Iso 13485 Jobs in Slovenia

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...

Position Summary: We are hiring a highly dedicated QA/RA Manager who will manage all quality matters in the company and act as the Management Representative as defined in the ISOCFR Part 820 (FDA cGMP) Regulation (EU) 2017/745 or any other relevant standards and regulations.Job Respo More...

Position Summary: We are hiring a highly dedicated NPI Engineering Manager who will oversee and manage all Project Management and NPI activities on in the company.Job Responsibilities: Taking the necessary action to ensure that the standards related to ISO 13485 GMP product ISO stand More...

Position Summary: We are hiring a highly dedicated NPI Engineering Manager who will oversee and manage all Project Management and NPI activities on in the company.Job Responsibilities: Taking the necessary action to ensure that the standards related to ISO 13485 GMP product ISO stand 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...

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...

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...

Neurosoft Bioelectronics situated in Geneva Switzerland is at the forefront of medical equipment manufacturing specializing in innovative solutions for interfacing with neural tissue. Our mission is to revolutionize the treatment of severe neurological disorders such as epilepsy tinni 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...

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...

Mandatory Skills: Systems Engineering for Electromechanical Medical Devices InCose certification ISO 13485 ISO 14971 IEC 62304 Usability for Medical devices Regulatory for Medical Devices Requirements Management Jira IEC 606011 and any Particular standards. Overall technical leade 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...

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...

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...

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...