Iso 13485 Jobs in Hamburg

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 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...

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...

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...

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...

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...

This is a management position where the employee plans and directs activities with development application and maintenance of quality standards for industrial processes materials and products to ensure continuous steel processing production consistent with established standards custom More...

Hello Trust this email finds you in good cheer!! Im Rupender from SiriInfo. I have an opportunity with me you might be interested please review the Job specifications below and let me know if you may be interested in this opening or may refer someone to me for this. For you referen 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...

Project Manager A minimum of Technical/Engineering Degree with 10 years of related experience Medical Device Product Management domain. Project Management Professional (PMP) certification is required Must possess knowledge of theoretical and practical fundamentals and experimental 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...

Job Description: Essential Functions Operates and/or monitors production equipment and makes necessary adjustments to ensure smooth operations and high quality results if required in work area. Works alone or with other technicians to perform filling labeling and/or packaging of More...

Job Description: Essential Functions Operates and/or monitors production equipment and makes necessary adjustments to ensure smooth operations and high quality results if required in work area. Works alone or with other technicians to perform filling labeling and/or packaging of More...

Job Description Business Analyst ISO Compliance 10 years of Insurance experience preferably in Property & Casualty (P&C) Insurance. Insurance policy and claims system experienced. Must have an experience on US Insurance Compliance like ISO Regulatory Statutory Repo More...

Strong knowledge in Banking Payments Domain. Provides subject matter expertise internally for ISO 20022 training and the preparation of proposals for CBPR and FedNow payment messaging requirements. Provided detailed subject matter expertise to the clients Professional Services t More...