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Job Title: Quality Assurance and Regulatory Affairs Specialist Location: Cambridge(Hybrid, 2-3 days per week onsite) About: A distinguished medical device company based in Cambridg...
* Proven experience of EU and US medical devices regulations * Experience of ISO 13485 QMS. * Compilation of Technical Files/Documentation to MDD 93/42/EEC or MDR Our client is seeking a Projects Man...
Our 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 DeviceRemoteCERProcess and Servicing Engineer Coventry £30,000 - £35,000 Based in Coventry, West Midlands. Partial remote work flexibility considered a...
Our client operates in the Medical Devices sector of business and the successful candidate will need to work within this regulatory framework in the Technical Quality department and be responsible for...
Regulatory 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 13485MDDUKCAMDSAPIVDRThe Quality Manager will be developing and managing the companys Quality Management System (QMS) in compliance with the requirements of ISO 13485 and MDSAP, along with the creation and measurement of ...
Adecco is looking to hire a Regulatory Manager to support a Medical Device business on a permanent basis. Working with a small team of Regulatory Specialists you will oversee the compliance of new an...
RegulatoryMDRregulatory affairssubmissiontechnical fileRegulatory Affairs Officer (Medical Device) Remote, £32-40k Our client, a rapidly growing Medical Equipment Manufacturing organisation are looking for a RA Officer to join their...
Regulatory Affairs Officer (Medical Device) Remote, £32-40k Our client, a rapidly growing Medical Equipment Manufacturing organisation are looking for a RA Officer to join their...
Responsible to plan, manage and control the manufacturing processes, monitor performance versus targets ensuring that goods are produced efficiently and that the correct amount is produced to the righ...
Our client operates in the Medical Devices sector of business and the successful candidate will need to work within this regulatory framework in the technical department and be responsible for the Qua...
CAPAData CollectionProcess ControlResponsible for Quality Management System (QMS) and for ensuring that the QMS meets ISO 13485, MDSAP (Medical Device Single Audit Programme) and other international standards and regulations required ...
GMP Production Manufacturing Technician Opportunity - Hertfordshire Opportunity: An exciting opportunity has been created due to company growth. My client a global...
Drug DevelopmentGMPPharmaceutical ManufacturingProduction ManagementClean RoomsOur client is part of a group of global medical device companies. The brand specialise in sterile single-use surgical instruments, priding themselves on developing new and innovative products that are...
Medical DevicesRegulatory AffairsRisk ManagementMDRTechnical FilesISO 13485MDDUS FDAOur client is a fast growing digital health company developing an app-based platform that uses artificial intelligence (AI) to predict an individuals risk of developing complications from their diabet...
BiotechnologyPharmaceuticalRegulatory AffairsQualityMedical DeviceDigital HealthOur client is part of a group of global medical device companies. The brand specialise in sterile single-use surgical instruments, priding themselves on developing new and innovative products that are...
FDAMedical DevicesRegulatory AffairsRisk ManagementMDRMHRAISO 13485MDDMarket ApprovalWe 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...
Our client is a fast growing digital health company developing a app-based platform that uses artificial intelligence to predict an individuals risk of developing complications from their diabetes inc...
Medical DevicesRegulatory AffairsRisk ManagementMDRISO 27001ISO 13485IEC 62304MDD510KCE MarkDigital HealthMarket approvalA Quality Systems Specialist is required by a medical device manufacturer to work on projects ensuring quality compliance and ensure teams are supported. This role is based in Wokingham and will be ho...
quality| specialist| medical| FDA| ISO13485| data| SAP| QMS| SharePoint| QMS| MDSAP| medicaldeviceAn opportunity has come up for a Quality Manager to join an established optical / medical device company in the Nottinghamshire area. In this exciting role we will look to you to cre...
JOB- QA / RA Manager – Medical Devices LOCATION- South East TERM- Permanent SALARY- £45,000 - £75,000 per annum (dependent on experience) We are looking for a Quality Assurance / Regu...
Kimal is an innovative and trusted manufacturer and supplier of specialised procedure packs and vascular access devices to hospitals across the world. We are proud of our achievements and we strive to...
A highly exciting role to join one of the regions leading and fastest growing pharmaceutical businesses in a newly created post. The position will work as part of the compliance, QA and regulator aff...
Kimal is an innovative and trusted manufacturer and supplier of specialised procedure packs and vascular access devices to hospitals across the world. We are proud of our achievements and we strive to...
Do you have experience in quality management and are looking for your next role We are looking for a quality manager to join our production team in our retail fulfilment hub. In this exciting role we ...
