Quality jobs

Found 30 jobs
    • Region Hannover
    • Negotiable
    • Posted 1 day ago

    Job Summary: We are seeking a dedicated and detail-oriented Complaint Specialist to join our team. The ideal candidate will have experience as a dialysis technician or nurse and will be responsible for managing and resolving customer complaints related to our medical devices. This role is critica...

    • Region Hannover
    • Negotiable
    • Posted 1 day ago

    Job Summary: We are seeking a dedicated and detail-oriented Complaint Specialist to join our team. The ideal candidate will have experience as a dialysis technician or nurse and will be responsible for managing and resolving customer complaints related to our medical devices. This role is critica...

    • Region Hannover
    • Negotiable
    • Posted 1 day ago

    Job Summary: We are seeking a dedicated and detail-oriented Complaint Specialist to join our team. The ideal candidate will have experience as a dialysis technician or nurse and will be responsible for managing and resolving customer complaints related to our medical devices. This role is critica...

    • Deutschlandsberg
    • Negotiable
    • Posted 3 days ago

    I am currently working with a global leader in medical devices, dedicated to advancing healthcare through innovations in cardiology, orthopedics, surgical robotics, and diagnostics. They are currently looking for a GPO Tender Manager to join their expert team. Key Role Highlights: As a GPO Tender...

    • Germany
    • Up to โ‚ฌ24000 per annum
    • Posted 3 days ago

    I am working with a global leader in medical devices, dedicated to advancing healthcare through innovations in cardiology, orthopedics, surgical robotics, and diagnostics. They are currently looking for a GPO Tender Manager to join their expert team. Key Role Highlights: As a GPO Tender Manager, ...

    • San Diego
    • US$120000 - US$140000 per year
    • Posted 4 days ago

    About Are you ready to make a real impact in the field of non-opioid pain management? This company is a leading provider of non-opioid pain management and regenerative health solutions. Our commitment to advancing patient care drives us to address unmet medical needs and improve clinical results....

    • Negotiable
    • Posted 4 days ago

    ๐——๐—ฒ๐—น๐˜๐—ฎ๐—ฉ ๐—•๐—ฎ๐˜๐—ฐ๐—ต ๐—˜๐—ป๐—ด๐—ถ๐—ป๐—ฒ๐—ฒ๐—ฟ - 12-๐— ๐—ผ๐—ป๐˜๐—ต ๐—–๐—ผ๐—ป๐˜๐—ฟ๐—ฎ๐—ฐ๐˜ | ๐——๐˜‚๐—ฏ๐—น๐—ถ๐—ป | ๐—™๐—Ÿ๐—ฆ ๐—ฆ๐—ต๐—ถ๐—ณ๐˜ Currently seeking an experienced ๐——๐—ฒ๐—น๐˜๐—ฎ๐—ฉ ๐—•๐—ฎ๐˜๐—ฐ๐—ต ๐—˜๐—ป๐—ด๐—ถ๐—ป๐—ฒ๐—ฒ๐—ฟ for a 12-๐—บ๐—ผ๐—ป๐˜๐—ต ๐—ฐ๐—ผ๐—ป๐˜๐—ฟ๐—ฎ๐—ฐ๐˜ at a leading ๐—ฝ๐—ต๐—ฎ๐—ฟ๐—บ๐—ฎ site in Dublin. This role is key to supporting critical manufacturing operations in a fast-paced, high-tech environment. ๐Ÿ”น12-๐—บ๐—ผ๐—ป๐˜๐—ต ๐—ฐ๐—ผ๐—ป๐˜...

    • Ohio
    • Negotiable
    • Posted 4 days ago

    Location: Midwest, USA (with Travel Requirements) EPM is working with an exceptional medical device company in the Midwest that is seeking experienced Senior Quality Engineers to join their team. This company specializes in ophthalmology, cardiovascular, and dental medical devices and is dedicate...

    • Brisbane
    • US$220000 - US$250000 per year + 401k, Dental, Medical, Vision
    • Posted 10 days ago

    Position: The Senior Director, Quality Systems will serve as a subject matter expert and will assist in the implementation and maintenance of GxP compliant procedures and operations by managing the GxP systems including electronic document management system and learning management system. This ha...

    • Stuttgart
    • Negotiable
    • Posted 11 days ago

    Key Responsibilities: Perform technical assessments of active medical devices, ensuring compliance with MDR 2017/745 and international regulatory standards. Conduct conformity assessments, design dossier reviews, and clinical evaluations for medical devices. Lead and participate in regulatory aud...

    • Stuttgart
    • Negotiable
    • Posted 11 days ago

    Key Responsibilities: Conduct technical file reviews, risk assessments, and clinical evaluations of non-active medical devices. Perform conformity assessments and certification evaluations under MDR 2017/745 and related standards. Lead and participate in regulatory audits (ISO 13485, MDSAP, MDR) ...

    • Netherlands
    • Negotiable
    • Posted 11 days ago

    We are currently supporting a Quality Assurance Officer position for a client based in The Netherlands. Quality Assurance Officer Our client is an innovator in Global Health and is currently looking for a Quality Assurance Officer to join the team! Main Responsibilities of a Quality Assurance Off...

