Iso 13485 Jobs in Slovenia

Overview: TekWissen Group is a workforce management provider throughout the India and many other countries in the world. The below job opportunity is to one of Our clients which is a research and innovation driven UL registered and ISO 13485:2016 ISO 9001:2015 and ISO 45001:201 More...

Quality Engineer5 years of work experience in the Medical Device industry in Quality role Understanding on Medical Device Quality and Compliance Knowledge on ISO 13485: 2019 and 21 CR 820 Experience in Complaints Handling Post Market Surveillance Knowledge on Medical D More...

Position Overview: The Quality Manager is responsible for the direction and management of all Quality Department functions. The Quality Manager guides the team through auditing procedures, maintains industry standards, assists with inspection to ensure quality and problems solved as n More...

Overview: TekWissen Group is a workforce management provider throughout the India and many other countries in the world. The below job opportunity is to one of Our clients which is a research and innovation driven UL registered and ISO 13485:2016 ISO 9001:2015 and ISO 45001:201 More...

We are Una a missiondriven company tackling the everincreasing burden of metabolic disease.We are combining the latest medical research data science biosensor technology and humancentered design to enable sustainable behaviour change and improve health outcomes.We have created the fir More...

Job Title: Manufacturing Supervisor Synthesis and Production Microbiology Duration: 12 Month Shift: 7:00 am 3:00 pm PST Work Location: San Diego CA 92127 SUMMARY: The main responsibility for the Synthesis and Production Microbiology Supervisor is to lead and oversee all p More...

As the Director Quality and Regulatory Affairs (m/f/d) you support business units and functions in creation implementation and maintenance of processes and related documented information.TasksAs the Director Quality and Regulatory Affairs (m/w/d) you support business units and functio More...

Job Title: Quality Management System CoordinatorCompany: A leading French company specializing in the design and manufacture of Orthopedic Medical Devices for extremity surgery. With a global presence across 14 subsidiaries and a distribution network spanning five continents the compa More...

The role of the Assembler III for 1st and 2nd shifts is to perform and ensure production assembly tasks are actively completed to meet production schedules while upholding the highest level of Quality. The assembler will assemble products by using a variety of hand and power tools More...

Ensure that the client’s QMS conforms to all ISO 9001, and regulatory/legal requirements. Oversee inspection (examination) of incoming materials, ensuring that they meet requirements. Manage the monitoring, measurement, and review of internal processes, esp More...

Our client is looking for a Sterility Assurance Specialist III for a 6+ months contract role in Alpharetta, GA. To provide technical expertise in the terminal sterilization sciences for medical devices products Skills: Candidate should have some knowledge of microbiology and More...

Company Overview: Our company is a leading provider of highquality engineering and manufacturing services offering solutions to a diverse range of industries such as aerospace defense medical industrial and telecommunications. We strive to deliver innovative reliable products and serv More...

We are status quo breakers game changers and pathway makers!With our health platform myoncare we are transforming the healthcare market and as a leading ecosystem we want to enable excellent healthcare support for all patients in the world.How do we do thatPeople are at the center of More...

We are looking for an Information Security and Compliance Analyst for our Compliance team.Experience:1 to 3 YearsLocation:MohaliJob Responsibilities:Develop implement and maintain compliance programs and initiatives to ensure adherence to security requirements for ISO 27001:2022 SOC 2 More...

We are status quo breakers game changers and pathway makers!With our health platform myoncare we are transforming the healthcare market and as a leading ecosystem we want to enable excellent healthcare support for all patients in the world.How do we do thatPeople are at the center of More...

Drfr r detta jobbet fr digDu vill frbttra livskvalitn fr patienter genom skra medicintekniska produkter.Genom att hitta rtt niv av kvalitet och regulatorisk efterlevnad genom produktutvecklingsprocessen vill du vara en viktig del i att introducera ny teknik och mer effektiv medicintek More...

Ensure that the client’s QMS conforms to all ISO 9001, and regulatory/legal requirements. Oversee inspection (examination) of incoming materials, ensuring that they meet requirements. Manage the monitoring, measurement, and review of internal processes, especially those that More...

Description: Pay rate XX20.50 Daytime hours Job Description Summary This position is responsible for conducting routine inspection and analysis of incoming service material and quality reviews of domestic and international service records by identifying conflicts dependencies and r More...

We are status quo breakers game changers and pathway makers!With our health platform myoncare we are transforming the healthcare market and as a leading ecosystem we want to enable excellent healthcare support for all patients in the world.How do we do thatPeople are at the center of More...

Description: Pay rate $$$ Daytime hours Job Description Summary This position is responsible for conducting routine inspection and analysis of incoming service material and quality reviews of domestic and international service records by identifying conflicts dependencies and risk More...