Iso 13485 Jobs in Ljubljana

Tasksmanage quality operations within the shopwill be a handson rolewill measure partswill oversee audits for their AS9001 and ISO 13485 certificationswill have 2 direct reports that are Quality TechniciansRequirements3 years experience in manufacturingISO 9001 or ISO 13485 experience More...

Taskstest and inspect parts in a stateoftheart medical machining operationuse mics calipers and gaugesuphold ISO 13485 standards and FDA standardshandle documentation and setup quality processesvery handson roleRequirements35 years quality experiencemics calipers gaugesmust have ISO 1 More...

Job Title: Manufacturing Engineer location: Westbrook ME Duration: 02 Months BASIC QUALIFICATIONS EDUCATION: Bachelors degree (BS) in engineering or equivalent combination of education and experience. Minimum three years engineering experience in a manufacturing environmen More...

We Vivalyx are a medical technology startup from Aachen dedicated to saving people suffering from organ failure. Our goal is to significantly increase the vitality and number of donor organs. The company is currently in the preparation phase for certification and the associated studie More...

Mit unserem innovativen Unternehmen in der Medizintechnik konzipieren und fertigen wir Atemtherapie und Heimbeatmungsgerte fr den globalen Markt. Unser Fokus liegt darauf sowohl Patienten als auch medizinischem Personal ein effizientes und benutzerfreundliches Gert zur Verfgung zu ste More...

Role name: Engineer Role Description: Quality Management Systems FDA Presentation Strong communication skills ISO 13485 Medical Device Regulatory Standards Quality Compliance CAPA / NC Competencies: EIS : Medical Device & Regulations Experience (Years): 68 Essential Skills: A minimum More...

Senior Supplier Quality Engineer Irvine CA Onsite Hire Fulltime Hire Job Skills and Responsibilities: Working knowledge of regulatory compliance requirements i.e.Quality System Regulations (QSRs) Medical Device Directive (MDD) ISO 9001 ISO 13485 ISO 14971. Provides overall qua More...

Our client a growing Cell Therapy company is looking for a Manufacturing Planning Supervisor. The job responsibilities are as follows: 1. Production and Warehouse Oversight: Manage and oversee both production and warehouse activities to ensure seamless operations. Manufactu More...

Role : QA Engineer Location: Irvine CA (Onsite) Duration: Contract A minimum of 7 years of experience in Quality Engineering or Quality Assurance including data analysis risk assessment and risk mitigation is required. Working experience in good manufacturing practice regulated e More...

Job Title : Quality Lead Warren NJ (100% On site) 23 months Contract Company: RCM Life Sciences Rate is $35/hr on C2C If your candidate has no lead experience still I will try as rate is very low. Quality Lead Do you thrive on meticulous details and ensuring quality stan More...

Medical device manufacturer in the greater Knoxville TN area has an immediate opening for a Quality Manager. This is a smaller company that develops and manufacturers complex equipment for use in hospital settings. This Quality Manager will be responsible for handling 3rd party audits More...

Job Description: Position Summary:The Technical Writer II is responsible for supporting the Quality Assurance and Regulatory Affairs teams by creating revising and maintaining documentation related to IVDR submissions. This role works crossfunctionally with Manufacturing Operations an More...

Project Manager Medical Device Experience Irvine CA or Danvers MA Onsite Hire Fulltime Hire Job Skills and Responsibilities: Project Management Professional (PMP) certification is required Must possess knowledge of theoretical and practical fundamentals and experimental en More...

Job Description: Position Summary:The Technical Writer II is responsible for supporting the Quality Assurance and Regulatory Affairs teams by creating revising and maintaining documentation related to IVDR submissions. This role works crossfunctionally with Manufacturing Operations an More...

Vi leder efter en udadvendt QA Manager til vores voksende team i Herlev. Er du klar til at st i spidsen for vores quality assurance og trives du med at arbejde bredt tvrfagligt og hele tiden lre nyt s har vi en spndende mulighed hos Prevas. Som QA Manager vil din base vre at sikre kv More...

Job Title Quality Supplier Engineer Location Irvine CA Job Description: Quality Management ISO 13485 Medical Device Regulatory Standards Quality Compliance CAPA / NC Windchill PLM system. EIS : Medical Device & Regulations 46 Quality Engineer A minimum with 5 years of r More...

The Quality Assurance Manager will be responsible for managing the quality management system and ensuring regulatory compliance for the companys products processes and services.Oversee the companys adherence to domestic and international regulatory standards including FDA regulations More...

We are looking for a Quality Assurance Engineer for our growing partner an internationally listed company dealing with development production and distribution of medical devices. As a member of the quality team you will participate in projects in cooperation with other departments an More...

For further inquiries regarding the following opportunity please contact one of our Talent Specialists Sivanesan at Divya at Rashi at Title: Systems Engineer 2 (EARS)REMOTE Location: Remote (Candidate needs to be West Coast) Duration: 1.5 Years Job Summary: We are seeking a high More...

Essential Skills: A minimum of Technical/Engineering Degree with 8 years of related experience Medical Device Supplier Quality domain. Working knowledge of regulatory compliance requirements (i.e. Quality System Regulations (QSRs) Medical Device Directive (MDD) ISO 9001 ISO 13485 ISO More...