    • Weybridge
    • Negotiable
    • Posted 15 days ago

    We are currently supporting a Qualified Person and Responsible Person position for a client based in the London. Qualified Person and Responsible Person Our client is an innovator in the consumer health space and is currently looking for a Qualified Person and Responsible Person to join the team!...

    • Weybridge
    • Negotiable
    • Posted 15 days ago

    We are currently supporting a Qualified Person and Responsible Person position for a client based in the London. Qualified Person and Responsible Person Our client is an innovator in the consumer health space and is currently looking for a Qualified Person and Responsible Person to join the team!...

    • Norway
    • Negotiable
    • Posted 15 days ago

    Job Description: Medical Device Assessor & Lead Auditor - Non-Active Devices Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct technical file reviews, risk assessments, and clinical...

    • Germany
    • Negotiable
    • Posted 15 days ago

    Job Description: Integrated Clinician - Medical Devices (Active & Non-Active) Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct clinical evaluations and assessments of active and no...

    • Germany
    • Negotiable
    • Posted 16 days ago

    We are currently working with a reputable Solutions Provider in the pharmaceutical and medical device industry looking for an experienced Quality Management & Compliance professional to join the team in Germany. This is an exciting opportunity to work within a growing team, partnering with leadin...

    • City of London
    • Negotiable
    • Posted 18 days ago

    We are currently supporting a Process Engineer position for a client based in the London. Process Engineer Our client is an innovator in the Medical Device space and is currently looking for a Process Engineer to join the team! Main Responsibilities of a Process Engineer Facilitating the design, ...

    • Stuttgart
    • Negotiable
    • Posted 19 days ago

    Head of Non-Active Medical Devices - Leading Notified Body We are representing a leading Notified Body seeking an experienced Head of Non-Active Medical Devices to join their team. This is a pivotal leadership role within a globally recognized organization, providing regulatory expertise, strateg...

    • Hamburg
    • Negotiable
    • Posted 23 days ago

    Your Responsibilities: Ensure compliance with the risk management process according to ISO 14971 for new developments and existing therapy products. Coordinate, create, and maintain risk management files for new developments, the existing portfolio, and change management in therapy products. Anal...

    • Bethesda
    • Negotiable
    • Posted 24 days ago

    About the Role A leading Notified Body is seeking an experienced Medical Device Auditor with expertise in IEC 60601-1 (Electrical Safety) and Medical Device Software to join its growing team. This role is crucial in ensuring that medical electrical equipment and software-driven devices comply wit...

    • Bethesda
    • Negotiable
    • Posted 24 days ago

    A leading Notified Body is seeking experienced Medical Device and In Vitro Diagnostic (IVD) Product Reviewers / Auditors to join its growing certification and regulatory compliance team. This role is crucial in ensuring that medical devices and IVD products meet the highest safety, quality, and r...

    • London
    • Negotiable
    • Posted 24 days ago

    A leading provider of certification, audit, and assurance services is seeking a highly skilled professional to join its Assurance Services team as a Lead Auditor. With over 70 years of experience in the UK, the organization ensures that products and systems are safe, reliable, and compliant by of...

    • Munich
    • Negotiable
    • Posted 25 days ago

    We are looking for a highly skilled individual to assist the quality management and touchpoints with regulatory bodies across various business units or subsidiary companies with a specific focus on Europe and other regions. Responsibilities Establish and maintain Quality System requirements effec...

    • Vienna
    • Negotiable
    • Posted 25 days ago

    Job Title: Freelance eQMS Specialist Duration: 6 Months Industry: Pharmaceutical We are looking for a Project Quality Management Specialist to support the modernisation and update of our Electronic Quality Management System (eQMS) on a freelance basis. This is a contract position for six months, ...

    • North Carolina
    • Negotiable
    • Posted 25 days ago

    . The Contractor Quality Associate, Biologics plays a critical role in data management of commercial biologics executed by contract laboratories. The position requires familiarity with data review, data management in Excel or Minitab, and understanding of LIMS systems. Some understanding or famil...

    • Frauenfeld
    • Negotiable
    • Posted 25 days ago

    Job Description: This Exclusive mandate seeks a highly experienced and motivated Global Head of Quality and Regulatory with direct leadership expertise and hands on mentality to join a dynamic client in the medical device field. This leadership role is critical in ensuring our products meet the h...

    • United States of America
    • Negotiable
    • Posted about 1 month ago

    Overview: EPM is hiring on behalf of a leading medical device manufacturer recognized for its innovation and excellence in producing active medical devices and software solutions. This hybrid position offers a unique opportunity to play a pivotal role in ensuring the quality and compliance of cut...

    • Italy
    • Negotiable
    • Posted about 2 months ago

    ABOUT US We are a European organization recognized as an official Notified Body under Regulation (EU) 2017/745, specializing in verifying the conformity of medical devices with the stringent requirements of the MDR 2017/745 regulation. Our work ensures that medical devices meet the necessary stan...

    • United States of America
    • Negotiable
    • Posted about 2 months ago

    Senior Specialist, Quality Systems We are seeking a highly skilled Senior Quality Systems Specialist to join a growing Contract Development and Manufacturing Organization (CDMO). In this role, you will be responsible for managing and enhancing quality management systems (QMS) to ensure compliance...

Get new jobs for this search by email