Our expanding manufacturing client are recruiting for an experienced Quality Engineer to join their growing operation. In this key role, you will assist the head of Quality to ensure that product and...
A leading medical device manufacturer has an exciting opportunity for a Microbiology Manager to join its team. You will be responsible for the overall management of the Microbiology Lab with 5 direct ...
Medical Device - ISO 13485 - Aseptic - SterileAre you an experienced regulatory professional within medical devices We are seeking an experienced regulatory manager to join a Times Top 100 employer, implantable medical devices company based in Le...
Biology Chemistry Medical Devices Staff Development Technical FilesCK Group are recruiting for a Quality Specialist/Engineer to join a medical technology company at their sites based across central Scotland on a permanent basis. The Company: Our client is a medica...
CK Science are recruiting for a Quality Officer to join the Quality Support function of a rapidly growing research and development company in the diagnostics sector. The Shift QA Officer will be worki...
CK Technical are recruiting for a Quality Engineer to join a medical technology company at their sites based across central Scotland on a permanent basis. The Company: Our client is a medical techn...
CK Technical are recruiting for Senior Quality Engineer to join a medical device and diagnostics company at their sites based across central Scotland on a permanent basis. The Company: Our client i...
Description Regulatory AffairsSpecialist Would you like to be part of an organisation which is committed to improving patient lives worldwide through education, collaboration and innovation Do you ...
live sciencesRegulatory 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 BIVDACompany Description SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and i...
JOB- Medical Devices Quality Manager LOCATION- South East / Remote TERM- Permanent SALARY- £40,000 - £60,000 per annum (dependent on experience) We are looking for a Quality Manager on ...
Here at the Binding Site, we have all experienced the impact that the pandemic has had both on a personal and professional level, and as an organisation we are committed to fight against Covid-19. Wor...
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 multinationalSummary To ensure the appropriate licensing, marketing and legal compliance of the Medical and Scientific portfolio. This role represents a key position within the RAQA organisation since they need t...
Exciting opportunity to join a world leading medical device business who are constantly updating, developing and releasing new life changing technology. Client Details My Client is a world leading m...
Medical Device Lead Auditor Location: UK, Field based - National(Company Car provided) Permanent, 37.5 hours per week Job Description We have an excellent new opportunity for a Medical D...
Real Staffing, part of the SThree group, are looking for a Quality Engineer to join one of their clients during a period of rapid and sustained growth. If you can demonstrate experience in being respo...
MEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR Locations: Anywhere Home Based UK. Salary: Negotiable Eur. Work from Home/Remote: Yes. Travel: Yes (0% during Covid19). Bonus: ...
Auditing Medical Devices Product Development Regulaty Affairs CE markingMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Development Regulaty Affairs CE markingMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Development Regulaty Affairs CE markingMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Design Product Development Regulaty AffairsMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Design Product Development Regulaty AffairsMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Design Product Development Regulaty AffairsMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Development Regulaty Affairs CE markingMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Development Regulaty Affairs CE markingMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Development Regulaty Affairs CE markingMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Development Regulaty Affairs CE markingMEDICAL DEVICE PRODUCT EXPERT/PRODUCT SPECIALIST/REGULATORY AUDITOR. Locations: Anywhere Home Based in USA. Salary: Negotiable 80-110k USD. Work from Home/Remote: Yes. Travel: Yes (0% during Covid...
Biomedical Medical Devices Product Development Regulaty Affairs CE markingOtodynamics Ltd, based in Hatfield Hertfordshire has designed and manufactured electronic medical hearing testing instruments for sale to hospitals/private clinical and military facilities around the ...
Assembly Medical Devices Process Improvement Soldering Electronic EngineeringQuality Assurance / Regulatory Affairs Officer Salary Guide: £27,000 - £30,000 Harlow, Essex - Free on-site Parking Established medical instrumentation design and manufacturer are looking...
Regulaty Affairs MDR ISO 13485 ISO13485 MDD 93/42/EEC MDSAPWe currently have an opportunity available for a Quality Manager to join us to take accountability for the implementation, development and continual compliance of the Quality Management System and Env...
Our client is a leading Medical device organisation who is presenlty for a QA Manager to join their expanding team at their site in North East England. As this role will be responsibilities for eleme...
ISO Medical Devices Quality Assurance Quality Management IVDTechnical Support Engineer required for a 6 month contract role with a leading multinational client based in Hull. The role The Role Holder provides support to the AWD Service and Repair organizatio...
Service and Repair Engineer required for a 6 month contract role with a leading multinational client based in Hull. The role The Role Holder provides support to the AWD Service and Repair organizati...
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