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Medical Device jobs

Found 21 jobs
    • United States of America
    • £86000 - £98000 per annum
    • Posted 12 days ago

    In your role you will: Assume technical responsibility in development projects in the field of Class II and III devices Promote the new and further development of mechanical designs for these systems Bring your high creative potential to identify future-oriented innovations Analyse product requir...

    • Belgium
    • €71 - €75 per hour
    • Posted 12 days ago

    MSI Pharma are working with a leading Biopharma in Belgium to help source a Global Quality Lead on a 6 month contract. As part of the Global Quality Assurance organisation, this position provides leadership and QA expertise in driving strategic and operational Quality Assurance activities. - Audi...

    • Switzerland
    • £90 - £100 per hour
    • Posted 12 days ago

    MSI Pharma are working with one of the top pharma companies in the world to hire a Quality Engineer for a 12 month contract in Switzerland. Scope of Work to include the following: Become a working member of the technical file remediation efforts to ensure externally manufactured products meet EU ...

    • United States of America
    • US$81 - US$86 per hour
    • Posted 12 days ago

    MSI Pharma are working with a leading Biopharma to help source a Global Quality Lead on a 6 month contract. As part of the Global Quality Assurance organisation, this position provides leadership and QA expertise in driving strategic and operational Quality Assurance activities. - Auditing experi...

    • United States of America
    • US$120 - US$135 per hour
    • Posted 12 days ago

    MSI Pharma are working with one of the top pharma companies in the world to hire a Quality Engineer for a 12 month contract in Switzerland. Scope of Work to include the following: Become a working member of the technical file remediation efforts to ensure externally manufactured products meet EU ...

    • United States of America
    • US$95 - US$115 per hour
    • Posted 12 days ago

    Well respected client requires a dynamic consultant to join the MDR project team. You will be responsible for all MDR related Regulatory tasks for their products. The required activities include showing an Authorised Representative on all our product labelling, a national product registration and...

    • United States of America
    • US$100 - US$135 per hour
    • Posted 12 days ago

    Well respected client requires a dynamic consultant to join the team The regulations in certain countries and regions require the registrations of new products, perform renewals for the life cycle management and to do change submissions according to the national regulations. Duties New product re...

    • Germany
    • €65000 - €75000 per annum
    • Posted 12 days ago

    Your role: Lead and coordinate development projects in line with internal processes Develop new products in cooperation with brand management, sales and customers Translate user needs and input from markets into technical specifications Ensure communication with stakeholders Establish documents a...

    • Germany
    • €70000 - €85000 per annum
    • Posted 12 days ago

    Your Role: Identifying relevant market insights through interaction with professionals, end users, sales organization, R&D etc Developing, maintaining, and growing relationships with key customers and KOLs Contributes to developing USPs Translating market needs into product features to be then de...

    • Germany
    • £65000 - £75000 per annum
    • Posted 12 days ago

    Your Role: Designing, developing, and launching electronic medical devices Work in close collaboration with Project manager, System engineering and other groups to build the projects requirements Detail Electronic project planning and associated tasks Creating electronic schematic, specifying the...

    • Germany
    • €70000 - €80000 per annum
    • Posted 12 days ago

    Your tasks: As a project manager, assume overall responsibility for innovative product development projects in the field of active implantable devices from the idea to market readiness Lead interdisciplinary, sometimes cross-location and international project teams professionally and collaborate ...

    • Germany
    • €75000 - €85000 per annum
    • Posted 12 days ago

    In your role you will: Assume technical responsibility in development projects in the field of Class II and III devices Promote the new and further development of mechanical designs for these systems Bring your high creative potential to identify future-oriented innovations Analyse product requir...

    • United States of America
    • £86000 - £98000 per annum
    • Posted 12 days ago

    In your role you will: Assume technical responsibility in development projects in the field of Class II and III devices Promote the new and further development of mechanical designs for these systems Bring your high creative potential to identify future-oriented innovations Analyse product requir...

    • England
    • Negotiable
    • Posted 12 days ago

    MSI Pharma are acting as a recruitment partner for a leading and fast growing Notified Body for the Medical Device Industry. Therefore we are constantly looking for medical auditors or technical file reviewers. Dealing with cutting-edge medical innovations, the notified body provides their client...

    • England
    • Negotiable
    • Posted 12 days ago

    Responsibilities Establish and implement the companies Quality Management System (QMS) Oversee all quality-related activities at the company Ensure continuous improvement of the QMS along with GMP and GLP compliance Ensure products are developed and manufactured in accordance with applicable indu...

    • Switzerland
    • Negotiable
    • Posted 12 days ago

    MSI Pharma are partnered with an award-winning medical technology company dedicated to the development, manufacturing and commercialisation of medical devices. For their headquarters in Switzerland we are looking for a Quality Lead Engineer. Your mission Ensure and maintain an adequate, suitable ...

    • Germany
    • Negotiable
    • Posted 12 days ago

    The role Independent implementation of audits according to EN ISO 13485, ISO 9001, MDD, MDR and MDSAP Careful evaluation of the technical documentation of any of the following: orthopaedic, active devices, active implantable, vascular, IVD Independent assurance of the transparent and reliable pro...

    • United States of America
    • Negotiable
    • Posted 12 days ago

    About the job Our client are seeking a Lead Auditor to support their Medical Device division. Your tasks will include: Perform regulatory audits of clients per European Medical Device Directives (IVDD, MDD, AIMD) and new Regulations (IVDR, MDR), Medical Device Single Audit Program (MDSAP), and In...

    • United States of America
    • US$100 - US$135 per hour
    • Posted 28 days ago

    Well respected client requires a dynamic consultant to join the team The regulations in certain countries and regions require the registrations of new products, perform renewals for the life cycle management and to do change submissions according to the national regulations. Duties New product re...

    • United States of America
    • US$95 - US$115 per hour
    • Posted 28 days ago

    Well respected client requires a dynamic consultant to join the MDR project team. You will be responsible for all MDR related Regulatory tasks for their products. The required activities include showing an Authorised Representative on all our product labelling, a national product registration and...