About the Role
Support the manufacturing of chemistry based medical devices products by maintaining current processes and transferring new processes from R&D. The scope of work includes process and test method validation, identifying and implementing process and test method improvements, process transfer and scale-up. Work closely with R&D, Quality, and Regulatory in supporting the transfer of new products from R&D, process and test method validation, and process development and improvement. Job duties:
- Interface with other departments to solve production and technical problems.
- Advanced subject matter expertise for engineering change orders, non-conforming reports, and material review boards.
- Identify and implement new laboratory equipment and processes.
- Perform, interpret, and report analytical testing.
- Evaluate, create, and initiate improvements to existing engineering, project, and departmental systems.
- Oversee junior chemists’ execution of equipment and processes validations.
- Review, modify, and develop documents such as build of materials, manufacturing procedures, test methods and reports, validations, failure modes/effects analyses, etc.
- Guide junior chemists in their support of prototype and pilot production, facilities, planning, and process knowledge transfer.
- Advise team members on existing manufacturing processes, new products, product changes, and enhancements, as well as related tooling and fixtures.
- Supervise supporting manufacturing technicians or associates as needed.
- Day-to-day tasks performed under little to no supervision.
- Perform other duties as assigned (e.g., create presentations, reports, etc.).
Qualifications
- Bachelor’s degree in Chemistry, Chemical Sciences, or a related field of study.
- A minimum of six (6) to eight (8) years of relevant industrial experience in chemical synthesis and materials analysis, or equivalent combination of advanced degree and relevant experience.
- Strong written and verbal communication skills.
- Previous experience directing junior chemists’ work.
- Proficient computer skills including Microsoft Office Suite: Excel, PowerPoint, Outlook, Word, and Teams.
Desired Qualifications
- Ability to read and prepare technical documentation.
- Extensive knowledge of laboratory equipment, organic-synthetic and transformation processes, test methods, and qualitative and quantitative measurements.
- Knowledge of the medical device space, pharmaceuticals, or similar industry.
- Lean/Six Sigma Yellow/Green/Black Belt certifications or equivalent.
About Terumo Neuro
Terumo Neuro develops and commercializes catheter-based, minimally invasive medical devices for neurovascular conditions, including cerebral aneurysms, ischemic stroke, carotid artery disease, and neurovascular malformations. Formerly MicroVention, the company became Terumo Neuro in 2024 and now offers more than 30 products focused on advancing physician practice and patient outcomes.
Why Join
- Specializes in minimally invasive neuroendovascular technologies designed to preserve and restore brain health.
- Expanded from its original focus on aneurysm therapy to solutions for ischemic stroke, carotid artery disease, and neurovascular malformations.
- Supported by a global community of more than 3,800 engineers, chemists, marketers, manufacturers, researchers, and innovators.
- Maintains extensive clinical research capabilities, including more than 40 years of pre- and post-market neurovascular research.
Skills & Tech
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