As a Senior R&D Engineer you will develop new technology, products, materials, processes, or equipment with minimal supervision. Independently, or as a member of a team, develops, directs, and executes plans for a major segment of complex projects. Compiles and analyzes operational, test, and research data to establish technical specifications for designing or modifying products, processes, and materials.

Key Responsibilities:

• Lead or support workstream activities on Next Generation calcium products ensuring product safety, compliance and performance improvements.
• Support marketing in gathering customer feedback on next generation products.
• Product demonstrations at conferences
• Early conceptual work as part of exploratory in the calcium space
• Development of pilot processes and equipment, Process Design and Development, preparation of specifications, process capability studies, six sigma process testing, report preparation, process/test documentation, transfer of processes from pilot to manufacturing.
• Work independently to plan and schedule own activities necessary to meet timelines.
• Lead or participate in a cross functional team to perform troubleshooting on new products/process problems as related to design, material or process.
• Summarize, analyse, and draw conclusions from test results.
• Prepare standard reports/documentation to communicate results to technical community.
• Be responsible for engineering documentation.
• Train and/or provide work direction/supervision to technicians.
• Work co-operatively with process development, quality, manufacturing, regulatory, clinical and marketing to ensure project success.
• Communicate changes in project milestones and write project reports as required.
• As a member of the development team you will have significant impact working within the development process to bring product/process through from concept to commercialisation applying Exploratory, Technical Development Process (TDP) and Product Development Process (PDP) methodologies.
• Ability to provide technical guidance within a large team and be an effective communicator within a multidisciplinary and international organization.
• Evaluate in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
• Ensure regulatory compliance to GMP’s of all medical device regulatory agencies (e.g., FDA, ISO and MDD).
• Flexibility to travel to US and Europe What we’re looking for:

Requirements:

• Bachelor’s level 8 degree (240 credits), in a scientific or engineering discipline (STEM) preferably Mechanical or Biomedical.
• Minimum 6 years experience preferably in R&D.
• Availability for international travel when required.