Iso 13485 Jobs in Kathmandu

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...

Bachelor’s degree in Life Sciences, Engineering, Technical Writing, or a related field; advanced degree preferred Minimum of 6 years of experience in regulatory writing, preferably within the medical device industry Strong understanding of regulatory requirements and guideli 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...

Role: Senior Quality Systems Specialist Location: Illinois Duration: Permanent Salary: $110000$115000K Job Description: We are establishing a new department and seeking an individual to join our team as a Senior Quality Systems Specialist in a manufacturing company specializing i 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...

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...

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...

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...

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...

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...

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...

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...

Role name: Project Manager Role Description: Project Managements Quality Management Systems PMP FDA Power Point Presentation Strong communication skills ISO 13485 Medical Device Regulatory Standards Quality Compliance CAPA / NC Competencies: EIS : Medical Device & Re More...

Role: Sr System Engineer Location: Pittsburg PA Onsite Job Description: 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 Ma More...

Quality Management ISO 13485 Medical Device Regulatory Standards Quality Compliance CAPA / NC Windchill PLM system Quality Engineer A minimum with 5 years of related experience Quality Management in Medical Device Industry Knowledge of Medical procedure and corresponding Medical Equi 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...