• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
  • Skip to secondary sidebar

OINDPnews


Proveris Scientific
  • Home
  • News
    • Business
    • Features
    • Medical
    • Regulatory
    • Products and Services
    • People
  • Events
  • Suppliers
    • Supplier listing and advertising options
    • Capsules and blisters
    • Consultants
    • Contract research
    • Contract manufacturing
    • Devices
    • Education
    • Excipients
      • Clinical Technology
    • Filling equipment
    • Instruments
    • Particle manufacturing
    • Software and modeling
  • Jobs
  • Resources
    • Webinars
    • White papers
  • LGWP Propellants
    • HFA 152a
    • HFO-1234ze(E)
    • LGWP Regulation
  • Contact

Inhalation Device Development Engineers

Novartis; Basel, Switzerland

Engineer I and Fellow/Engineer II

Engineer I Job ID number 85034BR
Design, plan, perform, interpret and report results of studies related to development and related processes and procedures of medical devices including the lead and management of all project/local network activities, support/coach of team members, participation in sub-teams and contribution to overall TRD strategies and goals. -Design, plan, perform and contribute to project related to scientific/technical engineering activities and design, plan and perform scientific experiments – Develop efficient and robust devices and processes for the manufacture and/or analysis of Medical Devices/Combination Products (e.g. tolerance analysis, risk analysis) – Coordinate with team members assigned to multiple or complex device development activities – Ensure appropriate planning of workload and resources internally and externally, controlling costs and timescale of the respective project tasks – Report and present scientific/technical results internally and contribute to publications, presentations and patents – Support DRA to prepare select Medical Device/Combination Product pre- registration documents and provides input to answer health authority questions – Support all, and leads select, activities related to the development of the assigned device projects – Support the evaluation of external device collaborations

Minimum requirements Minimum: Apprenticeship in mechanical engineering discipline with continuing education (EU) or BS/MS or equivalent Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent). Good knowledge of English (oral and written). Desirable knowledge of site language. 1. Successfully demonstrated several years (minimum of 3 years) of directly related experience as senior scientist or Ph.D. with post- doctoral/industrial experience (minimum of 1 year) or equivalent. 2. Successfully demonstrated expertise in a specific area. 3. Excellent knowledge of laboratory and/or technical tools. 4. Proficient in utilization of special tools/equipment, lab automation tools and specialized facilities 5. Thorough understanding of development processes in a specific function. 6. Good knowledge of software and computer tools. 7. Profound literature search skills. 8. Ability to work in and/or lead teams. 9. Strong leadership skills. 10. Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies. 11. Very good communication skills. Good presentation skills and scientific/technical writing skills. Advanced coaching skills. 12. May require up to 15% travel

Fellow/Engineer II job ID number 85035BR
Lead and manage all project/network activities and apply scientific/technical expertise to address complex R&D issues for the preparation and timely delivery of drug products (incl. medical devices and packaging aspects), processes and procedures; coach team members, participate in teams and contribute to overall TRD strategies and goals. – plan, perform and contribute to projects related to more complex scientific/technical engineering activities and design, plan and perform scientific experiments. – Develop efficient and robust devices and processes for the manufacture and/or analysis of Medical Devices/Combination Products (e.g. tolerance analysis, risk analysis). – Coordinate with team members assigned to multiple or complex device development activities. – Ensure appropriate planning of workload and resources internally and externally, controlling costs and timescale of the respective project tasks. – Report and present scientific/technical results internally and contribute to publications, presentations and patents. – Support DRA to prepare multiple Medical Device/Combination Product pre-registration documents and provides input to answer health authority questions. – Support all, and leads multiple, activities related to the development of the assigned device / packaging projects. – Drive the evaluation of external device/packaging collaborations.

Minimum requirements Minimum: MS or equivalent Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent). Good knowledge of English (oral and written). Desirable knowledge of site language. 1. Successfully demonstrated several years (minimum of 3 years) of directly related experience as principal scientist or equivalent. 2. Recognized expertise in a specific area. 3. Proven track record in utilization of special tools/equipment, lab automation tools and specialized facilities 4. Thorough knowledge of state-of-art instrumentation/equipment for broad field of applications. 5. Thorough understanding of development processes in a specific function. 6. Profound literature search skills. 7. Ability to work in and/or lead interdisciplinary and/or cross- cultural teams. 8. Proven leadership skills. 9. Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies. 10. Strong communication skills. Strong presentation skills and scientific/technical writing skills. Advanced coaching skills. 11. May require up to 15% travel

To apply online: Engineer I or Fellow/Engineer II

Share

published on October 17, 2011

Primary Sidebar

Sign up for our free weekly newsletter

Upcoming Events
Sponsored by Intertek

Want information about upcoming OINDP-related events delivered directly to your inbox? click here

  • June 17-June 18: Rescon Europe 2025, Paris, France
  • June 19-June 20: Metered Dose Inhaler (MDI) Technology Training Course, online
  • June 22-June 25: ISAM Congress 2025, Washington, DC, USA
  • June 25-June 25: SMI.London 2025, London, UK
  • September 18-September 19: IPAC-RS Nasal Innovation Forum, West Trenton, NJ, USA
  • See all upcoming events

    Secondary Sidebar

    Suppliers

    Capsules and blisters
    Consultants
    Contract research
    Contract manufacturing
    Devices
    Education
    Excipients
    Filling equipment
    Instruments
    Particle manufacturing
    Software and modeling
    Aptar Pharma banner
    © 2025 OINDPnews