CROs and interface with healthcare professionals, clinical investigators, regulatory agencies and internal stakeholders. Client Details My client aim t...
Diagnostics IVD new product launches Clinical Trial Manager wking towards GCP developing medical affairs strategiesWouldnt it be great to look back in five years time and think: "wow. I helped make that happen" This small but growing medical device manufacturer in Cambridge need a Quality Manager, and t...
Quality Manager QA ManagerCK group are recruiting for a Graduate Scientist to join a leading and well established medical diagnostic company, with an international reputation comprising two flagship business divisions that spe...
CK Clinical is recruiting for an Associate Director, Regulatory Affairs to join Boyd Consultants. The role will specialise within medical devices and companion diagnostics and will be part-time (3 day...
Calling all Quality and Regulatory Compliance Specialists!! Are you an experienced Compliance Specialist with experience of working in a medical devices industry Do you have strong experience in creat...
STATISTICIAN / SENIOR STATISTICIAN - CRO/PHARMA - UK HOME BASED Location: Home based, UK. Type: Full time, Permanent. Salary guideline: 45-68k Purpose: Seeking to appoint a Statistician (graduate...
Biostatistics Pharmaceutical Statistics CRO StatisticiansQA / QMS Analyst. In this role you will be responsible to create and implement the QMS at ISO13485 standard. Client Details You will not find public information about the Client (just yet!) as it`s ...
QA / QMS AnalystAn excellent opportunity for a Technical/Medical Writer has arisen with a UK based Diagnostic and Pharmaceutical organisation. This is a chance for a Medical Writer with a strong clinical and regulato...
Industry: Medical Devices Salary: £25,000 - £30,000 Location: Wokingham This is a great opportunity for a Regulatory Affairs Officer to join an exciting start-up company based in Wokingham....
Regulatory Affairs Project Manager Would you like to be part of an organisation which is committed to improving patient lives worldwide through education, collaboration and innovation Do you want to...
IVD BIVDAAre you a Quality Assurance and Regulatory Manager looking for a new opportunity Are you a qualified auditor and have experience of ISO 9001 and ISO 13485 Are you familiar with IVDD and IVDR If so, pl...
CK Group are recruiting for a Technical Assistant to join a leading diagnostics company at their site in Gateshead. This role is being offered on an initial 12-month contract. The Company: Our clien...
Technical Co-ordinator Salary: Negotiable DOE + 26 days holiday + Bank Holidays + Pension Scheme Location: Gateshead with travel to Sunderland site The Requirements: To co-ordinate all ...
As the Quality Assurance and Regulatory Manager you will report directly into the Head of Operations. The primary focus of the role will be to lead and manage all aspects of the QA strategy and regula...
Job title: Senior Scientist Reports to: Validation Team Leader Location: Manchester Contract Type: Full-time, permanent Salary & Benefits: Competitive Salary, Life Assurance, Pension, Private Medi...
Molecular Biology ValidationProduct Quality Engineer Permanent Manchester SUMMARY Responsible for supporting NCEs, product transfers, complaint investigation, QSIand Corrective and Preventative Actions to ensure the maintenanc...
Role: Senior Regulatory Affairs Consultant - Medical Devices (Home based!) Location: EU / USA Salary: Highly Competitive - Perm / Full Time Russell Taylor Group has a fantastic opportunity for a Se...
Medical Devices RA ConsultancyQuality Assurance Manager Salary: £50,000 - £55,000 per annum plus benefits Permanent Blackwood Do you want to be part of a business that makes a real-world impact Helping to play a role ...
Our client based in Longbenton is looking for a IVDR Stability Scientist to join them in their testing team initially on a temporary basis for a period of 6 months. Job Role
A superb, wide-ranging Staff Quality Auditor career development role with BD, a global leader in Medical Technology. BD is a global medical technology company focused on improving ...
Medical Devices Certified Lead Audit ISO 13485 ISO 14971 multinationalOur client is a rapidly growing medical device company developing, manufacturing and marketing smart connected diagnostics and diagnostic-led care solutions. The company has major operations in the UK...
Medical Devices Regulaty Affairs CE Marking ISO 3485 14971 FDA 21CFR IVD/IVDRBring your meticulous standards to our inspirational team When you embark on a career with NHS Blood and Transplant (NHSBT), you’re entering a unique organisation that doesn’t just save and trans...
: Switzerland - Zug, UK - London - Brentford : Aug 18 2020 GSK Global Regulatory Affairs is seeking an Associate Director that can provide critical strategic and operational regulatory leadership ac...
Site Name: Switzerland - Zug, UK - London - Brentford Posted Date: Jun 18 2020 GSK Global Regulatory Affairs is seeking an Associate Director/Director that can provide critical strategic and operatio...
Our client is a fast growing medical device manufacturer with operations in international locations (global business) with locations in UK, China, India, Singapore and most recently the US. They are ...
Molecular Regulaty Affairs Strategy IVD diagnostic ISO13485 licencing Medical DeviceWe are currently supporting a multi-national and market leading business within the field of in-vitro diagnostics (IVD) to recruit a new Regulatory Affairs Manager to join their technical team. The b...
Company Profile Yourgene Health is an international molecular diagnostics group which develops and commercialises genetic products and services. The group works in partnership with global leaders in D...
We are currently supporting a multi-national and market leading business within the field of in-vitro diagnostics (IVD) to recruit a new Regulatory Affairs Manager to join their technical team. The b...
Role:- Laboratory Scientist (media/Uri) Salary:- Competitive (DOE) Location:- Liverpool Russell-Taylor Group have a great opportunity for a microbiologist with a minimum of 2 years commercial exper...
The Company BBI Solutions has served the global diagnostics industry for over 50 years, as a leading developer and manufacturer of raw materials and finished test platforms for the in-vitro diagnosti...
R&D Microbiologist Diagnostics/Pharmaceutical Liverpool £24,000 per annum A fantastic opportunity has arisen for 2 x R&D Microbiologists to join a diagnostics company, who specialise in deliveri...
microbiology; research microbiology; project managementCompany Profile Yourgene Health is an international molecular diagnostics group which develops and commercialises genetic products and services. The group works in partnership with global leaders in ...
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