ISO 13485 Jobs in UK

We are seeking a highly skilled consultant with experience in medical device and/or combination product Quality and Regulatory processes to join our Healthcare & Life Sciences (HLS) consulting team. This role focuses on advising clients on the regulatory Quality and compliance aspects of medical dev...

1.執行稽核及撰寫稽核報告2.擔任課程講師3.主管交辦事項Qualifications : 1.具英文閱讀書寫能力中等以上2.配合工作性質需自備交通工具3.具講師經驗者尤佳 其他資訊 : SGS價值觀 熱情 Passion誠信 Integrity企業家精神 Entrepreneurship開創性 Innovative Spirit 福利公司制度週休二日優於勞基法工時制度保險制度勞保健保...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsLaboratory Setting OfficeJob DescriptionJob Description Business Job Title: System Verification Engineer I Job Profile Title: Engineer I Systems DesignDirect Report To: Chad OwensGroup/ Division: Protein DiagnosticsCareer Band: 4 Career Track: R...

DescriptionThe Head of Digital Technical Support provides strategic direction and operational oversight for all global software support functions. This role ensures an effective customer experience through efficient incident response escalation leadership proactive monitoring service automation and...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOffice Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)Job DescriptionLocation / Division Specific InformationThis position is based at the Inchinnan U.K. site and supports suppl...

DescriptionSenior Product Quality EngineerJoin a team where your expertise directly improves the quality safety and performance of lifechanging medical technology. As a Senior Product Quality Engineer you will help ensure that devices used in healthcare settings worldwide meet the highest standards...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Job descriptionEnsera Design is a world-class user-centred innovation and product development consultancy specializing in the medical and consumer health sectors with offices in Bristol Colorado and New Jersey. As part of Ensera we collaborate globally with contract manufacturing facilities in Europ...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make...

 Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However the actual time you spend and where you spend it will vary by role or assignment including up to 5 days per week on a client site.This role can be based at either our London Victoria or Melb...

Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However the actual time you spend and where you spend it will vary by role or assignment including up to 5 days per week on a client site.This role can be based at either our London Victoria or Melbo...

Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However the actual time you spend and where you spend it will vary by role or assignment including up to 5 days per week on a client site.This role can be based in our London Victoria or Melbourn off...

Hybrid working - our approach is to be in the office or on client site a minimum of 2 days per week. However the actual time you spend and where you spend it will vary by role or assignment including up to 5 days per week on a client site.This role can be based in our London Victoria or Melbourn off...

DescriptionSenior Manager Regulatory AffairsAt Endomag a Hologic company we are driven by a clear purpose: advancing health through innovative medical technologies that improve and save lives. We are seeking an experienced Senior Manager Regulatory Affairs to lead the Regulatory function at our Camb...

Supplier Quality Engineer (SQE)We are seeking a proactiveSupplier Quality Engineer to ensure materials components and services from our suppliers meet quality regulatory and performance standards. Working cross-functionally with Engineering Quality Consumables and Supply Chain you will play a key ro...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Laboratory Setting Office Some degree of PPE (Personal Protective Eq...

Quality in a globalized supply chain is a matter of operational resilience as much as regulatory mandate. This role serves as a GMP Auditorwithin our Research & Development Quality audit program responsible for executing the global audit plan to ensure the accuracy of scientific data and compliance...

Role Overview - FULL TIME ONSITE IN COVENTRY. APPLICATIONS FROM HCPC UK RESIDENTS ONLY We are seeking an experienced HCPC-registered Laboratory Scientist to play a key role in a growing molecular diagnostics laboratory and support the clinical deployment of a novel endometrial function test. This...

DescriptionJob title: Principal Regulatory Affairs Specialist - EMEADepartment: Regulatory AffairsLocation:Southampton UK / Gorinchem Netherlands or Gothenburg SwedenGLS: P04Working hours: UK 37.5 hours per week Netherlands or Sweden 40 hours per weekA brighter future awaits youWhat to expect:The...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...